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RESEARCH FAMILY / NT3-MIMETICS

NT-3 mimetics: GTS-301 & GTS-302ГТС-301 / ГТС-302

CognitionStress
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?

A paired NT-3 research record comparing two loop-4 mimetics with different downstream signaling and animal pharmacology.

Research context

A paired NT-3 research record comparing two loop-4 mimetics with different downstream signaling and animal pharmacology.

What the studies found

animal · 2022

Cell cultures and mice

GTS-301 activated TrkC and TrkB, protected HT-22 cells in injury assays and showed antidepressant-like activity in a mouse forced-swim experiment.

Limit: Preclinical findings do not establish human benefit or safety.

The First Dipeptide Mimetic of Neurotrofin-3: Design and Pharmacological Properties. ↗

animal · 2024

Morphine-dependent rats and HT-22 cells

GTS-301 and GTS-302 reduced withdrawal signs in morphine-dependent rats; only GTS-302 reduced withdrawal-associated mechanical allodynia. Cell assays reported different downstream signaling, with AKT/mTOR recruitment for GTS-302. A 2025 erratum is linked separately; quantitative estimates are withheld pending reconciliation.

Limit: Animal withdrawal models are not evidence for treating opioid dependence in people.

Low-Molecular Neurotrophin-3 Mimetics with Different Patterns of Postreceptor Signaling Activation Attenuate Differentially Morphine Withdrawal in Rats. ↗

animal · 2025

Mice and rats

GTS-302 altered forced-swim, elevated-plus-maze and object-recognition outcomes in rodents, without changing hot-plate pain sensitivity in the reported tests.

Limit: Preclinical findings do not establish human benefit or safety.

Study of the Pharmacological Activity Spectrum of the New Original NT-3 Mimetic Dipeptide GTS-302. ↗

Selected findings, not a systematic review or a treatment recommendation. Combination and related-preparation results cannot be attributed to this compound alone. See each source for access status and remaining limitations.

Working classification
Peptide research family
Research collection
Neuropeptide research · 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
—No human treatment trial assessed for this family
Study methods
—Member-specific studies; patents and archival leads identified separately
Independent replication
—Independent replication not established by the records collected here
Source access
—Primary abstracts, selected full texts, patents and explicit retrieval targets
Safety evidence
—Cell and animal effects do not establish human safety; analogues may differ

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

IDENTITY / MEMBER-SPECIFIC EVIDENCE

Inside this research family

Grouping supports navigation. It does not imply equivalent composition, mechanisms, effectiveness or safety.

Research objects, findings and source boundaries
MemberIdentityWhat the source supports
GTS-301Dimeric succinyl-Asn-Asn mimetic

Cell protection and mouse behavioral findings; later rat analgesia experiments are separate outcomes.

The First Dipeptide Mimetic of Neurotrofin-3: Design and Pharmacological Properties. ↗

Analgesic Activity of the Low Molecular Weight Neurotrophin-3 Dipeptide Mimetic GTS-301. ↗

GTS-302Dimeric hydroxybutyryl-Glu-Asn mimetic

Rodent anxiety-, memory- and antidepressant-like tests; no hot-plate effect reported.

Study of the Pharmacological Activity Spectrum of the New Original NT-3 Mimetic Dipeptide GTS-302. ↗

Direct comparisonTrkC/TrkB-related signaling

Different withdrawal and mechanical-pain responses; the 2025 correction must be reconciled.

Low-Molecular Neurotrophin-3 Mimetics with Different Patterns of Postreceptor Signaling Activation Attenuate Differentially Morphine Withdrawal in Rats. ↗

Erratum to: Low-Molecular Neurotrophin-3 Mimetics with Different Patterns of Postreceptor Signaling Activation Attenuate Differentially Morphine Withdrawal in Rats. ↗

Interpretation and open questions

The withdrawal paper reports ERK/PLCγ signaling for GTS-301 and additional AKT/mTOR activation for GTS-302. These are experimental profiles, not treatment-selection rules.

The patent and subsequent papers may describe overlapping experiments. A 2026 stroke-comparison citation remains an acquisition target until the original report is checked.

Explore the Russian peptide research map ↗

03 / SOURCE TRAIL

Linked sources

Explore the research map and unresolved leads ↗

2022Animal / experimentalEnglish abstract

The First Dipeptide Mimetic of Neurotrofin-3: Design and Pharmacological Properties.

Gudasheva TA, Sazonova NM, Tarasiuk AV, Logvinov IO, Antipova TA, Nikiforov DM, Povarnina PY, Seredenin SB · Doklady. Biochemistry and biophysics

GTS-301 activated TrkC and TrkB, protected HT-22 cells in injury assays and showed antidepressant-like activity in a mouse forced-swim experiment.

