Dienestrol

Dienestrol

SCHEMBL6573104

C/C=C(C(=C/C)/c1ccc(O)cc1)\c1ccc(O)cc1.OOO

nearest known ligand 0.85

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 7/20 0.85
MAPT P10636 5/20 0.85
LMNA P02545 4/20 0.85
HSD17B10 Q99714 4/20 0.85
MEN1 O00255 3/20 0.85
CYP3A4 P08684 3/20 0.85
ALOX15 P16050 3/20 0.85
KMT2A Q03164 3/20 0.85
HIF1A Q16665 3/20 0.85
NR3C1 P04150 2/20 0.85
TP53 P04637 2/20 0.85
CYP1A2 P05177 2/20 0.85
ADORA3 P0DMS8 2/20 0.85
CYP2D6 P10635 2/20 0.85
CYP2C9 P11712 2/20 0.85
CYP2C19 P33261 2/20 0.85
OPRD1 P41143 2/20 0.85
GAA P10253 1/20 0.85
ALOX12 P18054 1/20 0.85
CA12 O43570 5/20 0.43

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 SCHEMBL2896853 0.92 ESR1 (1.00) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL2896848 0.92 ESR1 (1.00) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL52170 0.92 ESR1 (1.00) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL8425094 0.90 ESR1 (0.85) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL9317394 0.90 ESR1 (0.94) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL114016 0.88 ESR1 (0.81) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL3716190 0.87 ESR1 (0.90) ESR1MAPTLMNAHSD17B10MEN1
SCHEMBL13492676 0.83 MAPT (0.81) ESR1MAPTLMNAHSD17B10MEN1
SCHEMBL15721373 0.82 MAPT (0.71) ESR1MAPTLMNAHSD17B10MEN1
Dienestrol SCHEMBL8854079 0.82 ESR1 (0.71) 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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1409512-A1 20-FLUORO-17(20)-VINYL STEROIDS AS INHIBITORS OF C17-20-LYASE AND 5-ALPHA REDUCTASE Aventis Pharma S.A. (FR) 2004-04-21 EP disclosed
US-6413951-B2 ENZYME INHIBITOR AVENTIS PHARMACEUTICALS, INC. 2002-07-02 US disclosed
US-20020019548-A1 20-Fluoro-17(20)-vinyl steroids AVENTIS PHARMA S.A. (FR) 2002-02-14 US disclosed
WO-2002000681-A1 20-FLUORO-17(20)-VINYL STEROIDS AS INHIBITORS OF C17-20-LYASE AND 5-ALPHA REDUCTASE AVENTIS PHARMA S.A. (FR) 2002-01-03 WO disclosed
US-4080334-A Intermediates in the total synthesis employing substituted isoxazole derivatives HOFFMANN-LA ROCHE INC. (US) 1978-03-21 US disclosed
US-4044004-A Total steroid synthesis employing substituted isoxazole derivatives HOFFMANN-LA ROCHE INC. (US) 1977-08-23 US disclosed
US-3985771-A Total steroid synthesis employing substituted isoxazole derivatives HOFFMANN-LA ROCHE INC. (US) 1976-10-12 US disclosed
US-3984428-A Isoxazolyl-substituted perhydrobenzindenes HOFFMANN-LA ROCHE INC. (US) 1976-10-05 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 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-20020019548-A1 20-Fluoro-17(20)-vinyl steroids CYP17A1, HSD17B11, HSD3B1 ESR1 111/4885MAPT 2727/4885LMNA 4392/4885

“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.