Tamoxifen

Tamoxifen

SCHEMBL1056785

CC/C(=C(/c1ccccc1)c1ccc(OCCN(C)C)cc1)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 1.00
ESR2 Q92731 6/20 1.00
MAPT P10636 3/20 1.00
MEN1 O00255 3/20 1.00
TP53 P04637 3/20 1.00
CYP3A4 P08684 3/20 1.00
KMT2A Q03164 3/20 1.00
ESRRG P62508 3/20 1.00
PGR P06401 2/20 1.00
CYP1A2 P05177 2/20 1.00
CYP2D6 P10635 2/20 1.00
HTR6 P50406 2/20 1.00
NPC1 O15118 1/20 1.00
NR1I2 O75469 1/20 1.00
PRKD3 O94806 1/20 1.00
ABCB11 O95342 1/20 1.00
EGFR P00533 1/20 1.00
GBA1 P04062 1/20 1.00
NR3C1 P04150 1/20 1.00
ERBB2 P04626 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
Tamoxifen SCHEMBL119181 1.00 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL17262082 1.00 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
SCHEMBL29659348 1.00 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL4084 1.00 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL4085 1.00 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL17262111 1.00 ESR1 (1.00) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL5789295 0.99 ESR1 (0.97) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL3794383 0.99 ESR1 (0.97) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL4323848 0.99 ESR1 (0.97) ESR1ESR2MAPTMEN1TP53
Tamoxifen SCHEMBL4323842 0.99 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 262 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12280059-B2 Acyl-CoA synthetase 4 (ACSL4) inhibitory compound CONSEJO NACIONAL DE INVESTIGACIONES CIENTÍFICAS Y TÉCNICAS (CONICET) (AR) 2025-04-22 US claimed
EP-3927434-B1 ACYL-COA SYNTHETASE 4 (ACSL4) INHIBITORY COMPOUND CONSEJO NACIONAL DE INVESTIGACIONES CIENTIFICAS Y TECN CONICET (AR) 2024-10-16 EP claimed
CN-113278598-B Biological enzyme system for preparing drug metabolites and application thereof 山东大学 2022-08-30 CN claimed
CN-114929708-A 4- [ [ (7-aminopyrazolo [1,5-A ] pyrimidin-5-yl) amino ] methyl ] piperidin-3-ol compounds and their therapeutic use 卡里克治疗有限公司 2022-08-19 CN claimed
US-20220133731-A1 ACYL-COA SYNTHETASE 4 (ACSL4) INHIBITORY COMPOUND CONSEJO NACIONAL DE INVESTIGACIONES CIENTÍFICAS Y TÉCNICAS (CONICET) (AR) 2022-05-05 US claimed
EP-0710116-B1 PREVENTION AND TREATMENT OF PATHOLOGIES ASSOCIATED WITH ABNORMALLY PROLIFERATIVE SMOOTH MUSCLE CELLS PONIARD PHARMACEUTICALS INC (US) 2008-09-03 EP claimed
EP-1510220-B1 Therapeutic inhibitor of vascular smooth muscle cells PONIARD PHARMACEUTICALS INC (US) 2008-07-23 EP claimed
US-7393864-B2 Use of ClC3 chloride channel blockers to modulate vascular tone UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2008-07-01 US claimed
US-7220782-B1 Methods to reduce the sensitivity of endothelially-compromised vascular smooth muscle UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2007-05-22 US claimed
US-20060100168-A1 Method of treating cancer using adenosine and its analogs THE TRUSTEE OF BOSTON UNIVERSITY (US) 2006-05-11 US claimed
EP-0702557-A1 THERAPEUTIC INHIBITOR OF VASCULAR SMOOTH MUSCLE CELLS NEORX CORPORATION (US) 1996-03-27 EP claimed
US-5472985-A Prevention and treatment of pathologies associated with abnormally proliferative smooth muscle cells NEORX CORPORATION (US) 1995-12-05 US claimed
WO-1994026291-A1 THERAPEUTIC INHIBITOR OF VASCULAR SMOOTH MUSCLE CELLS NEORX CORPORATION (US) 1994-11-24 WO claimed
WO-1994026303-A1 PREVENTION AND TREATMENT OF PATHOLOGIES ASSOCIATED WITH ABNORMALLY PROLIFERATIVE SMOOTH MUSCLE CELLS NEORX CORPORATION (US) 1994-11-24 WO claimed
EP-0153160-B1 NOVEL CYTOTOXIC AMINOALKYL PHENOL ETHERS The University of Manitoba (CA) 1989-05-10 EP claimed
US-4803227-A N,N-DIALKYL-2-//4-PHENYLMETHYL/PHENOXY/ETHANAMINE AND TAMOXIFE N THE UNIVERSITY OF MANITOBA (CA) 1989-02-07 US 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-0153160-A1 Novel cytotoxic aminoalkyl phenol ethers The University of Manitoba (CA) 1985-08-28 EP claimed
US-4536516-A Alkene derivatives IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1985-08-20 US 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

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-12280059-B2 Acyl-CoA synthetase 4 (ACSL4) inhibitory compound ACSL4, ACSL3, ACSL1 ESR1 548/4885ESR2 813/4885MAPT 3159/4885
US-20220133731-A1 ACYL-COA SYNTHETASE 4 (ACSL4) INHIBITORY COMPOUND ACSL4, ACSL3, ACSL1 ESR1 548/4885ESR2 813/4885MAPT 3159/4885

“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.