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COMPOUND RECORD / STEMOKIN

Stemokin / Neogen

Source linked
Research profile — evidence review incomplete. Topic tags are research navigation, not indications or recommendations. Source access does not establish effectiveness or safety.
01 / OVERVIEW

What is it?

Synthetic Ile–Glu–Trp tripeptide (IEW), studied in hematopoietic experiments and Russian clinical immune research. It is distinct from whole tissue extracts.

Research context

Synthetic Ile–Glu–Trp tripeptide (IEW), studied in hematopoietic experiments and Russian clinical immune research. It is distinct from whole tissue extracts.

Working classification
Peptide / preparation research
Research collection
Peptide bioregulation · editorial grouping
Institutional provenance
Not established for this compound record
Last evidence review
Full evidence review pending; source-check scope appears with each publication below.
02 / EVIDENCE DIMENSIONS

What do we know?

Human research
—Comparative clinical report; methods and overlap unresolved
Study methods
—Source-specific designs and limitations below
Independent replication
—Related reports are not automatically independent evidence
Source access
—Linked publications; access and review scope shown per record
Safety evidence
—Clinical safety, product equivalence and interactions not established by this collection

These are independent review fields, not a rating. Missing evidence in this starter does not mean no research exists.

Explore the expanded peptide research collection and unresolved source trails ↗

03 / SOURCE TRAIL

Linked sources

Explore the research map and unresolved leads ↗

2016Animal / experimentalEnglish abstract

Chemical Platform for the Preparation of Synthetic Orally Active Peptidomimetics with Hemoregulating Activity.

Preparation-specific research; no equivalence inferred

Deigin V, Ksenofontova O, Khrushchev A, Yatskin O, Goryacheva A, Ivanov V. · ChemMedChem

Five cyclic analogues, numbered 3–7, were synthesized; three showed activity in experimental hematopoietic assays. Normal-marrow stimulation and post-irradiation recovery differ. Oral activity is not a pharmacokinetic measurement.

Population / setting
See original report; human, animal and laboratory components must be distinguished.
What was checked
Indexed metadata and abstract checked via Europe PMC. Original full methods not reviewed.
Limitations & review scope
  • Full methods, preparation identity and risk of bias require appraisal.
  • Related publications may share experiments; source count is not independent-study count.

Source checked 2026-10-02. This is a source-linked record, not a completed evidence review.

Read the source ↗
2003Animal / experimentalEnglish abstract

[Immunogenic peptide neogen stimulates postradiation recovery thrombopoiesis].

Preparation-specific research; no equivalence inferred

Ziablitskiĭ VM, Semina OV, Semenets TN, Starosel'skaia AN, Romanovskaia VN, Mikhal'skaia TIu, Poverennyĭ AM, Deĭgin VI. · Radiatsionnaia biologiia, radioecologiia

Neogen was investigated for platelet and bleeding-time recovery after irradiation in mice. Animal recovery endpoints do not establish clinical hematologic benefit.

Population / setting
See original report; human, animal and laboratory components must be distinguished.
What was checked
Indexed metadata and abstract checked via Europe PMC. Original full methods not reviewed.
Limitations & review scope
  • Full methods, preparation identity and risk of bias require appraisal.
  • Related publications may share experiments; source count is not independent-study count.

Source checked 2026-10-02. This is a source-linked record, not a completed evidence review.

Read the source ↗
2024Animal / experimentalFull text available

Novel Peptidomimetic Cyclo-{E(I)-E(W)}Na (CP-88) with Hematopoietic Activity Sustained in Invasive and Oral Administration: Experimental and Preclinical Evaluation

Defined synthetic peptide / analogue

Vladislav Deigin, Yulia Vinogradova, Dmitriy Vinogradov, Natalia Linkova, Anastasiia Dyatlova, Dmitrii Medvedev, Alexander Krasichkov, Victoria Polyakova · International Journal of Molecular Sciences 25(24):13385

Mouse and laboratory experiments report colony-forming activity, CD34-positive-cell changes and NF-κB reporter activation. These do not establish long-term stem-cell self-renewal, direct Toll-like-receptor binding or a causal NF-κB mechanism. Oral experimental activity does not establish human pharmacokinetics; preclinical safety extrapolations are not safe human doses.

Population / setting
Source-specific experimental population
What was checked
Original full text retrieved from Europe PMC; experimental scope and interpretation checked. Supplementary methods and independent replication remain review targets.
Limitations & review scope
  • Independent replication and full risk-of-bias appraisal remain unresolved.
  • No personalized treatment or safety conclusion follows from this record.

Source checked 2026-10-02. This is a source-linked record, not a completed evidence review.

Read the source ↗
2023ReviewFull text available

Advancement from Small Peptide Pharmaceuticals to Orally Active Piperazine-2,5-dion-Based Cyclopeptides

Defined synthetic peptide / analogue

Vladislav Deigin, Natalia Linkova, Olga Volpina · International Journal of Molecular Sciences 24(17):13534

Development-group review connecting small peptides with cyclic peptidomimetics, including AWE18. AWE18 and CP-88 are separate candidates. Review descriptions of oral activity are not independent clinical trials.

Population / setting
Source-specific experimental population
What was checked
Review full text retrieved via Europe PMC. Primary compound-specific studies require separate appraisal.
Limitations & review scope
  • Independent replication and full risk-of-bias appraisal remain unresolved.
  • No personalized treatment or safety conclusion follows from this record.

Source checked 2026-10-02. This is a source-linked record, not a completed evidence review.

Read the source ↗
2015Human comparative studyRussian source · see review scope

Stemokin in treatment and prevention of pyoderma in military personnel

Defined synthetic peptide / analogue

V. V. Gladko, N. N. Kakhishvili, S. A. Masyukova · See linked publication

The report compares adjunctive treatment in groups of 39 and 37, and prevention in groups of 40 and 36. Reported recovery was 74.36% versus 21.62%; reported infection incidence was 17.5% versus 58.3% during follow-up up to 12 months. Allocation and blinding are unclear. The 2011 dissertation appears to report overlapping groups; neither publications nor the two investigations establish 152 unique participants.

Population / setting
Source-specific experimental population
What was checked
Russian conference abstract read. Full dissertation and participant-overlap audit remain pending.
Limitations & review scope
  • Independent replication and full risk-of-bias appraisal remain unresolved.
  • No personalized treatment or safety conclusion follows from this record.

Source checked 2026-10-02. This is a source-linked record, not a completed evidence review.

Read the source ↗
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