Tamoxifen

Tamoxifen

SCHEMBL3794383

CC/C(=C(\c1ccccc1)c1ccc(OCCN(C)C)cc1)c1ccccc1.Cl

nearest known ligand 0.97

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ESR1

The experimentally established mechanism targets of Tamoxifen. 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
ESR1 known ✓ P03372 8/20 0.97
ESR2 Q92731 6/20 0.97
MAPT P10636 3/20 0.97
MEN1 O00255 3/20 0.97
TP53 P04637 3/20 0.97
CYP3A4 P08684 3/20 0.97
KMT2A Q03164 3/20 0.97
ESRRG P62508 3/20 0.97
PGR P06401 2/20 0.97
CYP1A2 P05177 2/20 0.97
CYP2D6 P10635 2/20 0.97
HTR6 P50406 2/20 0.97
NPC1 O15118 1/20 0.97
NR1I2 O75469 1/20 0.97
PRKD3 O94806 1/20 0.97
ABCB11 O95342 1/20 0.97
EGFR P00533 1/20 0.97
GBA1 P04062 1/20 0.97
NR3C1 P04150 1/20 0.97
ERBB2 P04626 1/20 0.97

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
Tamoxifen SCHEMBL4465197 1.00 ESR1 (0.97) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL119181 0.99 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
SCHEMBL29659348 0.99 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL17262082 0.99 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL1056785 0.99 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL4084 0.99 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL4085 0.99 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL17262111 0.99 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL3046696 0.97 ESR1 (0.97) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL4323848 0.97 ESR1 (0.97) ESR1ESR2MAPTMEN1TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109153656-B Crystal form E of tadalafil tamibamide salt and preparation method and application thereof 苏州晶云药物科技股份有限公司 2021-06-25 CN claimed
EP-0127128-B1 PROCESS FOR THE CONVERSION OF THE E ISOMER OF 1,2-DIPHENYL-1-(4-(2-DIMETHYLAMINOETHOXY)-PHENYL)-1-BUTENE TO TAMOXIFEN HCL Bristol-Myers Company (US) 1987-02-25 EP claimed
EP-0127128-A1 Process for the conversion of the E isomer of 1,2-diphenyl-1-(4-(2-dimethylaminoethoxy)-phenyl)-1-butene to tamoxifen HCl Bristol-Myers Company (US) 1984-12-05 EP claimed
US-20250304916-A1 METHODS AND COMPOSITIONS FOR GENERATING VASCULAR LEPTOMENINGEAL CELLS TRAILHEAD BIOSYSTEMS INC (US) 2025-10-02 US disclosed
US-20240060950-A1 QUANTITATION OF TAMOXIFEN AND METABOLITES THEREOF BY MASS SPECTROMETRY QUEST DIAGNOSTICS INVESTMENTS LLC (US) 2024-02-22 US disclosed
US-11835505-B2 Quantitation of tamoxifen and metabolites thereof by mass spectrometry QUEST DIAGNOSTICS INVESTMENTS INCORPORATED (US) 2023-12-05 US disclosed
CN-116940351-A Prodrug compositions and methods of treatment 阿奎斯蒂弗医疗股份有限公司 2023-10-24 CN disclosed
EP-4220178-A2 QUANTITATION OF TAMOXIFEN AND METABOLITES THEREOF BY MASS SPECTROMETRY Quest Diagnostics Investments Incorporated (US) 2023-08-02 EP disclosed
US-20230114103-A1 QUANTITATION OF TAMOXIFEN AND METABOLITES THEREOF BY MASS SPECTROMETRY QUEST DIAGNOSTICS INVESTMENTS INCORPORATED (US) 2023-04-13 US disclosed
EP-3143392-B1 QUANTITATION OF TAMOXIFEN METABOLITES BY MASS SPECTROMETRY QUEST DIAGNOSTICS INVEST INC (US) 2023-02-22 EP disclosed
US-20220241189-A1 MODIFIED RELEASE DRUG POWDER COMPOSITION COMPRISING GASTRO-RETENTIVE RAFT FORMING SYSTEMS HAVING TRIGGER PULSE DRUG RELEASE PROVIDENT BANK 2022-08-04 US disclosed
US-20040115132-A1 Protein cages for the delivery of medical imaging and therapeutic agents NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2004-06-17 US disclosed
WO-1996009051-A1 A METHOD FOR MINIMIZING THE UTEROTROPHIC EFFECT OF TAMOXIFEN AND TAMOXIFEN ANALOGS ELI LILLY AND COMPANY (US) 1996-03-28 WO disclosed
EP-0126470-B1 PROCESS FOR THE PREPARATION OF TAMOXIFEN Bristol-Myers Company (US) 1989-04-12 EP disclosed
EP-0127128-B1 PROCESS FOR THE CONVERSION OF THE E ISOMER OF 1,2-DIPHENYL-1-(4-(2-DIMETHYLAMINOETHOXY)-PHENYL)-1-BUTENE TO TAMOXIFEN HCL Bristol-Myers Company (US) 1987-02-25 EP disclosed
EP-0127128-B1 PROCESS FOR THE CONVERSION OF THE E ISOMER OF 1,2-DIPHENYL-1-(4-(2-DIMETHYLAMINOETHOXY)-PHENYL)-1-BUTENE TO TAMOXIFEN HCL Bristol-Myers Company (US) 1987-02-25 EP disclosed
EP-0127128-A1 Process for the conversion of the E isomer of 1,2-diphenyl-1-(4-(2-dimethylaminoethoxy)-phenyl)-1-butene to tamoxifen HCl Bristol-Myers Company (US) 1984-12-05 EP disclosed
EP-0127128-A1 Process for the conversion of the E isomer of 1,2-diphenyl-1-(4-(2-dimethylaminoethoxy)-phenyl)-1-butene to tamoxifen HCl Bristol-Myers Company (US) 1984-12-05 EP disclosed
EP-0127128-A1 Process for the conversion of the E isomer of 1,2-diphenyl-1-(4-(2-dimethylaminoethoxy)-phenyl)-1-butene to tamoxifen HCl Bristol-Myers Company (US) 1984-12-05 EP disclosed
EP-0126470-A1 Process for the preparation of tamoxifen Bristol-Myers Company (US) 1984-11-28 EP disclosed