SCHEMBL2407894

SCHEMBL2407894

COC(=O)CC(O)CC(=O)O

nearest known ligand 0.62

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SLC22A6 Q4U2R8 1/20 0.62
MAPT P10636 1/20 0.46
GABRR1 P24046 2/20 0.46
LMNA P02545 1/20 0.46
TSHR P16473 4/20 0.43
GPR84 Q9NQS5 4/20 0.42
SMN1; SMN2 Q16637 1/20 0.39
HSD17B10 Q99714 1/20 0.39
MGAM O43451 1/20 0.39
GAA P10253 1/20 0.39
SI P14410 1/20 0.39
MGAM2 Q2M2H8 1/20 0.39
TDP1 Q9NUW8 1/20 0.35

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
SCHEMBL2413537 1.00 SLC22A6 (0.62) SLC22A6MAPTGABRR1LMNATSHR
SCHEMBL2414863 1.00 SLC22A6 (0.62) SLC22A6MAPTGABRR1LMNATSHR
SCHEMBL28243 0.90 TSHR (0.50) SLC22A6MAPTLMNATSHRHSD17B10
SCHEMBL15976653 0.81 MGAM (0.50) SLC22A6MAPTLMNATSHRHSD17B10
SCHEMBL13908456 0.81 MGAM (0.50) SLC22A6MAPTLMNATSHRHSD17B10
SCHEMBL12787282 0.81 MGAM (0.50) SLC22A6MAPTLMNATSHRHSD17B10
SCHEMBL5749928 0.80 TSHR (0.48) SLC22A6MAPTGABRR1LMNATSHR
SCHEMBL4744296 0.80 TSHR (0.48) SLC22A6TSHRGPR84
SCHEMBL667017 0.80 TSHR (0.48) SLC22A6TSHRGPR84
SCHEMBL9600868 0.80 SLC22A6 (0.68) SLC22A6MAPTGABRR1LMNATSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106676141-B Enzymatic preparation method of chiral intermediate (S) -3-hydroxy glutaric acid monoester 浙江京新药业股份有限公司 2020-12-08 CN claimed
CN-102798656-B Method for separating 3-hydroxyl glutaric acid monoester enantiomer by high-performance capillary electrophoresis UNIV SHAOXING 2014-06-04 CN claimed
CN-103361386-A Method for preparing rosuvastatin intermediate SUZHOU ENZYMEWORKS INC 2013-10-23 CN claimed
CN-102798656-A Method for separating 3-hydroxyl glutaric acid monoester enantiomer by high-performance capillary electrophoresis UNIV SHAOXING 2012-11-28 CN claimed
WO-2011106546-A1 A PROCESS FOR THE PREPARATION OF ROSUVASTATIN INTERMEDIATE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2011-09-01 WO claimed
CN-101805409-A Polyesterase polymerization process and device PING DONG 2010-08-18 CN claimed
CN-101143824-B Process for preparing 3-hydroxyglutarate compound HENAN YUCHEN FINE CHEMICAL CO LTD 2010-04-21 CN claimed
CN-101143824-A Process for preparing 3-hydroxyglutarate compound HENAN YUCHEN FINE CHEMICAL CO (CN) 2008-03-19 CN claimed
CN-114349633-A Process for the preparation of diesters of glutaconic acid 华烁科技股份有限公司 2022-04-15 CN disclosed
CN-108358783-B 3-substituted glutaric diester and preparation method of glutaconic diester 华烁科技股份有限公司 2021-04-06 CN disclosed
CN-106676141-B Enzymatic preparation method of chiral intermediate (S) -3-hydroxy glutaric acid monoester 浙江京新药业股份有限公司 2020-12-08 CN disclosed
CN-108358783-A 3-substituted glutaric diester and preparation method of glutaconic diester 华烁科技股份有限公司 2018-08-03 CN disclosed
CN-107011378-A The preparation method of high-purity statins drug midbody 南京大学淮安高新技术研究院 2017-08-04 CN disclosed
CN-106676141-A Enzymatic preparation method of chiral intermediate (S)-3-hydroxyglutaric acid monoester 浙江京新药业股份有限公司 2017-05-17 CN disclosed
CN-1163563-C Cyanoacrylate adhesives containing ester and polymer additives �����ɷ� 2004-08-25 CN disclosed
CN-1088084-C Cyanacrylate adhesive HENKEL KGAA (DE) 2002-07-24 CN disclosed
CN-1280602-A Cyanoacrylate adhesives containing ester and polymer additives HENKEL KGAA (DE) 2001-01-17 CN disclosed
CN-1219949-A Cyanacrylate adhesive HENKEL KGAA (DE) 1999-06-16 CN disclosed
CN-1194580-A Ketone derivatives and medical use thereof TORAY INDUSTRIES (JP) 1998-09-30 CN disclosed
US-4992544-A Intermediates for b-lactam antibiotics and b-lactamase inhibitor UNIVERSITY OF NOTRE DAME DU LAC (US) 1991-02-12 US disclosed