Population / setting
Cell cultures and mice
What was checked
Primary publication metadata and indexed abstract checked via Europe PMC; full methodological review pending.
Limitations & review scope
  • Preclinical findings do not establish human benefit or safety.
  • Indexed abstract reviewed; full methods and independent replication require appraisal.

Source checked 2026-10-05. This is a source-linked record, not a completed evidence review.

Read the source ↗
2024Animal / experimentalEnglish abstract

Low-Molecular Neurotrophin-3 Mimetics with Different Patterns of Postreceptor Signaling Activation Attenuate Differentially Morphine Withdrawal in Rats.

Kolik LG, Konstantinipolsky MA, Nikolaev SV, Logvinov IO, Antipova TA, Gudasheva TA · Biochemistry. Biokhimiia

GTS-301 and GTS-302 reduced withdrawal signs in morphine-dependent rats; only GTS-302 reduced withdrawal-associated mechanical allodynia. Cell assays reported different downstream signaling, with AKT/mTOR recruitment for GTS-302. A 2025 erratum is linked separately; quantitative estimates are withheld pending reconciliation.

Population / setting
Morphine-dependent rats and HT-22 cells
What was checked
Primary publication metadata and indexed abstract checked via Europe PMC; full methodological review pending.
Limitations & review scope
  • Animal withdrawal models are not evidence for treating opioid dependence in people.
  • Erratum PMID 40254407 must be reconciled with the full article before relying on numerical estimates.

Source checked 2026-10-05. This is a source-linked record, not a completed evidence review.

Read the source ↗
2025Not classifiedBibliographic record

Erratum to: Low-Molecular Neurotrophin-3 Mimetics with Different Patterns of Postreceptor Signaling Activation Attenuate Differentially Morphine Withdrawal in Rats.

Kolik LG, Konstantinipolsky MA, Nikolaev SV, Logvinov IO, Antipova TA, Gudasheva TA · Biochemistry. Biokhimiia

Published correction to the 2024 GTS-301/GTS-302 withdrawal paper. The correction text has not been recovered; this is not another experiment.

Population / setting
Correction notice
What was checked
Correction metadata and link to original publication checked.
Limitations & review scope
  • No abstract available; content of the correction remains to be reviewed.
  • Not an independent study or replication.

Source checked 2026-10-05. This is a source-linked record, not a completed evidence review.

Read the source ↗
2025Animal / experimentalEnglish abstract

Study of the Pharmacological Activity Spectrum of the New Original NT-3 Mimetic Dipeptide GTS-302.

Nikiforov DM, Povarnina PY, Gudasheva TA, Nadorova AV, Kolik LG, Valdman EA, Vakhitova YV, Seredenin SB · Doklady. Biochemistry and biophysics

GTS-302 altered forced-swim, elevated-plus-maze and object-recognition outcomes in rodents, without changing hot-plate pain sensitivity in the reported tests.

Population / setting
Mice and rats
What was checked
Primary publication metadata and indexed abstract checked via Europe PMC; full methodological review pending.
Limitations & review scope
  • Preclinical findings do not establish human benefit or safety.
  • Indexed abstract reviewed; full methods and independent replication require appraisal.

Source checked 2026-10-05. This is a source-linked record, not a completed evidence review.

Read the source ↗
2025Animal / experimentalEnglish abstract

Analgesic Activity of the Low Molecular Weight Neurotrophin-3 Dipeptide Mimetic GTS-301.

Kolik LG, Konstantinopolsky MA, Sazonova NM, Durnev AD, Gudasheva TA · Doklady. Biochemistry and biophysics

GTS-301 increased rat tail-flick pain thresholds by about 20–30%, with a reported effect lasting at least 24 hours in this experiment. This endpoint is distinct from the GTS-302 hot-plate test.

Population / setting
Rats; acute experimental pain testing
What was checked
Primary publication metadata and indexed abstract checked via Europe PMC; full methodological review pending.
Limitations & review scope
  • Preclinical findings do not establish human benefit or safety.
  • Indexed abstract reviewed; full methods and independent replication require appraisal.

Source checked 2026-10-05. This is a source-linked record, not a completed evidence review.

Read the source ↗
2023Patent / reported experimentsRussian source · see review scope

Dimeric dipeptide mimetics of neurotrophin-3 — RU2800369C9

· Primary source linked above

The patent describes the NT-3 mimetic series underlying GTS-301 and GTS-302. Patent examples may overlap with later publications and are not independent clinical evidence.

Population / setting
Patent chemistry and preclinical examples
What was checked
Selected original-source text checked; full methodological review pending.
Limitations & review scope
  • Patent claims are not evidence of approved clinical uses.
  • Reconcile shared experiments and corrected publication records.

Source checked 2026-10-05. This is a source-linked record, not a completed evidence review.

Read the source ↗
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