SCHEMBL514908

SCHEMBL514908

C=CCCCCCC(=O)OCCC

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.62
LMNA P02545 2/20 0.62
TSHR P16473 3/20 0.59
DGKA P23743 2/20 0.58
MAPT P10636 3/20 0.50
ABCC4 O15439 1/20 0.50
DNM1 Q05193 1/20 0.49
MGLL Q99685 1/20 0.46
THRB P10828 1/20 0.45
CNR1 P21554 1/20 0.45
CYP3A4 P08684 2/20 0.45
ALOX15 P16050 1/20 0.45
HSD17B10 Q99714 1/20 0.45
TDP1 Q9NUW8 1/20 0.45
PAM P19021 2/20 0.44
USP2 O75604 1/20 0.43
RECQL P46063 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
PRSS1 P07477 1/20 0.43
PRSS2 P07478 1/20 0.43

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
SCHEMBL15758052 1.00 ALDH1A1 (0.62) ALDH1A1LMNATSHRDGKAMAPT
SCHEMBL3694489 1.00 ALDH1A1 (0.62) ALDH1A1LMNATSHRDGKAMAPT
SCHEMBL514724 1.00 ALDH1A1 (0.62) ALDH1A1LMNATSHRDGKAMAPT
SCHEMBL6434039 1.00 ALDH1A1 (0.62) ALDH1A1LMNATSHRDGKAMAPT
SCHEMBL515243 0.98 ALDH1A1 (0.59) ALDH1A1LMNATSHRDGKAMAPT
SCHEMBL514827 0.93 TSHR (0.53) ALDH1A1LMNATSHRDGKAMAPT
SCHEMBL14763919 0.91 TSHR (0.62) ALDH1A1LMNATSHRDGKAMAPT
SCHEMBL3111539 0.91 TSHR (0.62) ALDH1A1LMNATSHRDGKAMAPT
SCHEMBL515244 0.91 TSHR (0.62) ALDH1A1LMNATSHRDGKAMAPT
SCHEMBL514084 0.91 TSHR (0.62) ALDH1A1LMNATSHRDGKAMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4950798-A CHELATE COMPOUNDS AS CATALYSTS UNIVERSITY OF VICTORIA (CA) 1990-08-21 US claimed
EP-4508056-A1 INDOLE-FUNCTIONALIZED BISPHOSPHORAMIDITES, METHODS FOR THE PREPARATION THEREOF, AND RHODIUM-LIGAND COMPLEX Dow Global Technologies LLC (US) 2025-02-19 EP disclosed
CN-118946574-A Indole-functionalized biphosphinamides, method for the production thereof and rhodium-ligand complexes 陶氏环球技术有限责任公司 2024-11-12 CN disclosed
WO-2023200935-A1 INDOLE-FUNCTIONALIZED BISPHOSPHORAMIDITES, METHODS FOR THE PREPARATION THEREOF, AND RHODIUM-LIGAND COMPLEX DOW GLOBAL TECHNOLOGIES LLC (US) 2023-10-19 WO disclosed
CN-116529231-A Hydroformylation process 陶氏技术投资有限责任公司 2023-08-01 CN disclosed
CN-110709374-A Hydroformylation process 陶氏技术投资有限责任公司 2020-01-17 CN disclosed
CN-104955568-A Process for stabilizing a phosphite ligand against degradation DOW TECHNOLOGY INVESTMENTS LLC 2015-09-30 CN disclosed
CN-104379258-A Hydroformylation process DOW TECHNOLOGY INVESTMENTS LLC 2015-02-25 CN disclosed
EP-2415740-B1 METHOD FOR PRODUCING HIGH-PURITY TERMINAL OLEFIN COMPOUND KURARAY CO (JP) 2013-12-25 EP disclosed
US-8609886-B2 Method for producing high purity terminal olefin compound KURARAY CO., LTD. (JP) 2013-12-17 US disclosed
EP-0096986-A2 Hydroformylation process DAVY McKEE (LONDON) LIMITED (GB) 1983-12-28 EP disclosed
EP-0096987-A2 Hydroformylation process DAVY McKEE (LONDON) LIMITED (GB) 1983-12-28 EP disclosed
EP-0073398-A1 Hydroformylation process using a rhodium complex catalyst with triarylphosphine and biphosphine monoxide ligands UNION CARBIDE CORPORATION (US) 1983-03-09 EP disclosed
US-4348539-A Heteronuclear-bridged rhodium clusters UNION CARBIDE CORPORATION (US) 1982-09-07 US disclosed
EP-0018393-B1 PROCESS FOR THE PRODUCTION OF OXYGENATED PRODUCTS FROM OLEFINICALLY UNSATURATED COMPOUNDS BY HYDROFORMYLATION WITH SUPPRESSION OF OLEFIN HYDROGENATION GENERAL ELECTRIC COMPANY (US) 1982-06-23 EP disclosed
US-4288380-A Heteronuclear-bridged rhodium clusters UNION CARBIDE CORPORATION (US) 1981-09-08 US disclosed
US-4224255-A Process for the production of aldehydes and alcohols from olefinically unsaturated compounds by hydroformylation with suppression of olefin hydrogenation GENERAL ELECTRIC COMPANY (US) 1980-09-23 US disclosed
US-4052461-A ALDEHYDES FROM OLEFINS, CARBON MONOXIDE AND HYDROGEN, RHODIUM CATALYST MONSANTO COMPANY (US) 1977-10-04 US disclosed
US-3946082-A ALDEHYDES, CARBON MONOXIDE, HYDROGEN EXXON RESEARCH & ENGINEERING CO. (US) 1976-03-23 US disclosed
US-3939188-A Preparation of zerovalent phosphine substituted rhodium compounds and their use in the selective carbonylation of olefins EXXON RESEARCH AND ENGINEERING COMPANY (US) 1976-02-17 US disclosed