Bexarotene

Bexarotene

SCHEMBL9025

C=C(c1ccc(C(=O)O)cc1)c1cc2c(cc1C)C(C)(C)CCC2(C)C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

RXRARXRBRXRG

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RXRA known ✓ P19793 20/20 1.00
RXRB known ✓ P28702 7/20 1.00
RXRG known ✓ P48443 7/20 1.00
RARB P10826 6/20 1.00
RARG P13631 5/20 1.00
RARA P10276 3/20 1.00
MEN1 O00255 1/20 1.00
CYP26A1 O43174 1/20 1.00
ABCB11 O95342 1/20 1.00
ESR1 P03372 1/20 1.00
PGR P06401 1/20 1.00
HTR1A P08908 1/20 1.00
ADRA2A P08913 1/20 1.00
ADORA3 P0DMS8 1/20 1.00
CHRM1 P11229 1/20 1.00
DRD1 P21728 1/20 1.00
TBXA2R P21731 1/20 1.00
SLC6A2 P23975 1/20 1.00
ADRA1A P35348 1/20 1.00
OPRM1 P35372 1/20 1.00

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
Bexarotene SCHEMBL29412584 1.00 RXRA (1.00) RXRARXRBRXRGRARBRARG
Bexarotene SCHEMBL5322954 1.00 RXRA (1.00) RXRARXRBRXRGRARBRARG
Bexarotene SCHEMBL4432606 0.99 RXRA (0.97) RXRARXRBRXRGRARBRARG
Bexarotene SCHEMBL28672173 0.97 RXRA (0.94) RXRARXRBRXRGRARBRARG
SCHEMBL24055307 0.95 RXRA (0.90) RXRARXRBRXRGRARBRARG
SCHEMBL24055118 0.95 RXRA (0.90) RXRARXRBRXRGRARBRARG
Bexarotene SCHEMBL2571575 0.93 RXRA (0.87) RXRARXRBRXRGRARBRARG
SCHEMBL16926899 0.91 RXRA (0.84) RXRARXRBRXRGRARBRARG
SCHEMBL6891228 0.91 RXRA (0.84) RXRARXRBRXRGRARBRARG
SCHEMBL19119460 0.90 RXRA (0.81) RXRARXRBRXRGRARBRARG

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 43856 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026104588-A1 UROLITHIN COMBINATION AMAZENTIS SA (CH) 2026-05-21 WO 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
CN-122057026-A Pharmaceutical composition for treating multiple myeloma and application thereof 南京鼓楼医院 2026-05-19 CN claimed
US-20260132141-A1 PROTEIN PHOSPHATASE 2A ACTIVATORS UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) 2026-05-14 US claimed
EP-4741421-A1 FAB-ARM EXCHANGE-PREVENTING FC VARIANTS FROM WHICH EFFECTOR FUNCTIONS ARE REMOVED Korea University Research and Business Foundation (KR) 2026-05-13 EP claimed
US-20260108476-A1 2,4 DNP and Prodrugs Thereof for Treatment of Cancer MITOCHON PHARMACEUTICALS, INC. (US) 2026-04-23 US claimed
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS HANGZHOU DAC BIOTECH CO., LTD. (CN) 2026-04-23 US claimed
EP-4727596-A2 ANTIBODY-DRUG CONJUGATES AND LINKERS AND METHODS OF USE THEREOF Ohio State Innovation Foundation (US) 2026-04-22 EP claimed
EP-3515892-B1 COMPOUNDS AND METHODS FOR IDO AND TDO MODULATION, AND INDICATIONS THEREFOR PLEXXIKON INC (US) 2026-04-15 EP claimed
EP-0983992-A2 Compounds having selectivity for retinoid x receptors LIGAND PHARMACEUTICALS, INC. (US) 2000-03-08 EP claimed
US-6028088-A USEFUL AS ANTIPROLIFERATIVE, ANTIINFLAMMATORY AND ANTIINFECTIVE AGENTS; FOR TREATMENT OF CERTAIN ENDOCRINE DISEASES INCLUDING DIABETES, CERTAIN MALIGNANT AND NON-MALIGNANT PROLIFERATIVE DISEASES INCLUDING PROSTATE CANCER THE UNIVERSITY OF MISSISSIPPI (US) 2000-02-22 US claimed
US-6025133-A NUCLEIC ACID SEQUENCE INCLUDING A RNA POLYMERASE PROMOTER; FORMS A STEM-LOOP STRUCTURE IN THE ABSENCE OF TARGET SEQUENCE; FOR AMPLIFYING NUCLEIC ACID USING A TARGET NUCLEIC ACID SEQUENCE TO TRIGGER TRANSCRIPTION; DIAGNOSTIC TESTS GEN-PROBE INCORPORATED (US) 2000-02-15 US claimed
EP-0963199-A1 TREATMENT OF DISEASE STATES WHICH RESULT FROM NEOPLASTIC CELL PROLIFERATION USING PPAR-GAMMA ACTIVATORS AND COMPOSITIONS USEFUL THEREFOR THE SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) 1999-12-15 EP claimed
WO-1999058155-A1 FORMULATIONS USEFUL FOR MODULATING EXPRESSION OF EXOGENOUS GENES IN MAMMALIAN SYSTEMS, AND PRODUCTS RELATED THERETO THE SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) 1999-11-18 WO claimed
WO-1998029120-A1 TREATMENT OF LIPOSARCOMAS USING A COMBINATION OF THIAZOLIDINEDIONES AND RETINOID X RECEPTOR SELECTIVE AGONISTS THE SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) 1998-07-09 WO claimed
WO-1998029113-A1 TREATMENT OF DISEASE STATES WHICH RESULT FROM NEOPLASTIC CELL PROLIFERATION USING PPAR-GAMMA ACTIVATORS AND COMPOSITIONS USEFUL THEREFOR THE SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) 1998-07-09 WO claimed
EP-0637297-A1 COMPOUNDS HAVING SELECTIVITY FOR RETINOID X RECEPTORS LIGAND PHARMACEUTICALS, INC. (US) 1995-02-08 EP claimed
WO-1993021146-A1 COMPOUNDS HAVING SELECTIVITY FOR RETINOID X RECEPTORS LIGAND PHARMACEUTICALS INCORPORATED (US) 1993-10-28 WO claimed
EP-0254122-B1 METHOD FOR INCREASING THE HIT PROBABILITY OF MULTIPLE-TUBE MACHINE GUNS Mauser-Werke Oberndorf GmbH (DE) 1990-07-04 EP claimed