SCHEMBL1659653

SCHEMBL1659653

CCN(CC)CCOC/C=C1\CC[C@H]2[C@@H]3[C@H](C)Cc4cc(O)ccc4[C@H]3CC[C@]12C

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
STS P08842 4/20 0.49
HRH3 Q9Y5N1 1/20 0.38
SIGMAR1 Q99720 1/20 0.37
HSD17B1 P14061 2/20 0.36
ESR1 P03372 12/20 0.36
ESR2 Q92731 8/20 0.36
HSD17B10 Q99714 4/20 0.36
CYP3A4 P08684 3/20 0.36
MAPT P10636 3/20 0.36
LMNA P02545 3/20 0.36
AKR1B10 O60218 2/20 0.36
SHBG P04278 2/20 0.36
CYP1A2 P05177 2/20 0.36
PGR P06401 2/20 0.36
SERPINA6 P08185 2/20 0.36
AR P10275 2/20 0.36
AKR1B1 P15121 2/20 0.36
SLC6A4 P31645 2/20 0.36
SNCA P37840 2/20 0.36
HTR2B P41595 2/20 0.36

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
SCHEMBL9945370 0.91 STS (0.40) STSHRH3SIGMAR1HSD17B1ESR1
SCHEMBL15804294 0.91 STS (0.40) STSHRH3SIGMAR1HSD17B1ESR1
SCHEMBL1659489 0.91 STS (0.40) STSHRH3SIGMAR1HSD17B1ESR1
SCHEMBL1659869 0.90 STS (0.40) STSHRH3SIGMAR1HSD17B1ESR1
SCHEMBL1657382 0.85 ESR1 (0.53) STSHSD17B1ESR1ESR2HSD17B10
SCHEMBL12225839 0.85 SIGMAR1 (0.37) STSHRH3SIGMAR1HSD17B1ESR1
SCHEMBL12225837 0.85 HRH3 (0.50) HRH3SIGMAR1HSD17B1ESR1ESR2
SCHEMBL12225841 0.84 HRH3 (0.49) HRH3SIGMAR1HSD17B1ESR1ESR2
SCHEMBL14396390 0.83 ESR1 (0.42) STSHSD17B1ESR1ESR2HSD17B10
SCHEMBL12225838 0.83 ESR1 (0.36) STSHRH3HSD17B1ESR1ESR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1847548-A2 Novel anti-estrogenic steroids, and associated pharmaceutical compositions and methods of use Sri International (US) 2007-10-24 EP claimed
US-6548491-B2 For therapy of conditions or diseases that are estrogen-dependent, i.e., are estrogen-induced or estrogen-stimulated SRI INTERNATIONAL 2003-04-15 US claimed
EP-2305694-A2 Novel anti-estrogenic steroids, and associated pharmaceutical compositions and methods of use SRI International (US) 2011-04-06 EP disclosed
EP-1847548-A2 Novel anti-estrogenic steroids, and associated pharmaceutical compositions and methods of use Sri International (US) 2007-10-24 EP disclosed
US-6747018-B2 TREATMENT OF ESTROGEN-DEPENDENT DISORDERS; PREFERRED COMPOUNDS HAVE 1,3,5-ESTRATRIENE NUCLEUS, AND ARE SUBSTITUTED AT C-17 OR C-11 WITH MOLECULAR MOIETY WHICH RENDERS COMPOUNDS EFFECTIVE TO BLOCK BINDING OF ESTROGEN TO ITS RECEPTOR SRI INTERNATIONAL 2004-06-08 US disclosed
US-20030153543-A1 Novel anti-estrogenic steroids, and associated pharmaceutical compositions and methods of use TANABE MASATO (US) 2003-08-14 US disclosed
EP-1310509-A2 Novel anti-estrogenic steroids, and associated pharmaceutical compositions and methods of use Sri International (US) 2003-05-14 EP disclosed
US-6548491-B2 For therapy of conditions or diseases that are estrogen-dependent, i.e., are estrogen-induced or estrogen-stimulated SRI INTERNATIONAL 2003-04-15 US disclosed
US-6503896-B1 17-Desoxy-1,3,5-estratriene derivatives; postmenopause, osteoporosis, central nervous system disorders; anticarcinogenic and hypotensive agents SRI INTERNATIONAL 2003-01-07 US disclosed
US-6455517-B1 FOR THERAPY OF CONDITIONS OR DISEASES THAT ARE ESTROGEN-DEPENDENT, I.E., ARE ESTROGEN-INDUCED OR ESTROGEN-STIMULATED SRI INTERNATIONAL 2002-09-24 US disclosed
US-20020032180-A1 Novel anti-estrogenic steroids, and associated pharmaceutical compositions and methods of use TANABE MASATO (US) 2002-03-14 US disclosed
US-20020032181-A1 Anti-estrogenic steroids, and associated pharmaceutical compositions and methods of use TANABE MASATO (US) 2002-03-14 US disclosed
US-6281205-B1 1,3,5(10)-ESTRATRIENE NUCLEUS, SUBSTITUTED AT THE C-17 POSITION WITH AN AMINE AND ETHER-CONTAINING GROUP SRI INTERNATIONAL 2001-08-28 US disclosed
US-6054446-A 17-SUBSTITUTED-17-DESOXY-1,3,5-ESTRATRIENES. SRI INTERNATIONAL (US) 2000-04-25 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 (3 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-20020032181-A1 Anti-estrogenic steroids, and associated pharmaceutical compositions and methods of use HSD17B11, ESR2, ESRRA STS 597/4885HRH3 2058/4885SIGMAR1 353/4885
US-20030153543-A1 Novel anti-estrogenic steroids, and associated pharmaceutical compositions and methods of use HSD17B11, ESR2, ESRRA STS 559/4885HRH3 2248/4885SIGMAR1 400/4885
US-20020032180-A1 Novel anti-estrogenic steroids, and associated pharmaceutical compositions and methods of use HSD17B11, ESR2, ESRRA STS 559/4885HRH3 2248/4885SIGMAR1 400/4885

“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.