← Compound index
COMPOUND RECORD / VESUGEN

VesugenВезуген

RecoveryPerformance
Source linked

What the studies found

Observational study · 2013

Vezugen in postoperative chronic lower-limb arterial insufficiency

Clinical and blood-flow findings
Qualitative improvement reported; numerical effects and a comparator arm not established.

Clinical and ultrasound blood-flow improvement was reported after Vezugen treatment; the abstract supplies no numerical effect estimate.

Study notes · methods, sources and limitations

Participants or model 41 postoperative patients with chronic lower-limb ischemia

Design 41 postoperative patients; before/after clinical and ultrasound assessment of Vezugen treatment.

Important limitations

  • No control arm, masking or numerical treatment effect established from the abstract. Distinct from PMID 25051774 (2014); participant overlap remains unresolved. The findings apply to the preparation tested. Efficacy of purified KED remains uncertain.
  • Separate 2013 publication; overlap with the 2014 erectile-dysfunction report is unresolved.

Advances in Gerontology / Uspekhi Gerontologii. 2013;26(2):292–296. PMID 28976154 · Original clinical journal publication

Original source or citation ↗

Study results and tables ↗

Animal research · 2008

Vesugen in the separate adult-hypoxia arm

Study of multiple preparations

Respiration arrest
88 ± 9 secondsSaline 72 ± 10 seconds; n=10/groupNo numerical p-value supplied
Adult mortality
10%Saline 10%; very small groups, no verified mortality difference test

In adult male rats, Vesugen was associated with 88 ± 9 seconds to respiration arrest versus 72±10 with saline. This arm did not expose pregnant animals to Vesugen.

Study notes · methods, sources and limitations

Participants or model Pregnant rats exposed to hypoxia on gestation day 10; separate adult-male experiment, n=10/group; offspring open-field strata n=6, 11, 9 and 12

Design Two distinct experiments: five-day pretreatment in adult males, and maternal Pinealon after gestation-day-10 hypoxia. Offspring cerebellar cells tested at day 12; open-field behavior at four weeks, stratified by maternal hypoxia sensitivity.

Important limitations

  • Only Pinealon was studied in the maternal arm of this publication. Adult hypoxia findings are adjacent context, not pregnancy-safety evidence.
  • Animal injury experiments do not establish human pregnancy safety. Epitalon, Vilon and Vesugen were tested only in the adult-male arm of this paper. Number of pregnant dams, randomization, masking and litter-adjusted statistics are not established. Offspring are not independent maternal exposures. Table 1 mortality conflicts with the prose; do not convert the latter into a verified excess risk. Vilon and Epitalon respiration findings marked p<0.08 are not demonstrated p<0.05 results. The paper prints an Epitalon sequence ending in Arg; established Epitalon identity is Ala-Glu-Asp-Gly. That apparent source error is retained as an identity warning.

Doklady Biological Sciences. 2008;418:7–10; Russian original Doklady Akademii Nauk 418(3):419–422. PMID 21249538 · Original journal publication

Original source or citation ↗

Source for the reported results ↗

Study results and tables ↗

Comparison in people · 2012

Peptide combinations investigated in professional drivers

Study of multiple preparations

Sociodemographic associations
Not statistically significantp>0.1
Peptide-associated psychoemotional/adaptation changes
Statistically significant range reportedp<0.001–0.05
Preferred combination in the authors’ report
Pinealon + VesugenSeparate treatment-arm sizes and absolute outcome changes not stated

The abstract describes occupational psychoemotional differences and reports changes with peptide bioregulators, including combined Pinealon and Vezugen.

Study notes · methods, sources and limitations

Participants or model 150 male lorry drivers and 150 male metal craftsmen in the occupational comparison

Design 150 male lorry drivers (43.3 ± 0.9 years) and 150 male metal craftsmen (42.8 ± 0.9 years); three psychological-adaptation categories.

Important limitations

  • The 300-person occupational comparison is not a verified treatment-group size; Pinealon and Vesugen were combined.
  • The occupational cohort size is not a verified randomized-treatment sample size. Randomization, blinding, and intervention-group sizes are not established from the abstract. Combination findings do not identify either peptide’s independent contribution or demonstrate fewer driving accidents.
  • The 300-person occupational comparison is not a verified randomized-treatment denominator.

Adv Gerontol. 25(4):718–728 · Indexed abstract

Original source or citation ↗

Study results and tables ↗
01 / OVERVIEW

About Vesugen

Names in this research collection

KED · Vezugen

Vesugen is the KED tripeptide (Lys–Glu–Asp) in the short-peptide catalogue, studied in vascular and cell-aging research. It is not the whole vessel extract Vasolin/Slavinorm.

Identity / background source ↗

Research background

A peptide research entry in the Khavinson evidence map. Direct studies, related extract findings, institute reports and unresolved claims are distinguished below.

Autoimmune research: disease-specific findings, immune effects and open questions ↗

Pregnancy and offspring research

In adult male rats, Vesugen was associated with 88 ± 9 seconds to respiration arrest versus 72±10 with saline. This arm did not expose pregnant animals to Vesugen.

Only Pinealon was studied in the maternal arm of this publication. Adult hypoxia findings are adjacent context, not pregnancy-safety evidence.

Reported findings and methods ↗ · Pregnancy research: full evidence review and archive ↗

More study findings

Observational study · 2015

Aging-marker changes included mixed signals

Study of multiple preparations

Biological-age indicators
Authors reported favorable changes after Pinealon or Vesugen; comparative effect size unavailable
Oxidation and blood-cell markers
Prooxidant activity and lower circulating CD34-positive markers also reported

The authors reported changes in biological-age indicators after Pinealon and Vesugen. They also reported prooxidant activity and lower circulating CD34-positive cell markers.

Study notes · methods, sources and limitations

Participants or model Adults aged 41–83 with multiple conditions and organic brain syndrome in remission

Design Adults aged 41–83 with multiple conditions and organic brain syndrome in remission; Pinealon and Vesugen studied.

Printed total enrollment
32
Printed sex breakdown
18 men + 12 women = 30; does not reconcile with printed total

Important limitations

  • The reported total does not match the sex breakdown. Pinealon-specific effects cannot be separated from the available report.
  • The abstract states 32 participants but lists 18 men and 12 women; the reported participant totals differ. Allocation, comparator details and preparation-specific effects require the full paper. The biomarker findings do not establish clinical harm, longevity benefit or genetic safety; favorable author conclusions should not erase the adverse-direction signals.
  • The abstract says 32 participants while listing 18 men and 12 women. It does not isolate preparation-specific effects or establish longevity, genetic safety or clinical harm.

