Tamoxifen

Tamoxifen

SCHEMBL4465197

CCC(=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 SCHEMBL3794383 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 20 patents. 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
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
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-11337919-B2 Modified release drug powder composition comprising gastro-retentive RAFT forming systems having trigger pulse drug release TRIS PHARMA, INC. (US) 2022-05-24 US disclosed
US-20210015744-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING A FLOATING INTERPENETRATING POLYMER NETWORK FORMING SYSTEM PROVIDENT BANK 2021-01-21 US disclosed
US-20210015745-A1 MODIFIED RELEASE DRUG POWDER COMPOSITION COMPRISING GASTRO-RETENTIVE RAFT FORMING SYSTEMS HAVING TRIGGER PULSE DRUG RELEASE PROVIDENT BANK 2021-01-21 US disclosed
EP-3740189-A1 MODIFIED RELEASE DRUG POWDER COMPOSITION COMPRISING GASTRO-RETENTIVE RAFT FORMING SYSTEMS HAVING TRIGGER PULSE DRUG RELEASE Tris Pharma, Inc. (US) 2020-11-25 EP disclosed
EP-3740188-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING A FLOATING INTERPENETRATING POLYMER NETWORK FORMING SYSTEM Tris Pharma, Inc. (US) 2020-11-25 EP disclosed
EP-2815236-A1 MEANS AND METHODS FOR ASSESSING AN ENDOCRINE DISEASE OR DISORDER BASF SE (DE) 2014-12-24 EP disclosed
WO-2013121380-A1 MEANS AND METHODS FOR ASSESSING AN ENDOCRINE DISEASE OR DISORDER BASF SE (DE) 2013-08-22 WO disclosed
CN-102281903-A Method and formulation for reducing aggregation of a macromolecule under physiological conditions 2011-12-14 CN disclosed
WO-2009142968-A2 VALPROIC ACID SALTS OLEMA PHARMACEUTICALS, INC. (US) 2009-11-26 WO disclosed
WO-2006001035-A2 SYNERGISTIC LIPOSOMAL TAMOXIFEN COMPOSITION FOR TOPICAL APPLICATION AND METHOD OF PREPARING THEREOF. LIFECARE INNOVATIONS PVT. LTD. (IN) 2006-01-05 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-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