Leuprolide

Leuprolide

SCHEMBL713554

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](CC(C)C)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.Cl.Clc1cccc(C(c2ccc3[nH]cnc3c2)n2ccnc2)c1

nearest known ligand 0.69

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GNRHR

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

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
GNRHR known ✓ P30968 2/20 0.67
ABCC2 Q92887 1/20 0.69
PTGS1 P23219 1/20 0.62
APLNR P35414 4/20 0.55
CXCR4 P61073 2/20 0.52

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
Leuprolide SCHEMBL28264908 0.90 GNRHR (0.78) ABCC2GNRHRPTGS1APLNR
Leuprolide SCHEMBL570851 0.88 ABCC2 (0.87) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL847084 0.88 ABCC2 (0.87) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL3174 0.88 ABCC2 (0.87) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL177978 0.88 ABCC2 (0.87) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL3915060 0.88 GNRHR (0.86) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL7751433 0.87 GNRHR (0.86) ABCC2GNRHRPTGS1APLNRCXCR4
Deslorelin SCHEMBL1649660 0.87 GNRHR (0.86) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL21540132 0.87 GNRHR (0.86) ABCC2GNRHRPTGS1APLNRCXCR4
Leuprolide SCHEMBL10061885 0.87 GNRHR (0.86) 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

Claimed or disclosed in 88 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20060079472-A1 Methods for treating angiogenesis ANGIOSYN, INC. 2006-04-13 US claimed
CN-115461054-A Elongation factor 1-alpha inhibitor and application thereof 加利福尼亚大学董事会 2022-12-09 CN disclosed
CN-113543800-A DNA monoclonal antibodies targeting PD-1 for treatment and prevention of cancer 威斯塔解剖学和生物学研究所 2021-10-22 CN disclosed
EP-3381945-B1 HUMAN MONOCLONAL ANTIBODIES TO ACTIVIN RECEPTOR-LIKE KINASE-1 AMGEN FREMONT INC (US) 2020-08-19 EP disclosed
EP-3381945-A1 HUMAN MONOCLONAL ANTIBODIES TO ACTIVIN RECEPTOR-LIKE KINASE-1 Amgen Fremont Inc. (US) 2018-10-03 EP disclosed
EP-2960253-B1 HUMAN MONOCLONAL ANTIBODIES TO ACTIVIN RECEPTOR-LIKE KINASE-1 AMGEN FREMONT INC (US) 2018-06-06 EP disclosed
US-20160361337-A1 FORMULATIONS OF ACADESINE MERCK SHARP & DOHME CORP. (US) 2016-12-15 US disclosed
US-20160213737-A1 Methods and Compositions for Treating Conditions NEOPRO LABS, LLC 2016-07-28 US disclosed
EP-2960253-A1 HUMAN MONOCLONAL ANTIBODIES TO ACTIVIN RECEPTOR-LIKE KINASE-1 Amgen Fremont Inc. (US) 2015-12-30 EP disclosed
US-9221915-B2 Human monoclonal antibodies to activin receptor-like kinase-1 PFIZER INC. (US) 2015-12-29 US disclosed
US-20060078553-A1 Diverse multi-unit complexes including a tRNA synthetase fragment ANGIOSYN, INC. 2006-04-13 US disclosed
WO-2006016217-A1 tRNA SYNTHETASE FRAGMENTS ANGIOSYN, INC. (US) 2006-02-16 WO disclosed
US-20060024288-A1 tRNA synthetase fragments PFIZER INC. 2006-02-02 US disclosed
US-20060024286-A1 Variants of tRNA synthetase fragments and uses thereof ANGIOSYN, INC. 2006-02-02 US disclosed
US-20060024287-A1 Compositions and methods for modulating angiogenesis ANGIOSYN, INC. 2006-02-02 US disclosed
US-20060003933-A1 Compositions and methods for treatment of neovascular diseases NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2006-01-05 US disclosed
WO-2005117954-A2 COMPOSITIONS AND METHODS FOR TREATMENT OF NEOVASCULAR DISEASES THE SCRIPPS RESEARCH INSTITUTE (US) 2005-12-15 WO disclosed
WO-2005056754-A2 COMPOSITIONS AND METHODS TO REDUCE MUTAGENESIS THE SCRIPPS RESEARCH INSTITUTE (US) 2005-06-23 WO disclosed
US-6613753-B2 Restore cancer-suppressing functions to neoplastic cells through DNA hypomethylation SUPERGEN, INC. 2003-09-02 US disclosed
US-20020114809-A1 Restore cancer-suppressing functions to neoplastic cells through DNA hypomethylation ASTEX PHARMACEUTICALS, INC. 2002-08-22 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20160361337-A1 FORMULATIONS OF ACADESINE ADORA1, TNNC1, PDF GNRHR 3276/4885ABCC2 1413/4885PTGS1 424/4885
US-20060003933-A1 Compositions and methods for treatment of neovascular diseases TEK, KDR, WARS1 GNRHR 1770/4885ABCC2 3928/4885PTGS1 1692/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.