Home / Research library / PT-141
PT-141: molecular data, studies & sources
PT-141 is catalogued here as a research compound. This profile brings together the molecular source record, selected indexed publications and available supplier comparisons. Evidence for a named substance does not authenticate a commercial product.
Compiled by PeptideTech Editors · Sources checked · Selected bibliography, not a systematic review
Molecular formula, weight & structure
- Molecular formula (MF)
- C50H68N14O10
- Molecular weight (MW)
- 1025.2 g/mol
- PubChem compound ID
- 9941379
- Record title
- Bremelanotide
Values describe the selected PubChem molecular entity. Counterions, salt forms, hydration and sequence changes can alter the supplied material. Confirm the exact identity against the supplier specification.
Source: PubChem CID 9941379 · retrieved 2026-09-21

Chemical identifiers and source data
- IUPAC name
- (3S,6S,9R,12S,15S,23S)-15-[[(2S)-2-acetamidohexanoyl]amino]-9-benzyl-6-[3-(diaminomethylideneamino)propyl]-12-(1H-imidazol-5-ylmethyl)-3-(1H-indol-3-ylmethyl)-2,5,8,11,14,17-hexaoxo-1,4,7,10,13,18-hexazacyclotricosane-23-carboxylic acid
- InChIKey
- FFHBJDQSGDNCIV-MFVUMRCOSA-N
- SMILES
- CCCC[C@@H](C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](NC(=O)[C@@H](NC1=O)CC2=CN=CN2)CC3=CC=CC=C3)CCCN=C(N)N)CC4=CNC5=CC=CC=C54)C(=O)O)NC(=O)C
Identifiers & sequence
- PubChem CID
- 9941379
- CAS Registry Number
- 189691-06-3via ChemIDplus, EPA DSSTox, FDA GSRS
- FDA UNII
- 6Y24O4F92S
- ChEMBL ID
- CHEMBL2070241
- InChIKey
- FFHBJDQSGDNCIV-MFVUMRCOSA-N
- Wikidata
- Q415353
Other names and development codes: PT-141 FREE BASE
Peptide sequence · 7 residues (one-letter code; X marks a residue without a one-letter code)
XDHFRWK
Condensed notation with terminal groups and non-standard residues
Ac-Nle-Asp(1)-His-D-Phe-Arg-Trp-Lys(1)-OH
Source: PubChem Biologic Line Notation. A reference sequence for the record, not an analysis of a supplied batch.
CAS numbers are published only from ChemIDplus, EPA DSSTox or the FDA Global Substance Registration System; UNII codes are confirmed in FDA GSRS by structure, sequence or exact name. Checked 2026-10-07.
Calculated molecular descriptors
| Monoisotopic (exact) mass | 1024.5243 Da |
|---|---|
| Heavy atoms | 74 |
| Hydrogen-bond donors | 13 |
| Hydrogen-bond acceptors | 11 |
| Rotatable bonds | 17 |
| Topological polar surface area | 379.0 Ų |
| Calculated logP (Crippen) | -0.65 |
| Rings | 5 |
| Stereocenters | 7 |
| Formal charge | 0 |
Computed with RDKit from the published SMILES (Crippen logP, topological polar surface area). Calculated descriptors are not measured properties of a supplied batch.
US regulatory status & drug development
PT-141 (bremelanotide; listed as bremelanotide acetate) is the active ingredient of VYLEESI, approved by the FDA under NDA 210557 (COSETTE) on June 21, 2019; Drugs@FDA lists it as a marketed prescription product (checked October 7, 2026). Research-labelled PT-141 listings are not VYLEESI and are not FDA-approved drugs.
| Medicine | Application | Sponsor | First approval | Marketing status |
|---|---|---|---|---|
| VYLEESIbremelanotide acetate | NDA 210557DailyMed label: Vyleesi · 2025-11-13 | COSETTE | Prescription |
An FDA approval covers a defined medicine, formulation and labelled use. It does not extend to research-labelled material sold under the same compound name. Identity basis: PT-141 is the development name of bremelanotide; the approved product lists bremelanotide acetate (research record PubChem CID 9941379).
Source: Drugs@FDA via openFDA (application records; DailyMed label set IDs) · checked . openFDA data are not intended for clinical decisions.
Drug development record (ChEMBL)
Harmonized drug-development record from ChEMBL. The highest clinical stage is the furthest stage reached, as recorded by ChEMBL; it can lag regulatory approvals, and it is not an approval of a research-supplier product.