Advances in gerontology = Uspekhi gerontologii; 2015 · Indexed abstract

Original source or citation ↗

Study results and tables ↗

Observational study · 2016

Personified prevention of diseases under the conditions of the Far North

Study of multiple preparations

Sick-leave certificates
18 → 102014 → 2015; whole program
Days unfit for work
119 → 602014 → 2015; whole program
Seasonal morbidity
No statistically reliable improvement reported

A personalized multi-preparation program recorded 18 → 10 sick-leave certificates and 119 → 60 days unfit for work between 2014 and 2015. The paper found no statistically reliable seasonal-morbidity improvement.

More reported outcomes
Narrative/table discrepancy
Narrative 43.4% decrease; Table 2 gives 119 → 60 daysUnresolved source discrepancy; not interchangeable figures
Study notes · methods, sources and limitations

Participants or model 113 Gazprom Dobycha Urengoy employees (74 men, 39 women), assessed in 2015; comparison with the preceding year, without a concurrent control.

Design 113 Gazprom Dobycha Urengoy employees (74 men, 39 women), assessed in 2015; comparison with the preceding year, without a concurrent control.

Important limitations

  • One shared cohort, not a separate trial for each named preparation. Genotype-guided assignments and other care prevent isolating a product effect. The narrative reports a 43.4% reduction, which does not reconcile with the table’s 119 → 60 days. The background 11,000-worker claim is not this cohort.

Vrach. 2016;(6):64–66 · Journal publication

Original source or citation ↗

Study results and tables ↗

Lab research · 2012

Peptides tissue-specifically stimulate cell differentiation during their aging

Study of multiple preparations

Differentiation markers
CXCL12/Hoxa3 or CXCL12/WEGC1 expression increased in the corresponding cultures

Pancragen increased differentiation-marker expression in pancreatic cells, Bronchogen in bronchial cells, and Vesugen in prostatic fibroblasts. Responses were more pronounced in aged cultures.

Study notes · methods, sources and limitations

Participants or model Human embryonic pancreatic and bronchial cell cultures, plus human prostatic fibroblasts, compared at different passage ages.

Design Human embryonic pancreatic and bronchial cell cultures, plus human prostatic fibroblasts, compared at different passage ages.

Preparation assignments
Pancragen KEDW → pancreas; Bronchogen AEDL → bronchial cells; Vesugen KED → prostatic fibroblasts

Important limitations

  • Different peptides were tested in different cell types; this is not a combination trial or evidence of organ recovery in patients. No numerical effect sizes are supplied.

Bulletin of experimental biology and medicine 2012 · Journal publication

Original source or citation ↗

Study results and tables ↗

Review of earlier studies · 2026

Review connects vascular extracts, KED and AEDR experimental research

Study of multiple preparations

Preparations reviewed
Vascular polypeptide preparation, KED and AEDR
Endothelial findings
KED restored elevated ET-1 expression toward normal in reported culturesCultures derived from patients are not a clinical treatment trial
Cardiac findings
AEDR experimental cardioprotection summarizedAnimal experiments; no new human trial

The review brings together vascular polypeptide, KED and AEDR research. It describes changes in endothelial endothelin-1 expression, vascular hemodynamics and experimental myocardial injury. These preparation-specific observations are preclinical; the review supplies no new human cardiovascular efficacy trial.

Study notes · methods, sources and limitations

Participants or model Review of vascular-polypeptide, KED and AEDR experiments in endothelial cultures and animal cardiovascular models.

Important limitations

  • Review of earlier experiments, not independent replication. Vascular extracts, KED and AEDR are different preparations; effects cannot be transferred between them. Exact publication day is not supplied by the index; newly indexed 28 October 2026.

Advances in gerontology = Uspekhi gerontologii 39(4) · Journal publication

Original source or citation ↗

Study results and tables ↗

Research updates ↗

Compound class
Bioregulator
Research collection
Peptide bioregulation · editorial grouping
Research institutions
No institutional affiliation recorded
Source review
Review dates and the material assessed are listed with each publication below.
02 / HOW TO READ THE RESEARCH

Understanding the evidence

Human research

Original human reports linked; methods and cohort overlap need appraisal

Study methods

Abstract-level review

Independent replication

Independent replication not established by this collection

Source access

See source-specific abstracts, institute reports and explicit review scopes

Safety evidence

Incomplete assessment; findings do not establish safety for personal use

Open a topic for the evidence assessment.

More findings, background and history

What remains unclear

Overlap between the 2013 and 2014 postoperative reports remains unclear. The 2015 Pinealon and Vesugen report lists 32 participants but gives a breakdown of 18 men and 12 women. The report also leaves treatment-arm attribution for oxidative and CD34 marker changes unclear.

Human reports are linked; their presence does not establish effectiveness. Several publications can describe the same participants.

Browse original study records ↗
PEPTIDE RESEARCH / OCT 2026

Related preparations and evidence

Evidence belongs to the preparation actually studied. A tissue extract and a synthetic peptide can belong to the same research tradition without having equivalent effects or safety.

Blood vessels: the molecular link

Vasolin / Slavinorm → Vesugen / KED

KED was detected in vessel complex in the 2020 composition paper. Vesugen is the KED short-peptide entry; the separate KED route preserves sequence-based research navigation.

Clinical evidence and limitations

Original vessel-complex records now include 108-person arterial and 190-person venous randomized trials plus separate comparisons. These do not isolate Vesugen or purified KED.

Retrieve complete randomized papers and confirm the preparation in unnamed abstracts. Same sequence does not establish equivalence of complex preparations or clinical effects for purified KED.

Related preparations

Some references concern related extracts, reviews or molecular identification rather than direct studies of this compound.

Explore the full bioregulator collection ↗

View this preparation in the Khavinson evidence map ↗

PATENT RESEARCH / COLLECTION UPDATED 7 NOVEMBER 2026

Patents and claimed inventions

These 3 grouped records distinguish claimed molecules, uses, formulations and related chemistry. Patent disclosure does not establish clinical benefit or approval.

2016 · RU2582976C1 · Vesugen plus Chonsurid: dental bone-healing methodUse · 21 mm defect: healing at 4.5 months; regenerate density 200 HU

Reported findings

The Vesugen example reports earlier radiographic healing and greater regenerate density, in a different patient and defect.

Vesugen adjunct case
21 mm defect: healing at 4.5 months; regenerate density 200 HUOne 65-year-old patient
Chonsurid-only example
19 mm defect: healing at 6 months; regenerate density 175 HUOne 62-year-old patient
All reported results, comparisons and limitations →

Use. The method combines branded Vesugen with Chonsurid and dental care.

This is a combination-care claim; it does not establish the independent effect of purified KED or a general bone-healing benefit.

Publication
RU2582976C1 ↗ · 2016-04-27
Earliest priority / filing
2014-10-20 / 2014-10-20
Original applicant / assignee
Андрей Константинович Иорданишвили
Indexed status
Not shown; official status unverified · checked 2026-11-06
Patent family
55794784 · family publications are related filings, not independent studies.
Original title, inventors and related publications

Method of accelerating process of reparative osteogenesis

Inventors: Андрей Константинович Иорданишвили; Антон Анатольевич Сериков; Дмитрий Викторович Балин; Анна Геннадьевна Слугина; Владимир Владимирович Самсонов; Борис Лаврович Макеев; Сергей Константинович Осмоловский.

