SCHEMBL960282

SCHEMBL960282

C[C@]12CC[C@@H]3c4cc(I)c(O)cc4CC[C@H]3[C@@H]1CC[C@H]2O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SHBG P04278 2/20 1.00
ESR1 P03372 5/20 0.82
ESR2 Q92731 4/20 0.82
LMNA P02545 3/20 0.82
MEN1 O00255 2/20 0.82
GAA P10253 2/20 0.82
MAPT P10636 2/20 0.82
KMT2A Q03164 2/20 0.82
KDM4E B2RXH2 1/20 0.82
POLB P06746 1/20 0.82
G6PD P11413 1/20 0.82
PKM P14618 1/20 0.82
MAPK1 P28482 1/20 0.82
RAB9A P51151 1/20 0.82
DAB2IP Q5VWQ8 1/20 0.82
ADCY10 Q96PN6 1/20 0.82
TDP1 Q9NUW8 1/20 0.82
CYP19A1 P11511 5/20 0.77
CYP1A2 P05177 3/20 0.72
HSD17B10 Q99714 3/20 0.72

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
SCHEMBL8584056 1.00 SHBG (1.00) SHBGESR1ESR2LMNAMEN1
SCHEMBL29565170 0.90 ESR1 (1.00) SHBGESR1ESR2LMNAMEN1
SCHEMBL225052 0.90 ESR1 (1.00) SHBGESR1ESR2LMNAMEN1
SCHEMBL13123058 0.90 ESR1 (1.00) SHBGESR1ESR2LMNAMEN1
SCHEMBL225053 0.90 ESR1 (1.00) SHBGESR1ESR2LMNAMEN1
SCHEMBL6010005 0.90 ESR1 (1.00) SHBGESR1ESR2LMNAMEN1
SCHEMBL15491309 0.90 ESR1 (1.00) SHBGESR1ESR2LMNAMEN1
SCHEMBL12027476 0.90 ESR1 (1.00) SHBGESR1ESR2LMNAMEN1
SCHEMBL4206797 0.87 CYP19A1 (1.00) SHBGESR1ESR2LMNAMEN1
SCHEMBL12820981 0.87 CYP19A1 (1.00) SHBGESR1ESR2LMNAMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109988209-B Enylated estradiol compound and preparation and application thereof 浙江工业大学 2020-08-28 CN disclosed
CN-101568547-B Substituted estratriene derivatives as 17 beta HSD inhibitors SOLVAY PHARM GMBH 2014-06-25 CN disclosed
US-8435973-B2 17-beta HSD1 and STS inhibitors ABBOTT PRODUCTS GMBH (DE) 2013-05-07 US disclosed
US-8288367-B2 Treatment or inhibition of a steroid hormone dependent disorder; reducing spermatogenesis or male virility; 17 beta -hydroxysteroid dehydrogenase (17 beta-HSD) inhibitors; compounds such as 3-(benzylamino)-15alpha-(4-morpholin-4-yl-4-oxobutyl)estra-1(10),2,4-trien-17-one SOLVAY PHARMACEUTICALS GMBH (DE) 2012-10-16 US disclosed
US-8030298-B2 17β-HSD1 and STS inhibitors ABBOTT PRODUCTS GMBH (DE) 2011-10-04 US disclosed
US-20110021480-A1 17-beta HSD1 and STS Inhibitors SOLVAY PHARMACEUTICALS GMBH (DE) 2011-01-27 US disclosed
CN-101568547-A Substituted estratriene derivatives as 17 beta HSD inhibitors SOLVAY PHARM GMBH (DE) 2009-10-28 CN disclosed
US-20080255075-A1 SUBSTITUTED ESTRATRIENE DERIVATIVES AS 17BETA HSD INHIBITORS SOLVAY PHARMACEUTICALS GMBH (DE) 2008-10-16 US disclosed
US-20070275935-A1 Estratriene Derivatives CRYPTOPHARMA PTY LTD (AU) 2007-11-29 US disclosed
US-20060281710-A1 17SS-HSD1 and STS inhibitors SOLVAY PHARMACEUTICALS GMBH 2006-12-14 US disclosed
CN-1867577-A Estratriene derivatives CRYPTOPHARMA PTY LTD (AU) 2006-11-22 CN disclosed
EP-1625143-A1 ESTRATRIENE DERIVATIVES Cryptopharma Pty Ltd (AU) 2006-02-15 EP disclosed
WO-2004101595-A1 ESTRATRIENE DERIVATIVES CRYPTOPHARMA PTY LTD (AU) 2004-11-25 WO disclosed
EP-0147155-A2 Improved method of preparing 2-Fluoro-17beta-estradiol ELI LILLY AND COMPANY (US) 1985-07-03 EP disclosed
US-4522758-A Method of preparing 2-fluoro-17β-estradiol ELI LILLY AND COMPANY (US) 1985-06-11 US disclosed
US-4205952-A METALLO-HAPTEN, METALLO-BINDER LABELLED COMPONENT TECHNION RESEARCH & DEVELOPMENT FOUNDATION LTD. (IL) 1980-06-03 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 (4 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-20080255075-A1 SUBSTITUTED ESTRATRIENE DERIVATIVES AS 17BETA HSD INHIBITORS HSD17B11, HSD17B1, HSD17B2 SHBG 26/4885ESR1 113/4885ESR2 57/4885
US-20060281710-A1 17SS-HSD1 and STS inhibitors HSD17B11, HSD17B1, STS SHBG 29/4885ESR1 88/4885ESR2 72/4885
US-20070275935-A1 Estratriene Derivatives ESR2, ESRRB, NR3C2 SHBG 62/4885ESR1 5/4885ESR2 1/4885
US-20110021480-A1 17-beta HSD1 and STS Inhibitors STS, HSD17B11, HSD17B1 SHBG 24/4885ESR1 206/4885ESR2 110/4885

“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.