- ChEMBL ID
- CHEMBL2070241
- Modality
- Protein / peptide
- Highest clinical stage
- Approved in at least one jurisdiction (ChEMBL phase 4)
- Record name
- BREMELANOTIDE
Mechanism of action
- Melanocortin receptor 4 agonist · target: Melanocortin receptor 4 (MC4R)
Synonyms, codes and trade names
- Trade and brand names (Drugs@FDA)
- VYLEESI · VYLEESI (AUTOINJECTOR)
- Synonyms and development codes
- Bremelanotide · PT-141 · PT-141 FREE BASE
Identity check: Identical standard InChIKey to the PubChem record. Source: ChEMBL CHEMBL2070241 (EMBL-EBI, CC BY-SA 3.0) · retrieved 2026-10-07
Registered clinical trials
Studies registered on ClinicalTrials.gov that list Bremelanotide as an intervention. Studies that only measure the molecule as a biomarker, or use it only as a comparator or background arm for another drug, are excluded. A registration describes a planned or completed protocol; it does not report a result. Active studies are listed first.
10 registered studies matched, 1 currently active or recruiting, 4 with results posted on ClinicalTrials.gov.
- By highest phase
- Phase 4 · 2Phase 3 · 3Phase 2 · 4Phase 1 · 1
- By registry status
- Completed · 9Active Not Recruiting · 1
| Study | Phase · status | Conditions | Sponsor · size |
|---|---|---|---|
| A Phase 2 Study Evaluating the Co-Administration of Bremelanotide With Tirzepatide for the Treatment of ObesityNCT06565611 · start 2024-08-05 · primary completion 2025-02-05 | Phase 2Active Not Recruiting | Obesity | Palatin Technologies, Inc108 participants |
| Single Dose of Vyleesi in Lactating Female Subjects to Measure the Concentration of Bremelanotide in Breast MilkNCT06867835 · start 2025-07-11 · primary completion 2025-11-15 | Phase 4Completed | Lactating Mother | Cosette Pharmaceuticals, Inc.10 participants |
| A Phase IIb, Multicenter, Open-Label, Prospective Study of Bremelanotide in Diabetic Kidney DiseaseNCT05709444 · start 2022-12-26 · primary completion 2024-04-26 | Phase 2Completed | Kidney Disease | Palatin Technologies, Inc16 participants |
| A Phase 3, Bridging, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Trial to Evaluate the Efficacy and Safety of Subcutaneously Administered Bremelanotide in Premenopausal Women With Hypoactive Sexual Desire Disorder (With or Without Decreased Arousal)NCT04943068 · start 2021-05-10 · primary completion 2023-05-16 | Phase 3Completed | Hypoactive Sexual Desire Disorder | Kwang Dong Pharmaceutical co., ltd.193 participants |
| Role of the Melanocortin-4 Receptor in Hypoactive Sexual Desire DisorderNCT04179734 · start 2019-10-07 · primary completion 2020-10-06 | Phase 4CompletedResults posted 2024-08-09 | Hypoactive Sexual Desire Disorder | Imperial College Healthcare NHS Trust40 participants |
| Study to Evaluate Rate of Nausea in Healthy Premenopausal Female Subjects Treated With Single Dose of Bremelanotide Alone or With ZofranNCT03973047 · start 2019-06-17 · primary completion 2019-07-19 | Phase 1Completed | Nausea | AMAG Pharmaceuticals, Inc.228 participants |
| 2. Study to Evaluate the Efficacy/Safety of Bremelanotide in Premenopausal Women With Hypoactive Sexual Desire DisorderNCT02338960 · start 2015-01 · primary completion 2016-08 | Phase 3CompletedResults posted 2021-01-28 | Hypoactive Sexual Desire Disorder | Palatin Technologies, Inc714 participants |
| 1. Study to Evaluate the Efficacy/Safety of Bremelanotide in Premenopausal Women With Hypoactive Sexual Desire DisorderNCT02333071 · start 2014-12 · primary completion 2016-07 | Phase 3CompletedResults posted 2020-12-23 | Hypoactive Sexual Desire Disorder | Palatin Technologies, Inc723 participants |
| Bremelanotide in Premenopausal Women With Female Sexual Arousal Disorder and/or Hypoactive Sexual Desire DisorderNCT01382719 · start 2011-06 · primary completion 2012-09 | Phase 2CompletedResults posted 2014-04-14 | Female Sexual Arousal Disorder · Hypoactive Sexual Desire Disorder | Palatin Technologies, Inc612 participants |
| Evaluate the Safety and Efficacy of Bremelanotide in Women With Female Sexual Arousal Disorder (FSAD)NCT00425256 · start 2006-02 · primary completion 2007-05 | Phase 2Completed | Sexual Arousal Disorder | Palatin Technologies, IncEnrollment not listed |
Registry check 2026-10-09 · Run this search on ClinicalTrials.gov
Human intervention studies
Selected studies in which participants received Bremelanotide, with their indexed or reviewed study type. Check the original article for the formulation, population and controls. Studies that only measured the molecule, or used it as a comparator, are listed separately below and are not counted as intervention studies.
- Human study · PubMed trial index Compound given to participants
Safety Profile of Bremelanotide Across the Clinical Development Program.