RU2582976C1

Original patent PDF ↗

Read source review →

2015 · RU2554504C1 · Vesugen: salivary-function adjunctive methodUse · Saliva collected over 20 minutes: 1.6 → 2.34 mL

Reported findings

Both cases reported more saliva after 30 days; the Vesugen case had the larger numerical increase.

Conventional-care case
Saliva collected over 20 minutes: 1.6 → 2.34 mL30 daysOne 60-year-old patient
Vesugen adjunct case
Saliva collected over 20 minutes: 1.3 → 4.3 mL30 daysOne 65-year-old patient receiving several treatments
All reported results, comparisons and limitations →

Use. This method describes branded Vesugen during treatment of drug-associated salivary dysfunction.

Branded tablets and concurrent treatment are not evidence for isolated KED, and patent examples may overlap clinical reports.

Publication
RU2554504C1 ↗ · 2015-06-27
Earliest priority / filing
2014-02-20 / 2014-02-20
Original applicant / assignee
Андрей Константинович Иорданишвили; Валерий Валерьевич Лобейко
Indexed status
Not shown; official status unverified · checked 2026-11-06
Patent family
53498546 · family publications are related filings, not independent studies.
Original title, inventors and related publications

Method of treating drug sialoadenopathy

Inventors: Андрей Константинович Иорданишвили; Валерий Валерьевич Лобейко.

RU2554504C1

Original patent PDF ↗

Read source review →

2010 · US7851449B2 · KED / Vesugen: defined peptide and microcirculation claimsMolecule · Treated group III–IV → II; control III–IV → III–IV

Reported findings

The patent reports improved cuff-test resistance and changes in coagulation measures after ten days.

Cuff test
Treated group III–IV → II; control III–IV → III–IV10-day courseOrdinal capillary-resistance measure
Recalcification time
164.2 ± 2.4 with KED versus 147.3 ± 4.2 controlHealthy comparison value 178.0 ± 14.0; not a clinical vascular event
All reported results, comparisons and limitations →

Molecule. The granted claims explicitly identify H-Lys-Glu-Asp-OH and compositions or methods involving microcirculation disorders.

Defined KED is not automatically identical to a branded multicomponent capsule or vascular tissue extract.

Publication
US7851449B2 ↗ · 2010-12-14
Earliest priority / filing
2006-05-23 / 2006-12-04
Original applicant / assignee
SIA Peptides OOO
Indexed status
Active - Reinstated · checked 2026-11-06
Patent family
37999085 · family publications are related filings, not independent studies.
Original title, inventors and related publications

Peptide, pharmaceutical composition, and a method of treating microcirculation disorders

Inventors: Vladimir Khatskelevich Khavinson; Evgeny Iosifovich Grigoriev; Vladimir Victorovich Malinin; Galina Anatolievna Ryzhak.

US7851449B2 · EP2024387B1 · KR20090009867A · ATE446309T1 · DE602006009976D1 · DK2024387T3 · EA010158B1 · IL194500A · RU2295970C1 · UA91137C2 · WO2007136294A1

Original patent PDF ↗

Read source review →

Status is an indexed snapshot, not an official legal assessment. Search the patent collection and read the method →

03 / SOURCE RECORDS

Linked sources

Explore the research map and unresolved leads ↗

2008 · Pinealon after maternal hypoxia: offspring and adult-rat findingsOffspring per dam: 14 ± 2 versus 9 ± 3
2008Animal / experimentalFull text available

Pinealon after maternal hypoxia: offspring and adult-rat findings

Pinealon in maternal arm; separate adult-male Vilon, Vesugen, Pinealon and Epitalon arms · Original journal publication

Format: Original PDF · Reviewed: Original four-page PDF; methods and Tables 1–2 visually verified, printed pp.7–9. Journal year 2008, despite later index date.

L. S. Kozina, A. V. Arutjunyan, S. L. Stvolinskii, M. S. Stepanova, M. G. Makletsova, V. Kh. Khavinson · Doklady Biological Sciences. 2008;418:7–10; Russian original Doklady Akademii Nauk 418(3):419–422. PMID 21249538

Pinealon-treated hypoxic dams had 14±2 offspring versus 9±3 with saline (p<0.05). Offspring activity and neuronal responses changed. Adult-rat Table 1 reports 10% mortality with both Pinealon and saline, conflicting with the narrative claim of higher Pinealon mortality.

Results and tables

Reported findings and study design

Reported findings

Pinealon-treated hypoxic dams had 14±2 offspring versus 9±3 with saline (p<0.05). Offspring activity and neuronal responses changed. Adult-rat Table 1 reports 10% mortality with both Pinealon and saline, conflicting with the narrative claim of higher Pinealon mortality.

Two distinct experiments: five-day pretreatment in adult males, and maternal Pinealon after gestation-day-10 hypoxia. Offspring cerebellar cells tested at day 12; open-field behavior at four weeks, stratified by maternal hypoxia sensitivity.

Dose, route and schedule

Maternal experiment: hypoxia on gestation day 10, then Pinealon 10 µg/kg intraperitoneally on five alternate days; saline comparator. Adult males: each peptide 10 µg/kg/day intraperitoneally for five days before hypoxia. These are distinct experimental schedules, not human-use instructions.

Protocol source ↗ · Original four-page PDF; methods and Tables 1–2 visually verified, printed pp.7–9. Journal year 2008, despite later index date.

Results · Original four-page PDF; methods and Tables 1–2 visually verified, printed pp.7–9. Journal year 2008, despite later index date.
MeasureResultComparison, timing and statistics
Offspring per dam14 ± 2 versus 9 ± 3Pinealon after maternal hypoxia versus saline · Birth · p<0.05; number of dams and meaning of ± not explicitly supplied
Horizontal activity, offspring of sensitive dams53 ± 5.1 versus 36 ± 6.9n=11 versus n=6 offspring · Four weeks · p<0.05
Adult-male respiration arrest184 ± 30 versus 72 ± 10 secondsPinealon versus saline; n=10/group · After five-day pretreatment · p<0.014
Adult mortality: table versus proseTable 1: saline 10%, Pinealon 10%, Vilon 20%, Vesugen 10%, Epitalon 20%Narrative says higher mortality with Pinealon; discrepancy unresolved
Oxidative readoutsLower cell death did not consistently correspond to lower ROSH₂O₂ and NMDA responses differed; exact figure bars not digitized
Adult-male arm: Table 1, n=10/group
Adult-male arm: Table 1, n=10/group
GroupTime to respiration arrest (s)Posture recovery (s)Restitution (s)Restitution coefficientMortality (%)
Saline72 ± 10126 ± 21202 ± 322.810
Vilon149 ± 47 (p<0.08)152 ± 31302 ± 50 (p<0.08)2.020
Vesugen88 ± 9111 ± 16194 ± 242.210
Pinealon184 ± 30 (p<0.014)152 ± 16291 ± 35 (p<0.1)1.610
Epitalon150 ± 38 (p<0.08)103 ± 28185 ± 331.220

Printed p-values compare saline. Unmarked cells have no numerical p-value supplied. Uncertainty type is not clearly defined. This is not a pregnancy-outcome table.

