Histrelin

Histrelin

SCHEMBL18715

CC(=O)O.CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1cn(Cc2ccccc2)cn1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H]1CCC(=O)N1

nearest known ligand 0.78

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GNRHR

The experimentally established mechanism targets of Histrelin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
GNRHR known ✓ P30968 2/20 0.76
ABCC2 Q92887 1/20 0.78
PTGS1 P23219 1/20 0.70
APLNR P35414 4/20 0.59
CXCR4 P61073 2/20 0.56
MC4R P32245 1/20 0.56
MC5R P33032 1/20 0.56
MC3R P41968 1/20 0.56
MC1R Q01726 1/20 0.56

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Histrelin SCHEMBL5327685 1.00 ABCC2 (0.78) ABCC2GNRHRPTGS1APLNRCXCR4
Histrelin SCHEMBL29372688 1.00 ABCC2 (0.78) ABCC2GNRHRPTGS1APLNRCXCR4
Histrelin SCHEMBL17881 0.99 GNRHR (0.77) ABCC2GNRHRPTGS1APLNRCXCR4
Histrelin SCHEMBL29405757 0.99 GNRHR (0.77) ABCC2GNRHRPTGS1APLNRCXCR4
Histrelin SCHEMBL7619565 0.99 GNRHR (0.77) ABCC2GNRHRPTGS1APLNRCXCR4
Histrelin SCHEMBL84261 0.99 GNRHR (0.76) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL570851 0.94 ABCC2 (0.87) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL3174 0.94 ABCC2 (0.87) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL177978 0.94 ABCC2 (0.87) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL847084 0.94 ABCC2 (0.87) ABCC2GNRHRPTGS1APLNRCXCR4

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Appears in 7530 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122056884-A Methods of treating pancreatic cancer 坎莫森特里克斯公司 2026-05-19 CN claimed
US-12509465-B2 Benzoimidazole derivatives as anticancer agents CENTRE LEON BERARD (FR) 2025-12-30 US claimed
EP-4643858-A1 METHODS AND PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF UTERINE DISEASE Institut National de la Santé et de la Recherche Médicale (FR) 2025-11-05 EP claimed
US-20250262270-A1 COMPOSITIONS AND METHODS FOR TREATING PRECOCIOUS PUBERTY ENDO OPERATIONS LIMITED (IE) 2025-08-21 US claimed
US-20250213523-A1 COMBINATION OF HDAC INHIBITORS AND STATINS FOR USE IN THE TREATMENT OF PANCREATIC CANCER ISTITUTO NAZIONALE TUMORI IRCCS - FONDAZIONE G. PASCALE (IT) 2025-07-03 US claimed
EP-4566675-A2 HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS Incyte Corporation (US) 2025-06-11 EP claimed
US-20250177358-A1 COMBINATION OF SMALL MOLECULE CD-47 INHIBITORS WITH OTHER ANTI-CANCER AGENTS AURIGENE DISCOVERY TECHNOLOGIES LIMITED (IN) 2025-06-05 US claimed
US-12268670-B2 Combination of small molecule CD-47 inhibitors with other anti-cancer agents AURIGENE ONCOLOGY LIMITED (IN) 2025-04-08 US claimed
CN-119546293-A Combination of HDAC inhibitors and statins for the treatment of pancreatic cancer 国家癌症研究所IRCCS-G·帕斯卡莱基金会 2025-02-28 CN claimed
US-20250051384-A1 NEUTRAL GLYCOSYLATED AMIDES AND DIANIONIC GLUCURONIDATED ACIDS AS STABILIZERS FOR BIOLOGICAL MOLECULES EXTREMOCHEM, LDA. (PT) 2025-02-13 US claimed
US-20070281934-A1 INDOLE DERIVATIVES AS INHIBITORS OF HISTONE DEACETYLASE PHARMACYCLICS, INC. (US) 2007-12-06 US claimed
WO-2007109178-A2 INDOLE DERIVATIVES AS INHIBITORS OF HISTONE DEACETYLASE PHARMACYCLICS, INC. (US) 2007-09-27 WO claimed
EP-1773293-A2 COMPOSITIONS AND METHODS FOR TREATING CENTRAL PRECOCIOUS PUBERTY Valera Pharmaceuticals, Inc. (US) 2007-04-18 EP claimed
US-20060240092-A1 drug loaded micelle of a triblock polymer tert-butylphenylsilylpropene-polyethylene glycol-b-poly(tert-butylaspartic acid-b-polyphenylalanine-copoly( tert-buyltyrosine) has a drug-loaded inner core, a crosslinked outer core, and a hydrophilic shell INTEZYNE TECHNOLOGIES, INC. 2006-10-26 US claimed
WO-2006107903-A2 POLYMERIC MICELLES FOR DRUG DELIVERY INTEZYNE TECHNOLOGIES, INCORPORATED (US) 2006-10-12 WO claimed
WO-2006009801-A2 COMPOSITIONS AND METHODS FOR TREATING CENTRAL PRECOCIOUS PUBERTY VALERA PHARMACEUTICALS, INC. (US) 2006-01-26 WO claimed
US-20060019903-A1 Compositions and methods for treating precocious puberty COMPUTERSHARE TRUST COMPANY, NATIONAL ASSOCIATION 2006-01-26 US claimed
US-6096764-A ELIMINATING THE DETRIMENTAL SIDE-EFFECTS ASSOCIATED WITH THE CONTINUOUS AND CHRONIC USE OF GONDATROPIN-RELEASING HORMONE FACTOR OR AGONIST BY ADMINISTERING TO THE PATIENT AN EFFECTIVE AMOUNT OF BENZOTHIOPHENE DERIVATIVES ELI LILLY AND COMPANY (US) 2000-08-01 US claimed
WO-1999008677-A1 METHODS FOR INHIBITING DETRIMENTAL SIDE-EFFECTS DUE TO GnRH OR GnRH AGONIST ADMINISTRATION ELI LILLY AND COMPANY (US) 1999-02-25 WO claimed
EP-0897721-A2 Benzo(b)thiophene derivatives for inhibiting detrimental side-effects due to GnRH or GnRH agonist administration ELI LILLY AND COMPANY (US) 1999-02-24 EP claimed