Clayton AH, Kingsberg SA, Portman D et al. · Journal of women's health (2002) · 2022
PMID 35147466 · DOI: 10.1089/jwh.2021.0191 · Registration NCT02333071, NCT02338960
- Human study · PubMed trial index Compound given to participants
Bremelanotide for the Treatment of Hypoactive Sexual Desire Disorder: Two Randomized Phase 3 Trials.
Kingsberg SA, Clayton AH, Portman D et al. · Obstetrics and gynecology · 2019
PMID 31599840 · DOI: 10.1097/AOG.0000000000003500 · Registration NCT02333071, NCT02338960
- Human study · PubMed trial index Compound given to participants
Prespecified and Integrated Subgroup Analyses from the RECONNECT Phase 3 Studies of Bremelanotide.
Simon JA, Kingsberg SA, Portman D et al. · Journal of women's health (2002) · 2022
PMID 35230162 · DOI: 10.1089/jwh.2021.0225
- Human study · PubMed trial index Compound given to participants
Salvage of sildenafil failures with bremelanotide: a randomized, double-blind, placebo controlled study.
Safarinejad MR, Hosseini SY · The Journal of urology · 2008
PMID 18206919 · DOI: 10.1016/j.juro.2007.10.063
- Human study · PubMed trial index Compound given to participants
Responder Analyses from a Phase 2b Dose-Ranging Study of Bremelanotide.
Althof S, Derogatis LR, Greenberg S et al. · The journal of sexual medicine · 2019
PMID 31277966 · DOI: 10.1016/j.jsxm.2019.05.012
- Human study · PubMed trial index Compound given to participants
Bremelanotide for female sexual dysfunctions in premenopausal women: a randomized, placebo-controlled dose-finding trial.
Clayton AH, Althof SE, Kingsberg S et al. · Women's health (London, England) · 2016
PMID 27181790 · DOI: 10.2217/whe-2016-0018 · Registration NCT01382719
Preclinical research, reviews & other publications
Animal studies, laboratory experiments, reviews and other indexed papers answer different questions. A review is secondary evidence; a case report does not estimate how often an outcome occurs.
- Review · secondary evidence
Bremelanotide: First Approval.
Dhillon S, Keam SJ · Drugs · 2019
PMID 31429064 · DOI: 10.1007/s40265-019-01187-w
PT-141 supplier sources
Scientific sources describe molecules and experiments. The commercial links below identify recorded supplier packages. A publication or chemical database entry does not verify the seller, purity, sterility or contents of a lot. Some links are affiliate links; see our disclosure.
PT-141 for sale: compare prices, sizes and forms from every tracked supplier →
| Supplier | Recorded packages | Example source listing |
|---|---|---|
| Blank PeptidesUSD | 10mg Vial1 recorded offers | 10mg Vial · $55.00Stale observation · Checked Sep 30, 2026Supplier listing, PT-141 10mg Vial, Blank Peptides, opens in a new tab |
| American PeptidesUSD | 10mg Vial · 10mg Spray2 recorded offers | 10mg Spray · $90.00Checked Nov 6, 2026Supplier listing, PT-141 10mg Spray, American Peptides, opens in a new tab |
| Amino ClubUSD | 10mg Vial · 15mg Spray2 recorded offers | 10mg Vial · $29.99Stale observation · Checked Oct 14, 2026Supplier listing, PT-141 10mg Vial, Amino Club, opens in a new tab |
| Nova Peptide SupplyUSD | 10mg Vial1 recorded offers | 10mg Vial · $39.99Checked Nov 6, 2026Supplier listing, PT-141 10mg Vial, Nova Peptide Supply, opens in a new tab |
| Amino USAUSD | 10mg Vial1 recorded offers | 10mg Vial · $45.00Checked Nov 6, 2026Supplier listing, PT-141 10mg Vial, Amino USA, opens in a new tab |
| Cenexa LabsUSD | 10mg Vial · 10mg Spray2 recorded offers | 10mg Vial · $44.99Checked Nov 6, 2026Supplier listing, PT-141 10mg Vial, Cenexa Labs, opens in a new tab |
| LA PeptidesUSD | 10mg Spray · 10mg Vial2 recorded offers | 10mg Spray · $59.99Checked Nov 3, 2026Supplier listing, PT-141 10mg Spray, LA Peptides, opens in a new tab |
Reference sources & further reading
- PubChem compound record 9941379 — chemical identity and structure.
- ChEMBL drug record CHEMBL2070241 — development stage, mechanism and synonyms.
- FDA Global Substance Registration System: UNII 6Y24O4F92S — substance identity, names and codes.
- Drugs@FDA: NDA 210557 — US approval record for a medicine with the same active ingredient.
- Wikipedia: Bremelanotide — Background encyclopedia; not a primary clinical source.
The citations above link directly to publication records. Encyclopedia links are background reading and are not used to establish clinical effectiveness.
Search for additional research
These links run searches; their results have not been individually reviewed and can include unrelated compounds.
Research information is not a dosing guide or a recommendation for personal use. Study findings are specific to the formulation, population and methods tested. Read our source and correction policy.
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