SCHEMBL6689499

SCHEMBL6689499

C=C1C[C@]2(CC)C(=O)CC[C@H]2[C@@H]2CCC3=CCCC[C@@H]3[C@@H]12

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ESR1 P03372 4/20 0.55
▸ PGR P06401 4/20 0.55
▸ AR P10275 3/20 0.55
▸ CHRM2 P08172 3/20 0.55
▸ SLC6A2 P23975 3/20 0.55
▸ SLC6A4 P31645 3/20 0.55
▸ SHBG P04278 2/20 0.55
▸ OPRM1 P35372 2/20 0.55
▸ ADORA3 P0DMS8 2/20 0.55
▸ PTGS1 P23219 2/20 0.55
▸ SLC6A3 Q01959 2/20 0.55
▸ NR1I2 O75469 1/20 0.55
▸ NR3C1 P04150 1/20 0.55
▸ DRD1 P21728 1/20 0.55
▸ AGTR1 P30556 1/20 0.55
▸ CCKBR P32239 1/20 0.55
▸ DRD3 P35462 1/20 0.55
▸ PDE4D Q08499 1/20 0.55
▸ KCNH2 Q12809 1/20 0.55
▸ CYP2C19 P33261 2/20 0.40

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
SCHEMBL20851704 1.00 ESR1 (0.55) ESR1PGRARCHRM2SLC6A2
SCHEMBL20851686 1.00 ESR1 (0.55) ESR1PGRARCHRM2SLC6A2
SCHEMBL20851607 0.89 ESR1 (0.45) ESR1PGRARCHRM2SLC6A2
SCHEMBL8410551 0.89 ESR1 (0.45) ESR1PGRARCHRM2SLC6A2
SCHEMBL20851698 0.83 PGR (0.57) ESR1PGRARCHRM2SLC6A2
SCHEMBL14946855 0.83 PGR (0.57) ESR1PGRARCHRM2SLC6A2
SCHEMBL9194138 0.83 PGR (0.57) ESR1PGRARCHRM2SLC6A2
SCHEMBL9547849 0.83 ESR1 (0.50) ESR1PGRARCHRM2SLC6A2
SCHEMBL14946875 0.82 SHBG (0.41) ESR1PGRARCHRM2SLC6A2
SCHEMBL11150692 0.81 ESR1 (0.49) ESR1PGRARCHRM2SLC6A2

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
CN-114057819-A Method for recovering desogestrel recrystallization mother liquor 上海共拓医药化工有限公司 2022-02-18 — — CN claimed
CN-114057819-A Method for recovering desogestrel recrystallization mother liquor 上海共拓医药化工有限公司 2022-02-18 — — CN disclosed
US-7667056-B2 Desogestrel synthesis characterized by regioselective reduction of a diketo intermediate 18-methyl-11-hydroxyestr-4-en-3,17-dione; higher yields, easier purification POLI INDUSTRIA CHIMICA S.P.A. (IT) 2010-02-23 — — US disclosed
US-7667056-B2 Desogestrel synthesis characterized by regioselective reduction of a diketo intermediate 18-methyl-11-hydroxyestr-4-en-3,17-dione; higher yields, easier purification POLI INDUSTRIA CHIMICA S.P.A. (IT) 2010-02-23 — — US disclosed
WO-2009033499-A1 TOTAL SYNTHESIS OF ENANTIOPURE DESOGESTREL Georg-August-Universität Göttingen Stiftung Öffentlichen Rechts (DE) 2009-03-19 — — WO disclosed
WO-2004101594-A1 NEW MONO-AND BISMETHYLENE-STEROID DERIVATIVES AND PROCESS FOR THEIR SYNTHESIS Richter Gedeon Vegyészeti Gyár Rt. (HU) 2004-11-25 — — WO disclosed
EP-0643070-B1 Steroid intermediates and process for their preparation JENAPHARM GMBH (DE) 1999-07-21 — — EP disclosed
US-5831104-A Steroid intermediate products and method of their production JENAPHARM GMBH (DE) 1998-11-03 — — US disclosed
EP-0643070-A1 Steroid intermediates and process for their preparation JENAPHARM GmbH (DE) 1995-03-15 — — EP disclosed
EP-0440752-B1 METHOD FOR THE PREPARATION OF 3-DESOXY-4-ENE STEROIDS SCHERING AG (DE) 1995-03-08 — — EP disclosed
US-5140106-A PROCESS FOR THE PRODUCTION OF 3-DEOXY-4-ENE STEROIDS SCHERING AKTIENGESELLSCHAFT (DE) 1992-08-18 — — US disclosed
EP-0440752-A1 METHOD FOR THE PREPARATION OF 3-DESOXY-4-ENE STEROIDS. SCHERING AG (DE) 1991-08-14 — — EP disclosed
WO-1990011290-A1 METHOD FOR THE PREPARATION OF 3-DESOXY-4-ENE STEROIDS SCHERING AKTIENGESELLSCHAFT (DE) 1990-10-04 — — WO disclosed
US-4277468-A CONTRACEPTIVES, PROGESTATIONAL ACTIVITY SCHERING AKTIENGESELLSCHAFT (DE) 1981-07-07 — — US disclosed
Send feedback