SCHEMBL4539514

SCHEMBL4539514

CC(=O)[C@@]12O[C@@H]1C[C@H]1[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@@]12C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP17A1 P05093 3/20 1.00
▸ SERPINA6 P08185 6/20 0.66
▸ SHBG P04278 7/20 0.65
▸ LMNA P02545 6/20 0.65
▸ SMN1; SMN2 Q16637 6/20 0.65
▸ BLM P54132 4/20 0.65
▸ NR3C1 P04150 3/20 0.65
▸ MAPT P10636 3/20 0.65
▸ CYP2C19 P33261 3/20 0.65
▸ MEN1 O00255 2/20 0.65
▸ ADORA3 P0DMS8 2/20 0.65
▸ KMT2A Q03164 2/20 0.65
▸ MAPK3 P27361 1/20 0.65
▸ SLC6A3 Q01959 1/20 0.65
▸ ALDH1A1 P00352 5/20 0.60
▸ PGR P06401 2/20 0.60
▸ ADRA1A P35348 2/20 0.60
▸ HTR2B P41595 2/20 0.60
▸ CYP3A4 P08684 5/20 0.56
▸ TSHR P16473 4/20 0.56

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
SCHEMBL29409283 1.00 CYP17A1 (1.00) CYP17A1SERPINA6SHBGLMNASMN1; SMN2
SCHEMBL29500568 1.00 CYP17A1 (1.00) CYP17A1SERPINA6SHBGLMNASMN1; SMN2
SCHEMBL4541005 1.00 CYP17A1 (1.00) CYP17A1SERPINA6SHBGLMNASMN1; SMN2
SCHEMBL7993136 1.00 CYP17A1 (1.00) CYP17A1SERPINA6SHBGLMNASMN1; SMN2
Algestone Acetonide SCHEMBL42582 0.92 CYP17A1 (0.85) CYP17A1SERPINA6SHBGLMNASMN1; SMN2
SCHEMBL151266 0.87 CYP17A1 (0.76) CYP17A1SERPINA6SHBGLMNASMN1; SMN2
Algestone Acetophenide SCHEMBL1649218 0.87 CYP17A1 (0.76) CYP17A1SERPINA6SHBGLMNASMN1; SMN2
Algestone Acetophenide SCHEMBL3039564 0.87 CYP17A1 (0.76) CYP17A1SERPINA6SHBGLMNASMN1; SMN2
Algestone Acetophenide SCHEMBL282250 0.87 CYP17A1 (0.76) CYP17A1SERPINA6SHBGLMNASMN1; SMN2
SCHEMBL27759498 0.85 CYP17A1 (0.73) CYP17A1SERPINA6SHBGLMNASMN1; SMN2

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 93 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118879822-A Conversion method of 11 a-hydroxy-16, 17 epoxyprogesterone 佳尔科生物科技南通有限公司 2024-11-01 — — CN claimed
CN-105483028-B It is a kind of to synthesize 11 α, the method for 15 α-diOH- 16ALPHA,17ALPHA-epoxyprogesterones using gibberella 江南大学 2019-01-08 — — CN claimed
CN-207187707-U A kind of oxidation reaction apparatus for producing 16ALPHA,17ALPHA-epoxyprogesterone 湖北丹澳药业有限公司 2018-04-06 — — CN claimed
CN-104610421-B The synthetic method of 16ALPHA,17ALPHA-epoxyprogesterone 中国科学院上海有机化学研究所 2017-03-01 — — CN claimed
CN-105543321-A Process for preparing mold oxide through fermentation biosynthesis ZHAO JIANYING 2016-05-04 — — CN claimed
CN-105483028-A Method for synthesizing 11alpha,15alpha-diOH-16alpha,17alpha-epoxyprogesterone through gibberella intermedia CA3-1 UNIV JIANGNAN 2016-04-13 — — CN claimed
CN-105483029-A Method for synthesizing 11alpha,15alpha-diOH-canrenone through gibberella intermedia CA3-1 UNIV JIANGNAN 2016-04-13 — — CN claimed
CN-103113453-B A kind of concentrating under reduced pressure substitutes punching and heats up in a steamer the processing method of producing 16ALPHA,17ALPHA-epoxyprogesterone HUBEI MINSHENG BIOPHARMACEUTICAL CO., LTD. (CN) 2016-03-16 — — CN claimed
CN-104893982-A Rhizopus nigricans and application technology thereof LIJIANG YINGHUA BIOPHARMACEUTICAL CO LTD 2015-09-09 — — CN claimed
CN-103215335-B The method of mold oxide is prepared in mold fermentation biosynthesizing SHANDONG TAIHUA BIO & TECH CO., LTD. (CN) 2015-08-12 — — CN claimed
CN-104610421-A Synthesis method of W-oxide SHANGHAI INST ORGANIC CHEM 2015-05-13 — — CN claimed
CN-103613634-A Recycling method of Oppenauer crude product mother solution SHIYAN HUAKANG CHEMICAL CO LTD 2014-03-05 — — CN claimed
CN-103113453-A Technique for producing 16,17-epoxyprogesterone by vacuum concentration instead of flush distillation HUBEI MINSHENG BIOPHARMACEUTICAL CO LTD 2013-05-22 — — CN claimed
CN-103088013-A Rhizopus nigricans as well as microbial conversion method for catalyzing hydroxylation reaction of steroid of rhizopus nigricans HUNAN KEYUAN BIO PRODUCTS CO LTD 2013-05-08 — — CN claimed
CN-103088099-A Biological fermentation method of mould oxide TIANJIN PACIFIC CHEMICAL & PHARMACEUTICAL CO LTD 2013-05-08 — — CN claimed
EP-4724107-A2 OPHTHALMIC FILMS Fount Bio, Inc. (US) 2026-04-15 — — EP disclosed
WO-2024254278-A9 OPHTHALMIC FILMS FOUNT BIO, INC. (US) 2025-02-13 — — WO disclosed
EP-0034115-B1 PROCESS FOR THE PREPARATION OF 6-METHYLENE STEROIDS SCHERING AKTIENGESELLSCHAFT (DE) 1983-06-08 — — EP disclosed
US-4322349-A Process for preparing 6-methylene steroids SCHERING AKTIENGESELLSCHAFT (DE) 1982-03-30 — — US disclosed
EP-0034115-A2 Process for the preparation of 6-methylene steroids SCHERING AKTIENGESELLSCHAFT (DE) 1981-08-19 — — EP disclosed
Send feedback