Offspring open-field Table 2: significant activity outcomes
Offspring open-field Table 2: significant activity outcomes
MeasureSensitive dams, saline offspring (n=6)Sensitive dams, Pinealon offspring (n=11)Resistant dams, saline offspring (n=9)Resistant dams, Pinealon offspring (n=12)
Horizontal activity36 ± 6.953 ± 5.145 ± 3.357 ± 3.3
Vertical activity2 ± 0.85 ± 0.82 ± 0.66 ± 1.1

Both Pinealon comparisons marked p<0.05 against the corresponding hypoxic untreated stratum. Increased activity is not itself evidence of better memory or normal development.

Animal injury experiments do not establish human pregnancy safety. Epitalon, Vilon and Vesugen were tested only in the adult-male arm of this paper. Number of pregnant dams, randomization, masking and litter-adjusted statistics are not established. Offspring are not independent maternal exposures. Table 1 mortality conflicts with the prose; do not convert the latter into a verified excess risk. Vilon and Epitalon respiration findings marked p<0.08 are not demonstrated p<0.05 results. The paper prints an Epitalon sequence ending in Arg; established Epitalon identity is Ala-Glu-Asp-Gly. That apparent source error is retained as an identity warning.

Source for these results ↗ · Reviewed 2026-11-08

Population / setting
Pregnant rats exposed to hypoxia on gestation day 10; separate adult-male experiment, n=10/group; offspring open-field strata n=6, 11, 9 and 12
Source reviewed
Original four-page PDF; methods and Tables 1–2 visually verified, printed pp.7–9. Journal year 2008, despite later index date.
Study limitations
  • Animal injury experiments do not establish human pregnancy safety. Epitalon, Vilon and Vesugen were tested only in the adult-male arm of this paper.
  • Number of pregnant dams, randomization, masking and litter-adjusted statistics are not established. Offspring are not independent maternal exposures.
  • Table 1 mortality conflicts with the prose; do not convert the latter into a verified excess risk. Vilon and Epitalon respiration findings marked p<0.08 are not demonstrated p<0.05 results.
  • The paper prints an Epitalon sequence ending in Arg; established Epitalon identity is Ala-Glu-Asp-Gly. That apparent source error is retained as an identity warning.

Reviewed 2026-11-08.

Read the source ↗
2016 · Vesugen plus Chonsurid: dental bone-healing method — RU2582976C1Vesugen adjunct case: 21 mm defect: healing at 4.5 months; regenerate density 200 HU
2016Patent / reported experimentsFull text available

Vesugen plus Chonsurid: dental bone-healing method — RU2582976C1

Patent-defined substance or composition · Patent publication

Format: Original patent text and indexed metadata · Reviewed: Claims, selected reported findings and limitations reviewed; supporting experiments not comprehensively appraised.

Андрей Константинович Иорданишвили, Антон Анатольевич Сериков, Дмитрий Викторович Балин, Анна Геннадьевна Слугина, Владимир Владимирович Самсонов, Борис Лаврович Макеев, Сергей Константинович Осмоловский · RU2582976C1 · patent family 55794784

The Vesugen example reports earlier radiographic healing and greater regenerate density, in a different patient and defect.

Results and tables

Reported patent results

Reported findings

The Vesugen example reports earlier radiographic healing and greater regenerate density, in a different patient and defect.

Two dental-cyst case examples after surgery and Chonsurid filling, with or without preoperative branded Vesugen.

Results · Description: clinical observations 1 and 2.
MeasureResultComparison, timing and statistics
Vesugen adjunct case21 mm defect: healing at 4.5 months; regenerate density 200 HUOne 65-year-old patient
Chonsurid-only example19 mm defect: healing at 6 months; regenerate density 175 HUOne 62-year-old patient

Individual defects and patients differ. These are not randomized groups, and the independent effect of Vesugen or purified KED cannot be determined.

Source for these results ↗ · Reviewed 2026-11-06

Population / setting
Two dental-cyst case examples after surgery and Chonsurid filling, with or without preoperative branded Vesugen.
Source reviewed
Original patent publication accessed through Google Patents. Claims, selected reported findings and source limitations checked. The results section identifies the examples, tables and any numerical extraction gaps. No complete experimental audit, prosecution review or legal claim construction was performed.
Study limitations
  • This is a combination-care claim; it does not establish the independent effect of purified KED or a general bone-healing benefit.
  • Individual defects and patients differ. These are not randomized groups, and the independent effect of Vesugen or purified KED cannot be determined.
  • Patents record claimed inventions and supporting disclosures. Publication or grant does not establish clinical efficacy, safety or marketing approval. Members of one patent family and related journal reports can describe the same experiments.
  • Status labels are Google Patents index snapshots for the displayed publication or application; each record lists the review date. Official registers and every national family member have not been independently checked. These labels do not establish freedom to operate.

Reviewed 2026-11-06.

Read the source ↗
2015 · Vesugen: salivary-function adjunctive method — RU2554504C1Conventional-care case: Saliva collected over 20 minutes: 1.6 → 2.34 mL
2015Patent / reported experimentsFull text available

Vesugen: salivary-function adjunctive method — RU2554504C1

Patent-defined substance or composition · Patent publication

Format: Original patent text and indexed metadata · Reviewed: Claims, selected reported findings and limitations reviewed; supporting experiments not comprehensively appraised.

Андрей Константинович Иорданишвили, Валерий Валерьевич Лобейко · RU2554504C1 · patent family 53498546

Both cases reported more saliva after 30 days; the Vesugen case had the larger numerical increase.

Results and tables

Reported patent results

Reported findings

Both cases reported more saliva after 30 days; the Vesugen case had the larger numerical increase.

Two different patients with chemotherapy-associated dry mouth: conventional care in one case and conventional care plus branded Vesugen in the other.

Results · Description: Examples 1 and 2.
MeasureResultComparison, timing and statistics
Conventional-care caseSaliva collected over 20 minutes: 1.6 → 2.34 mLOne 60-year-old patient · 30 days
Vesugen adjunct caseSaliva collected over 20 minutes: 1.3 → 4.3 mLOne 65-year-old patient receiving several treatments · 30 days

Different patients, cancer locations and baseline values make this an illustrative comparison, not a controlled estimate. Branded capsules do not establish isolated KED efficacy.

