Dienestrol

Dienestrol

SCHEMBL8854079

C/C=C(C(=C/C)/c1ccc(O)cc1)\c1ccc(O)cc1.C[Si](C)(C)O[Si](C)(C)C

nearest known ligand 0.71

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ESR1

The experimentally established mechanism targets of Dienestrol. 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 10/20 0.71
MAPT P10636 6/20 0.71
LMNA P02545 4/20 0.71
HSD17B10 Q99714 4/20 0.71
MEN1 O00255 4/20 0.71
KMT2A Q03164 4/20 0.71
TP53 P04637 3/20 0.71
CYP3A4 P08684 3/20 0.71
ALOX15 P16050 3/20 0.71
HIF1A Q16665 3/20 0.71
NR3C1 P04150 2/20 0.71
CYP1A2 P05177 2/20 0.71
ADORA3 P0DMS8 2/20 0.71
CYP2D6 P10635 2/20 0.71
CYP2C9 P11712 2/20 0.71
CYP2C19 P33261 2/20 0.71
OPRD1 P41143 2/20 0.71
GAA P10253 1/20 0.71
ALOX12 P18054 1/20 0.71
CA12 O43570 4/20 0.38

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
Dienestrol SCHEMBL2896848 0.84 ESR1 (1.00) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL52170 0.84 ESR1 (1.00) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL2896853 0.84 ESR1 (1.00) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL6573104 0.82 ESR1 (0.85) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL8425094 0.82 ESR1 (0.85) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL9317394 0.82 ESR1 (0.94) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL5689185 0.81 ESR1 (0.61) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL114016 0.80 ESR1 (0.81) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL3716190 0.80 ESR1 (0.90) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL5691782 0.79 ESR1 (0.63) ESR1MAPTLMNAHSD17B10MEN1

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5597931-A Total synthesis of taxol and analogues thereof SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1997-01-28 US disclosed
WO-1996034862-A1 TOTAL SYNTHESIS OF TAXOL AND ANALOGUES THEREOF SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1996-11-07 WO disclosed
US-5527924-A ANTICARCINOGENIC AGENTS SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1996-06-18 US disclosed
US-5488116-A Total synthesis of taxol and analogues thereof SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1996-01-30 US disclosed
US-5416225-A Chemical intermediates SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1995-05-16 US disclosed
WO-1995012567-A1 TOTAL SYNTHESIS OF TAXOL AND ANALOGUES THEREOF SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1995-05-11 WO disclosed
WO-1993020036-A1 TOTAL SYNTHESIS OF TAXOL SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1993-10-14 WO disclosed