SCHEMBL5014725

SCHEMBL5014725

CCOC(=O)CCC(C)C(=O)OCC

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.55
KMT2A Q03164 2/20 0.51
POLB P06746 2/20 0.51
CYP1A2 P05177 1/20 0.47
GAA P10253 2/20 0.46
MGAM O43451 1/20 0.46
SI P14410 1/20 0.46
MGAM2 Q2M2H8 1/20 0.46
ALDH1A1 P00352 5/20 0.43
TRPA1 O75762 1/20 0.43
CYP3A4 P08684 2/20 0.41
CYP2C19 P33261 1/20 0.41
LMNA P02545 1/20 0.41
TSHR P16473 1/20 0.41
CYP4F2 P78329 1/20 0.39
CYP4A11 Q02928 1/20 0.39
HSD17B10 Q99714 2/20 0.39
CHRM1 P11229 1/20 0.39
ALOX15 P16050 1/20 0.39
ADORA1 P30542 1/20 0.39

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
SCHEMBL13572949 1.00 L3MBTL1 (0.55) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL5015129 0.88 L3MBTL1 (0.47) L3MBTL1KMT2APOLBGAAMGAM
SCHEMBL9510213 0.88 CYP1A2 (0.53) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL580291 0.86 CYP1A2 (0.52) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL28250103 0.86 L3MBTL1 (0.46) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL11076712 0.85 CYP1A2 (0.56) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL11076713 0.85 CYP1A2 (0.56) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL11344658 0.85 L3MBTL1 (0.49) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL496560 0.84 KMT2A (0.53) L3MBTL1KMT2APOLBCYP1A2GAA
SCHEMBL494426 0.84 KMT2A (0.53) L3MBTL1KMT2APOLBCYP1A2GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11186660-B2 Internal electron donor compound for preparing α-olefin polymerization catalyst component YINGKOU XIANGYANG CATALYST CO., LTD. 2021-11-30 US claimed
US-20190218317-A1 INTERNAL ELECTRON DONOR COMPOUND FOR PREPARING ALPHA-OLEFIN POLYMERIZATION CATALYST COMPONENT YINGKOU XIANGYANG CATALYST CO LTD (CN) 2019-07-18 US claimed
US-10287371-B2 Internal electron donor compound for preparing α-olefin polymerization catalyst component YINGKOU XIANGYANG CATALYST CO., LTD. (CN) 2019-05-14 US claimed
US-20160229935-A1 Internal Electron Donor Compound for Preparing Alpha-olefin Polymerization Catalyst Component DALIAN UNIVERSITY OF TECHNOLOGY (CN) 2016-08-11 US claimed
US-4168280-A Method for synthesis of 2-hydroxy-3-methyl cyclopent-2-ene-1-one EL PASO PRODUCTS COMPANY (US) 1979-09-18 US claimed
CN-122037004-A Catalyst component for olefin polymerization, catalyst, application of catalyst and olefin polymerization method 中国石油化工股份有限公司 2026-05-15 CN disclosed
CN-108699032-B Polycyclic TLR7/8 antagonists and their use in the treatment of immune disorders 默克专利有限公司 2022-07-22 CN disclosed
US-11186660-B2 Internal electron donor compound for preparing α-olefin polymerization catalyst component YINGKOU XIANGYANG CATALYST CO., LTD. 2021-11-30 US disclosed
CN-113603675-A Polycyclic TLR7/8 antagonists and their use in the treatment of immune disorders 默克专利有限公司 2021-11-05 CN disclosed
US-20190218317-A1 INTERNAL ELECTRON DONOR COMPOUND FOR PREPARING ALPHA-OLEFIN POLYMERIZATION CATALYST COMPONENT YINGKOU XIANGYANG CATALYST CO LTD (CN) 2019-07-18 US disclosed
US-10287371-B2 Internal electron donor compound for preparing α-olefin polymerization catalyst component YINGKOU XIANGYANG CATALYST CO., LTD. (CN) 2019-05-14 US disclosed
US-9850194-B2 Process for double carbonylation of allyl alcohols to corresponding diesters EVONIK DEGUSSA GMBH (DE) 2017-12-26 US disclosed
EP-0338427-B1 PROCESS FOR THE PREPARATION OF ESTERS OLEFINIC UNSATURATED CARBOXYLIC ACIDS WITH A TERMINAL ESTER GROUP BASF Aktiengesellschaft (DE) 1993-08-18 EP disclosed
EP-0338427-A2 Process for the preparation of esters olefinic unsaturated carboxylic acids with a terminal ester group BASF Aktiengesellschaft (DE) 1989-10-25 EP disclosed
EP-0071908-B1 1-, AND 1,1-DISUBSTITUTED-6-SUBSTITUTED-2-CARBAMIMIDOYL-1-CARBADETHIAPEN-2-EM-3-CARBOXYLIC ACIDS, A PROCESS FOR PREPARING AND AN ANTIBIOTIC COMPOSITION CONTAINING THE SAME MERCK & CO. INC. (US) 1989-09-27 EP disclosed
EP-0113101-A1 6-(1-Hydroxyethyl)-2-SR8-1-methyl-1-carbadethiapen-2-em-3-carboxylic acid esters MERCK & CO. INC. (US) 1984-07-11 EP disclosed
US-4454333-A DISTILLATION WITH QUATERNARY PHOSPHONIUM, ARSONIUM OR AMMONIUM RHONE-POULENC CHIMIE DE BASE (FR) 1984-06-12 US disclosed
US-4357141-A FATTY ACID, BENZYL ALCOHOL, CATIONIC POLYMER L'OREAL (FR) 1982-11-02 US disclosed
US-4332966-A N-HETEROCYCLE SOLVENT FOR REACTION OF BUTADIENE, CARBON MONOXIDE AND AH ALCOHOL MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1982-06-01 US disclosed
US-4168280-A Method for synthesis of 2-hydroxy-3-methyl cyclopent-2-ene-1-one EL PASO PRODUCTS COMPANY (US) 1979-09-18 US disclosed