Source for these results ↗ · Reviewed 2026-11-06

Population / setting
Two different patients with chemotherapy-associated dry mouth: conventional care in one case and conventional care plus branded Vesugen in the other.
Source reviewed
Original patent publication accessed through Google Patents. Claims, selected reported findings and source limitations checked. The results section identifies the examples, tables and any numerical extraction gaps. No complete experimental audit, prosecution review or legal claim construction was performed.
Study limitations
  • Branded tablets and concurrent treatment are not evidence for isolated KED, and patent examples may overlap clinical reports.
  • Different patients, cancer locations and baseline values make this an illustrative comparison, not a controlled estimate. Branded capsules do not establish isolated KED efficacy.
  • Patents record claimed inventions and supporting disclosures. Publication or grant does not establish clinical efficacy, safety or marketing approval. Members of one patent family and related journal reports can describe the same experiments.
  • Status labels are Google Patents index snapshots for the displayed publication or application; each record lists the review date. Official registers and every national family member have not been independently checked. These labels do not establish freedom to operate.

Reviewed 2026-11-06.

Read the source ↗
2010 · KED / Vesugen: defined peptide and microcirculation claims — US7851449B2Cuff test: Treated group III–IV → II; control III–IV → III–IV
2010Patent / reported experimentsFull text available

KED / Vesugen: defined peptide and microcirculation claims — US7851449B2

Patent-defined substance or composition · Patent publication

Format: Original patent text and indexed metadata · Reviewed: Claims, selected reported findings and limitations reviewed; supporting experiments not comprehensively appraised.

Vladimir Khatskelevich Khavinson, Evgeny Iosifovich Grigoriev, Vladimir Victorovich Malinin, Galina Anatolievna Ryzhak · US7851449B2 · patent family 37999085

The patent reports improved cuff-test resistance and changes in coagulation measures after ten days.

Results and tables

Reported patent results

Reported findings

The patent reports improved cuff-test resistance and changes in coagulation measures after ten days.

Purpura-senilis patent comparison in 23 people aged 70–82: 12 receiving KED and 11 saline; the text states random division.

Results · Clinical example and Tables 2–3; control and healthy-reference values retained.
MeasureResultComparison, timing and statistics
Cuff testTreated group III–IV → II; control III–IV → III–IVOrdinal capillary-resistance measure · 10-day course · p<0.05 before/after in treated group
Recalcification time164.2 ± 2.4 with KED versus 147.3 ± 4.2 controlHealthy comparison value 178.0 ± 14.0; not a clinical vascular event · p<0.05 versus control
Activated partial thromboplastin time58.9 ± 0.7 versus 48.0 ± 1.3 seconds; healthy reference 32.3 ± 2.1The treated value moves further from this reference; not every measure is normalized

Very small patent comparison, with masking and allocation concealment unverified. Laboratory changes do not establish clinical prevention, and the source’s normalization language overstates at least one displayed measure.

Source for these results ↗ · Reviewed 2026-11-06

Population / setting
Purpura-senilis patent comparison in 23 people aged 70–82: 12 receiving KED and 11 saline; the text states random division.
Source reviewed
Original patent publication accessed through Google Patents. Claims, selected reported findings and source limitations checked. The results section identifies the examples, tables and any numerical extraction gaps. No complete experimental audit, prosecution review or legal claim construction was performed.
Study limitations
  • Defined KED is not automatically identical to a branded multicomponent capsule or vascular tissue extract.
  • Very small patent comparison, with masking and allocation concealment unverified. Laboratory changes do not establish clinical prevention, and the source’s normalization language overstates at least one displayed measure.
  • Patents record claimed inventions and supporting disclosures. Publication or grant does not establish clinical efficacy, safety or marketing approval. Members of one patent family and related journal reports can describe the same experiments.
  • Status labels are Google Patents index snapshots for the displayed publication or application; each record lists the review date. Official registers and every national family member have not been independently checked. These labels do not establish freedom to operate.

Reviewed 2026-11-06.

Read the source ↗
2013 · Vezugen in postoperative chronic lower-limb arterial insufficiencyClinical and blood-flow findings: Qualitative improvement reported; numerical effects and a comparator arm not established.
2013Uncontrolled human reportEnglish abstract

Vezugen in postoperative chronic lower-limb arterial insufficiency

Vezugen; exact formulation/sequence not established by abstract · Original clinical journal publication

Format: Original indexed abstract · Reviewed: Europe PMC indexed abstract and metadata checked

K. V. Kitachov, A. D. Sazonov, K. L. Kozlov, K. Yu. Petrov, A. S. Slusarev, E. V. Sedova · Advances in Gerontology / Uspekhi Gerontologii. 2013;26(2):292–296. PMID 28976154

Clinical and ultrasound blood-flow improvement was reported after Vezugen treatment; the abstract supplies no numerical effect estimate.

Results and tables

Reported findings and study design

41 postoperative patients; before/after clinical and ultrasound assessment of Vezugen treatment.

Results · Original indexed English abstract, PMID 28976154
MeasureResultComparison, timing and statistics
Clinical and blood-flow findingsQualitative improvement reported; numerical effects and a comparator arm not established.

Separate 2013 publication; overlap with the 2014 erectile-dysfunction report is unresolved.

Source for these results ↗ · Reviewed 2026-11-06

Population / setting
41 postoperative patients with chronic lower-limb ischemia
Source reviewed
Indexed English abstract; full article not recovered.
Study limitations
  • No control arm, masking or numerical treatment effect established from the abstract.
  • Distinct from PMID 25051774 (2014); participant overlap remains unresolved.
  • The findings apply to the preparation tested. Efficacy of purified KED remains uncertain.

Reviewed 2026-11-06.

Read the source ↗
2016 · Personified prevention of diseases under the conditions of the Far NorthSick-leave certificates: 18 → 10
2016Uncontrolled human reportFull text available

Personified prevention of diseases under the conditions of the Far North

Risk-assigned capsule program: Endoluten tissue extract and named synthetic peptide products; Cerluten also named in assignments · Journal publication

S. Trofimova, A. Trofimov, A. Koryakin, A. Chubukin, V. Ternovoy · Vrach. 2016;(6):64–66

A personalized multi-preparation program recorded 18 → 10 sick-leave certificates and 119 → 60 days unfit for work between 2014 and 2015. The paper found no statistically reliable seasonal-morbidity improvement.

Results and tables

Reported findings and study design

A personalized multi-preparation program recorded 18 → 10 sick-leave certificates and 119 → 60 days unfit for work between 2014 and 2015. The paper found no statistically reliable seasonal-morbidity improvement.

113 Gazprom Dobycha Urengoy employees (74 men, 39 women), assessed in 2015; comparison with the preceding year, without a concurrent control.

