Abiraterone

Abiraterone

SCHEMBL61108

C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ARCYP17A1SRD5A1SRD5A2SRD5A3

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

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
CYP17A1 known ✓ P05093 16/20 1.00
AR known ✓ P10275 1/20 0.71
CYP21A2 P08686 6/20 1.00
CYP11B1 P15538 2/20 1.00
CYP3A4 P08684 1/20 1.00
CYP11B2 P19099 1/20 1.00
CDK8 P49336 3/20 0.72
PGR P06401 1/20 0.71

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
Abiraterone SCHEMBL16383633 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP11B2
Abiraterone SCHEMBL17474701 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP11B2
Abiraterone SCHEMBL20459184 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP11B2
Abiraterone SCHEMBL23924960 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP11B2
Abiraterone SCHEMBL8736929 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP11B2
Abiraterone SCHEMBL25074918 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP11B2
Abiraterone SCHEMBL13272100 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP11B2
Abiraterone SCHEMBL19724576 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP11B2
Abiraterone SCHEMBL22414103 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP11B2
Abiraterone SCHEMBL15700283 1.00 CYP17A1 (1.00) CYP17A1CYP21A2CYP11B1CYP3A4CYP11B2

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 24639 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4746850-A1 EXTENDED RELEASE DRUG-LOADED MICROPARTICLES Ferring BV (NL) 2026-05-27 EP claimed
EP-3433239-B1 SMALL MOLECULE INHIBITORS OF THE NUCLEAR TRANSLOCATION OF ANDROGEN RECEPTOR FOR THE TREATMENT OF CASTRATION-RESISTANT PROSTATE CANCER UNIV PITTSBURGH COMMONWEALTH SYS HIGHER EDUCATION (US) 2026-05-27 EP claimed
EP-3946313-B1 ONVANSERTIB FOR THE TREATMENT OF METASTATIC CASTRATION-RESISTANT PROSTATE CANCER CARDIFF ONCOLOGY INC (US) 2026-05-27 EP claimed
CN-120504685-B Prodrug structure with ROS signal response performance, and preparation method and application thereof Rehabilitation University (CN) 2026-05-26 CN claimed
WO-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO claimed
EP-3841097-B1 2,6-BIS(((1H-BENZO[D]IMIDAZOL-2-YL)THIO)METHYL)PYRIDINE AND N2,N6-DIBENZYLPYRIDINE-2,6-DICARBOXAMIDE DERIVATIVES AND RELATED COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE (PI3K) INHIBITORS FOR TREATING CANCER BIOMEDICAL RES FOUNDATION OF THE ACADEMY OF ATHENS BRFAA (GR) 2026-05-20 EP claimed
EP-4744666-A1 PHARMACEUTICAL COMPOSITION AND USE THEREOF TransThera Sciences (Nanjing), Inc. (CN) 2026-05-20 EP claimed
CN-122060013-A L-valine abiraterone p-toluenesulfonic acid crystal form and preparation method thereof 山东新时代药业有限公司 2026-05-19 CN claimed
CN-122060014-A Salt of abiraterone derivative and preparation method thereof 山东新时代药业有限公司 2026-05-19 CN claimed
US-20260130856-A1 LIPOSOME COMPOSITIONS FOR DELIVERY OF COMPOUNDS AND METHODS THEREOF NANOTECH PHARMA INC (US) 2026-05-14 US claimed
EP-1556058-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING ESTETROL DERIVATIVES FOR USE IN CANCER THERAPY Pantarhei Bioscience B.V. (NL) 2005-07-27 EP claimed
US-20040092583-A1 Treatment for inhibiting neoplastic lesions SHANAHAN-PRENDERGAST ELIZABETH (IE) 2004-05-13 US claimed
WO-2004037269-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING ESTETROL DERIVATIVES FOR USE IN CANCER THERAPY PANTARHEI BIOSCIENCE B.V. (NL) 2004-05-06 WO claimed
EP-1351678-A2 TREATMENT FOR INHIBITING NEOPLASTIC LESIONS USING INCENSOLE AND/OR FURANOGERMACRENS Shanahan-Prendergast, Elizabeth (IE) 2003-10-15 EP claimed
EP-1336602-A1 Nitrate prodrugs able to release nitric oxide in a controlled and selective way and their use for prevention and treatment of inflammatory, ischemic and proliferative diseases Scaramuzzino, Giovanni (IT) 2003-08-20 EP claimed
WO-2002053138-A2 TREATMENT FOR INHIBITING NEOPLASTIC LESIONS USING INCENSOLE AND/OR FURANOGERMACRENS SHANAHAN-PRENDERGAST ELISABETH (IE) 2002-07-11 WO claimed
EP-0633893-B1 17-SUBSTITUTED STEROIDS USEFUL IN CANCER TREATMENT BTG INT LTD (GB) 1999-11-24 EP claimed
JP-2742331-B2 1998-04-22 JP claimed
EP-0633893-A1 17-SUBSTITUTED STEROIDS USEFUL IN CANCER TREATMENT BRITISH TECHNOLOGY GROUP LTD (GB) 1995-01-18 EP claimed
WO-1993020097-A1 17-SUBSTITUTED STEROIDS USEFUL IN CANCER TREATMENT BRITISH TECHNOLOGY GROUP LTD. (GB) 1993-10-14 WO claimed