Dose, route and schedule

One capsule of the assigned preparation daily for 20 days. Products were selected by risk assessment; all six products were not given to every participant.

Protocol source ↗ · Original PDF p.65

Results · Original publisher PDF pp.64–66; Table 2 visually checked
MeasureResultComparison, timing and statistics
Sick-leave certificates18 → 102014 → 2015; whole program
Days unfit for work119 → 602014 → 2015; whole program
Seasonal morbidityNo statistically reliable improvement reported
Narrative/table discrepancyNarrative 43.4% decrease; Table 2 gives 119 → 60 daysUnresolved source discrepancy; not interchangeable figures
Table 2 · Chronic-disease recurrence-related sick leave
Table 2 · Chronic-disease recurrence-related sick leave
Measure20142015
Sick-leave certificates1810
Days unfit for work11960

Historical comparison for the shared 113-worker program. Not preparation-specific results.

One shared cohort, not a separate trial for each named preparation. Genotype-guided assignments and other care prevent isolating a product effect. The narrative reports a 43.4% reduction, which does not reconcile with the table’s 119 → 60 days. The background 11,000-worker claim is not this cohort.

Source for these results ↗ · Reviewed 2026-11-01

Population / setting
113 Gazprom Dobycha Urengoy employees (74 men, 39 women), assessed in 2015; comparison with the preceding year, without a concurrent control.
Source reviewed
Original publisher PDF methods and clinical table checked; table visually verified.
Study limitations
  • One shared cohort, not a separate trial for each named preparation. Genotype-guided assignments and other care prevent isolating a product effect. The narrative reports a 43.4% reduction, which does not reconcile with the table’s 119 → 60 days. The background 11,000-worker claim is not this cohort.

Reviewed 2026-11-01.

Read the source ↗
2012 · Peptides tissue-specifically stimulate cell differentiation during their agingDifferentiation markers: CXCL12/Hoxa3 or CXCL12/WEGC1 expression increased in the corresponding cultures
2012In vitroEnglish abstract

Peptides tissue-specifically stimulate cell differentiation during their aging

Defined synthetic peptides · Journal publication

Khavinson VKh, Linkova NS, Polyakova VO, Kheifets OV, Tarnovskaya SI, Kvetnoy IM · Bulletin of experimental biology and medicine 2012

Pancragen increased differentiation-marker expression in pancreatic cells, Bronchogen in bronchial cells, and Vesugen in prostatic fibroblasts. Responses were more pronounced in aged cultures.

Results and tables

Reported findings and study design

Pancragen increased differentiation-marker expression in pancreatic cells, Bronchogen in bronchial cells, and Vesugen in prostatic fibroblasts. Responses were more pronounced in aged cultures.

Human embryonic pancreatic and bronchial cell cultures, plus human prostatic fibroblasts, compared at different passage ages.

Results · Primary-publication indexed abstract
MeasureResultComparison, timing and statistics
Differentiation markersCXCL12/Hoxa3 or CXCL12/WEGC1 expression increased in the corresponding cultures
Preparation assignmentsPancragen KEDW → pancreas; Bronchogen AEDL → bronchial cells; Vesugen KED → prostatic fibroblasts

Different peptides were tested in different cell types; this is not a combination trial or evidence of organ recovery in patients. No numerical effect sizes are supplied.

Source for these results ↗ · Reviewed 2026-11-01

Population / setting
Human embryonic pancreatic and bronchial cell cultures, plus human prostatic fibroblasts, compared at different passage ages.
Source reviewed
Original-publication metadata and indexed abstract checked in Europe PMC. No unavailable full-text figures inferred.
Study limitations
  • Different peptides were tested in different cell types; this is not a combination trial or evidence of organ recovery in patients. No numerical effect sizes are supplied.

Reviewed 2026-11-01.

Read the source ↗
2026 · Peptidergic regulation of age-related alterations in the cardiovascular systemPreparations reviewed: Vascular polypeptide preparation, KED and AEDR
2026ReviewEnglish abstract

Peptidergic regulation of age-related alterations in the cardiovascular system

· Journal publication

Ryzhak GA, Popovich IG, Kozina LS, Arutionov VA, Arutjunyan AV · Advances in gerontology = Uspekhi gerontologii 39(4)

The review brings together vascular polypeptide, KED and AEDR research. It describes changes in endothelial endothelin-1 expression, vascular hemodynamics and experimental myocardial injury. These preparation-specific observations are preclinical; the review supplies no new human cardiovascular efficacy trial.

Results and tables

Reported findings and study design

The review brings together vascular polypeptide, KED and AEDR research. It describes changes in endothelial endothelin-1 expression, vascular hemodynamics and experimental myocardial injury. These preparation-specific observations are preclinical; the review supplies no new human cardiovascular efficacy trial.

Results · Indexed abstract checked
MeasureResultComparison, timing and statistics
Preparations reviewedVascular polypeptide preparation, KED and AEDR
Endothelial findingsKED restored elevated ET-1 expression toward normal in reported culturesCultures derived from patients are not a clinical treatment trial
Cardiac findingsAEDR experimental cardioprotection summarizedAnimal experiments; no new human trial

Review of earlier experiments, not independent replication. Vascular extracts, KED and AEDR are different preparations; effects cannot be transferred between them. Exact publication day is not supplied by the index; newly indexed 28 October 2026.

Source for these results ↗ · Reviewed 2026-10-31

Population / setting
Review of vascular-polypeptide, KED and AEDR experiments in endothelial cultures and animal cardiovascular models.
Source reviewed
Primary publication metadata and indexed abstract checked through Europe PMC on 31 October 2026. No unavailable effect sizes inferred.
Study limitations
  • Review of earlier experiments, not independent replication. Vascular extracts, KED and AEDR are different preparations; effects cannot be transferred between them. Exact publication day is not supplied by the index; newly indexed 28 October 2026.

Reviewed 2026-10-31.

Read the source ↗
2015 · [EFFECT OF SYNTHETIC PEPTIDES ON AGING OF PATIENTS WITH CHRONIC POLYMORBIDITY AND ORGANIC BRAIN SYNDROME OF THE CENTRAL NERVOUS SYSTEM IN REMISSION].Biological-age indicators: Authors reported favorable changes after Pinealon or Vesugen; comparative effect size unavailable
2015Uncontrolled human reportEnglish abstract

[EFFECT OF SYNTHETIC PEPTIDES ON AGING OF PATIENTS WITH CHRONIC POLYMORBIDITY AND ORGANIC BRAIN SYNDROME OF THE CENTRAL NERVOUS SYSTEM IN REMISSION].

Meshchaninov VN, Tkachenko EL, Zharkov SV, Gavrilov IV, Katyreva IuE · Advances in gerontology = Uspekhi gerontologii; 2015

The authors reported changes in biological-age indicators after Pinealon and Vesugen. They also reported prooxidant activity and lower circulating CD34-positive cell markers.

Results and tables

Reported findings and study design

Adults aged 41–83 with multiple conditions and organic brain syndrome in remission; Pinealon and Vesugen studied.

Results · Primary indexed abstract, PMID 26390612.
MeasureResultComparison, timing and statistics
Biological-age indicatorsAuthors reported favorable changes after Pinealon or Vesugen; comparative effect size unavailable
Oxidation and blood-cell markersProoxidant activity and lower circulating CD34-positive markers also reported
Printed total enrollment32
Printed sex breakdown18 men + 12 women = 30; does not reconcile with printed total

The abstract says 32 participants while listing 18 men and 12 women. It does not isolate preparation-specific effects or establish longevity, genetic safety or clinical harm.

Source for these results ↗ · Reviewed 2026-11-05

Population / setting
Adults aged 41–83 with multiple conditions and organic brain syndrome in remission
Source reviewed
Primary indexed abstract rechecked 5 November 2026. Both Pinealon and Vesugen are explicitly named; full paper and the 32-versus-30 participant discrepancy remain unresolved.
Study limitations
  • The abstract states 32 participants but lists 18 men and 12 women; the reported participant totals differ.
  • Allocation, comparator details and preparation-specific effects require the full paper.
  • The biomarker findings do not establish clinical harm, longevity benefit or genetic safety; favorable author conclusions should not erase the adverse-direction signals.

Reviewed 2026-11-05.

Read the source ↗
2008 · Investigation of antihypoxic properties of short peptides
2008Animal / experimentalEnglish abstract

Investigation of antihypoxic properties of short peptides

Synthetic peptide / defined-sequence research · Journal publication

Kozina LS · Advances in gerontology = Uspekhi gerontologii 21(1):61-67. PMID 18546825

The comparative report describes antihypoxic activity, with the largest effect for Pinealon in the tested model.

Population / setting
Experimental hypobaric/prenatal hypoxia models
Source reviewed
Europe PMC indexed citation and abstract checked. Full original paper not reviewed.
Study limitations
  • Model-specific ranking cannot be transferred to humans or occupational exposure protection.
  • Full methods, adverse-event reporting and independent replication remain to be appraised.

Reviewed 2026-09-30.

Read the source ↗
2008 · Biological activity of regulatory peptides in model experiments in vitro
2008In vitroEnglish abstract

Biological activity of regulatory peptides in model experiments in vitro

Synthetic peptide / defined-sequence research · Journal publication

Kozina LS, Arutiunian AV, Stvolinskiĭ SL, Khavinson VKh · Advances in gerontology = Uspekhi gerontologii 21(1):68-73. PMID 18546826

The peptides did not behave as direct antioxidants. Effects on lipid peroxidation, membrane stability and neuronal survival differed by peptide.

Population / setting
Lipoprotein, erythrocyte and neuronal model experiments
Source reviewed
Europe PMC indexed citation and abstract checked. Full original paper not reviewed.
Study limitations
  • Do not recast these model findings as a universal antioxidant or anti-aging effect.
  • Full methods, adverse-event reporting and independent replication remain to be appraised.

Reviewed 2026-09-30.

Read the source ↗
2014 · The efficacy of peptide bioregulators of vessels in lower limbs chronic arterial insufficiency treatment in old and elderly peopleBlood-flow and clinical measures: Improvement reported
2014Uncontrolled human reportEnglish abstract

The efficacy of peptide bioregulators of vessels in lower limbs chronic arterial insufficiency treatment in old and elderly people

Synthetic peptide / defined-sequence research · Journal publication

Kitachev KV, Sazonov AB, Kozlov KL, Petrov KIu, Sliusarev AS, Khavinson VKh · Advances in gerontology = Uspekhi gerontologii 27(1):156-159. PMID 25051774

Indexed title refers to lower-limb arterial insufficiency, but the abstract describes penile blood-flow measurements before and after Vezugen monotherapy. The mismatch is preserved pending original-paper review.

Results and tables

Reported findings and study design

41 patients with vasculogenic erectile dysfunction treated with Vesugen; clinical and penile-artery measurements before/after.

Results · Previously retrieved indexed abstract; numerical statements checked against the saved source text
MeasureResultComparison, timing and statistics
Blood-flow and clinical measuresImprovement reportedNo numerical flow-velocity or clinical-score difference provided

The abstract’s 80–90% figure concerns atherosclerosis background, not a Vesugen response rate; it is not used as an efficacy number.

Source for these results ↗ · Reviewed 2026-10-29

Population / setting
Abstract: 41 patients with vasculogenic erectile dysfunction
Source reviewed
Europe PMC indexed citation and abstract checked. Full original paper not reviewed.
Study limitations
  • Both descriptions refer to one 41-patient cohort. A separate postoperative lower-limb cohort requires its own original citation; no comparator is described in this abstract.
  • Full methods, adverse-event reporting and independent replication remain to be appraised.

Reviewed 2026-09-30.

Read the source ↗
· Vesugen — originating-institute clinical report
Year unconfirmedHuman comparative studyFull text available

Vesugen — originating-institute clinical report

Marketed product / formulation not independently verified · Institute report / commercial reproduction

Originating institute; report reproduced in commercial collection · Reports on clinical studies of CYTOMAX and CYTOGEN products; PDF page 101

Human report located; design quality and independent confirmation remain unresolved.

Population / setting
40 atherosclerosis patients: 25 adjunctive product, 15 conventional-care controls
Source reviewed
Relevant report text checked in the 125-page PDF edition; not the reported unlocated 152-page edition.
Study limitations
  • Commercially distributed institute report; independent peer review, randomization and blinding not established.
  • Product composition is not independently characterized here; do not equate a marketed formulation with a purified experimental sequence.
  • Reported absence of harms does not establish safety.

Reviewed 2026-09-30.

Read the source ↗
2016 · Peptide Regulation of Skin Fibroblast Functions during Their Aging In Vitro
2016In vitroEnglish abstract

Peptide Regulation of Skin Fibroblast Functions during Their Aging In Vitro

Lin'kova NS, Drobintseva AO, Orlova OA, Kuznetsova EP, Polyakova VO, Kvetnoy IM, Khavinson VKh · Bull Exp Biol Med 161(1):175-178. PMID 27259496

The peptides altered proliferation, remodeling and aging-associated protein markers. AED and AEDG also reduced caspase-dependent apoptosis in this model.

Population / setting
Aging skin-fibroblast cultures; KE, KED, AED and AEDG
Source reviewed
Indexed abstract and citation checked via Europe PMC / PubMed; full methods and risk of bias not appraised.
Study limitations
  • Cultured skin cells, not a human cartilage or longevity trial.
  • Changes in Ki-67, CD98hc, MMP-9 and caspase-3 do not establish tissue repair in patients.

Reviewed 2026-09-29.

Read the source ↗
2020 · Gene expression in human mesenchymal stem cell aging cultures: modulation by short peptides
2020In vitroEnglish abstract

Gene expression in human mesenchymal stem cell aging cultures: modulation by short peptides

Ashapkin V, Khavinson V, Shilovsky G, Linkova N, Vanuyshin B · Mol Biol Rep 47(6):4323-4329. PMID 32399807

AED, KED and KE changed expression of selected aging-related genes. Effects depended on peptide and culture-aging model; KED affected TNKS2 in opposite directions across models.

Population / setting
Human embryonic bone-marrow MSC line FetMSCs, aged in culture
Source reviewed
Indexed abstract and citation checked via Europe PMC / PubMed; full methods and risk of bias not appraised.
Study limitations
  • Human-derived cells are not human clinical participants.
  • Gene-expression changes do not establish improved cartilage repair, slower aging or safety.

Reviewed 2026-09-29.

Read the source ↗
2023 · Senescence-Associated Secretory Phenotype of Cardiovascular System Cells and Inflammaging: Perspectives of Peptide Regulation
2023ReviewFull text available

Senescence-Associated Secretory Phenotype of Cardiovascular System Cells and Inflammaging: Perspectives of Peptide Regulation

Khavinson V, Linkova N, Dyatlova A, Kantemirova R, Kozlov K · Cells 12(1):106 (2023 issue; online December 2022). DOI 10.3390/cells12010106

Discusses KED and AEDR. The reported AEDR rat-infarction benefit cites US patent 7,662,789 as reference 123; it is not presented here as a newly recovered peer-reviewed animal trial.

Population / setting
Cardiovascular senescence, cell models and animal research
Source reviewed
Full-text XML checked, including AEDR discussion and patent reference 123.
Study limitations
  • Claims about AEDR detection in heart complex are review-reported; original analytical evidence remains a recovery target.
  • Patent examples and experimental biomarkers do not establish clinical cardiovascular protection.

Reviewed 2026-09-29.

Read the source ↗
2019 · Effect of short peptides on neuronal differentiation of stem cells
2019In vitroEnglish abstract

Effect of short peptides on neuronal differentiation of stem cells

Caputi S, Trubiani O, Sinjari B, Trofimova S, Diomede F, Linkova N, Diatlova A, Khavinson V · Int J Immunopathol Pharmacol 33:2058738419828613. PMID 30791821

Examined AED, KED, KE, AEDG and their mixture. Increased neuronal-marker expression was reported for KED and the mixture.

Population / setting
Human periodontal-ligament stem-cell cultures
Source reviewed
Indexed abstract and citation checked via Europe PMC / PubMed; full methods and risk of bias not appraised.
Study limitations
  • Mixture results cannot be assigned to AED alone.
  • Marker expression is not proof of functional neuronal repair or a human clinical benefit.

Reviewed 2026-09-29.

Read the source ↗
2020 · Identification of short peptides in the composition of polypeptide complexes isolated from animal organs
2020Analytical / composition studyRussian source · see review scope

Identification of short peptides in the composition of polypeptide complexes isolated from animal organs

I. K. Zhurkovich, N. G. Kovrov, G. A. Ryzhak, E. S. Mironova, V. Kh. Khavinson · Uspekhi Sovremennoi Biologii 140(2):140–148

Reports KED in vessel complex, AED in cartilage, EDG and AEDL in bronchial mucosa, EDR in brain and KEDW in pancreas. This strengthens sequence-level links in the research program.

Population / setting
Animal-organ polypeptide complexes analyzed by UHPLC–MS
Source reviewed
Author-hosted Russian PDF: citation and indexed abstract checked; full analytical validation and product-batch equivalence not appraised.
Study limitations
  • Molecular detection does not prove identical pharmacology or clinical equivalence.
  • The paper’s discussion of clinical work is not an independent clinical trial.

Reviewed 2026-09-29.

Read the source ↗
2013 · Mechanism of Biological Activity of Short Peptides: Cell Penetration and Epigenetic Regulation of Gene Expression
2013ReviewFull text available

Mechanism of Biological Activity of Short Peptides: Cell Penetration and Epigenetic Regulation of Gene Expression

V. Kh. Khavinson, A. Yu. Solovyev, S. I. Tarnovskaya, N. S. Linkova · Biology Bulletin Reviews 3(6):451–455

Mechanistic review with a table of 15 short peptides on page 453. Tissue labels in the research map are the authors’ proposed targets, not established clinical indications.

Population / setting
Review of earlier research
Source reviewed
Author-hosted English PDF and its peptide table checked. Each cited experiment remains a separate appraisal task.
Study limitations
  • Source-linked does not mean a completed risk-of-bias review.
  • A review is not an independent clinical replication; proposed mechanisms do not establish efficacy or safety.

Reviewed 2026-09-27.

Read the source ↗
2012 · The peptide correction of neurotic disorders among professional truck-driversSociodemographic associations: Not statistically significant
2012Human comparative studyEnglish abstract

The peptide correction of neurotic disorders among professional truck-drivers

Pinealon and Vezugen peptide bioregulators, including combined use. The abstract does not specify the dosage form.

A. S. Bashkireva, V. G. Artamonova · Adv Gerontol. 25(4):718–728

The abstract describes occupational psychoemotional differences and reports changes with peptide bioregulators, including combined Pinealon and Vezugen.

Results and tables

Reported findings and study design

150 male lorry drivers (43.3 ± 0.9 years) and 150 male metal craftsmen (42.8 ± 0.9 years); three psychological-adaptation categories.

Protocol information

The indexed abstract names Pinealon and Vezugen, including combined use, but gives no dose, route or treatment duration. The separate locomotive-worker capsule regimen is not a verified protocol for these truck drivers.

Protocol source ↗ · Indexed publication abstract; original methods not retrieved

Results · Previously retrieved indexed abstract; numerical statements checked against the saved source text
MeasureResultComparison, timing and statistics
Sociodemographic associationsNot statistically significantp>0.1
Peptide-associated psychoemotional/adaptation changesStatistically significant range reportedp<0.001–0.05
Preferred combination in the authors’ reportPinealon + VesugenSeparate treatment-arm sizes and absolute outcome changes not stated

The 300-person occupational comparison is not a verified randomized-treatment denominator.

Source for these results ↗ · Reviewed 2026-10-29

Population / setting
150 male lorry drivers and 150 male metal craftsmen in the occupational comparison
Source reviewed
PubMed record and English abstract checked; intervention allocation and full methods not reviewed.
Study limitations
  • The occupational cohort size is not a verified randomized-treatment sample size.
  • Randomization, blinding, and intervention-group sizes are not established from the abstract.
  • Combination findings do not identify either peptide’s independent contribution or demonstrate fewer driving accidents.

Reviewed 2026-09-27.

Read the source ↗

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Research collection curated by @PepMariner · editorial standards. Send a source correction ↗

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