SCHEMBL7758273

SCHEMBL7758273

COc1cccc(CCCC(=O)O)c1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HDAC1 Q13547 2/20 0.63
▸ HDAC6 Q9UBN7 2/20 0.63
▸ MTNR1A P48039 2/20 0.62
▸ MTNR1B P49286 2/20 0.62
▸ HDAC3 O15379 1/20 0.58
▸ MAPK1 P28482 1/20 0.58
▸ ADRA1A P35348 1/20 0.58
▸ HDAC4 P56524 1/20 0.58
▸ SLC6A3 Q01959 1/20 0.58
▸ SMN1; SMN2 Q16637 1/20 0.58
▸ HDAC7 Q8WUI4 1/20 0.58
▸ HDAC2 Q92769 1/20 0.58
▸ HDAC10 Q969S8 1/20 0.58
▸ HDAC11 Q96DB2 1/20 0.58
▸ HDAC8 Q9BY41 1/20 0.58
▸ HDAC9 Q9UKV0 1/20 0.58
▸ HDAC5 Q9UQL6 1/20 0.58
▸ CYP1A2 P05177 2/20 0.57
▸ CHRM2 P08172 1/20 0.56
▸ CHRM1 P11229 1/20 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
SCHEMBL29669893 1.00 HDAC1 (0.63) HDAC1HDAC6MTNR1AMTNR1BHDAC3
SCHEMBL28188589 0.95 HDAC1 (0.70) HDAC1HDAC6MTNR1AMTNR1BCYP1A2
SCHEMBL1206248 0.95 HDAC1 (0.70) HDAC1HDAC6MTNR1AMTNR1BCYP1A2
SCHEMBL25035334 0.94 HDAC1 (0.72) HDAC1HDAC6MTNR1AMTNR1BCYP1A2
SCHEMBL9663074 0.94 HDAC1 (0.72) HDAC1HDAC6MTNR1AMTNR1BCYP1A2
SCHEMBL710937 0.94 HDAC1 (0.72) HDAC1HDAC6MTNR1AMTNR1BCYP1A2
SCHEMBL17274767 0.94 HDAC1 (0.72) HDAC1HDAC6MTNR1AMTNR1BCYP1A2
SCHEMBL346302 0.90 FFAR1 (0.65) HDAC1HDAC6MTNR1AMTNR1BCYP1A2
SCHEMBL28189252 0.90 PPARA (0.65) HDAC1HDAC6MTNR1AMTNR1B
Heptane SCHEMBL28189233 0.89 PPARA (0.67) HDAC1HDAC6MTNR1AMTNR1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109096417-A A kind of catalyst and olefine polymerizing process for olefinic polymerization 中国石油化工股份有限公司 2018-12-28 — — CN claimed
CN-109096424-A A kind of catalyst and olefine polymerizing process for olefinic polymerization 中国石油化工股份有限公司 2018-12-28 — — CN claimed
CN-109096421-A A kind of catalyst and olefine polymerizing process for olefinic polymerization 中国石油化工股份有限公司 2018-12-28 — — CN claimed
CN-109096418-A A kind of catalyst and olefine polymerizing process for olefinic polymerization 中国石油化工股份有限公司 2018-12-28 — — CN claimed
CN-109096420-A A kind of catalyst and olefine polymerizing process for olefinic polymerization 中国石油化工股份有限公司 2018-12-28 — — CN claimed
US-6289286-B1 Surface regeneration of biosensors and characterization of biomolecules associated therewith BIACORE AB (SE) 2001-09-11 — — US claimed
EP-1082607-A1 SURFACE REGENERATION OF BIOSENSORS Biacore AB (SE) 2001-03-14 — — EP claimed
WO-1999063333-A1 SURFACE REGENERATION OF BIOSENSORS BIACORE AB (SE) 1999-12-09 — — WO claimed
CN-109320458-B Diaryl imidazole-containing compound, preparation method and medical application thereof 中国药科大学 2022-05-31 — — CN disclosed
WO-2021071843-A1 MUSCARINIC ACETYLCHOLINE M1 RECEPTOR ANTAGONISTS Pipeline Therapeutics, Inc. (US) 2021-04-15 — — WO disclosed
CN-109320458-A One kind is containing diarylimidazoles and preparation method thereof and medical usage 中国药科大学 2019-02-12 — — CN disclosed
CN-109096425-A A kind of catalyst and olefine polymerizing process for olefinic polymerization 中国石油化工股份有限公司 2018-12-28 — — CN disclosed
CN-109096419-A A kind of catalyst and olefine polymerizing process for olefinic polymerization 中国石油化工股份有限公司 2018-12-28 — — CN disclosed
EP-2590944-B1 1-PHENYL-SUBSTITUTED HETEROCYCLYL DERIVATIVES AND THEIR USE AS PROSTAGLANDIN D2 RECEPTOR MODULATORS ACTELION PHARMACEUTICALS LTD (CH) 2015-09-30 — — EP disclosed
WO-2007111994-A2 COMPOUNDS AND METHODS FOR TREATMENT OF DISORDERS ASSOCIATED WITH ER STRESS SYNDEXA PHARMACEUTICALS CORPORATION (US) 2007-10-04 — — WO disclosed
US-6289286-B1 Surface regeneration of biosensors and characterization of biomolecules associated therewith BIACORE AB (SE) 2001-09-11 — — US disclosed
EP-1082607-A1 SURFACE REGENERATION OF BIOSENSORS Biacore AB (SE) 2001-03-14 — — EP disclosed
WO-1999063333-A1 SURFACE REGENERATION OF BIOSENSORS BIACORE AB (SE) 1999-12-09 — — WO disclosed
CN-1079648-A Preparation contains the method for the pharmaceutical composition of imidazolyl-alkenoic acids SMITHKLINE BEECHAM CORP (US) 1993-12-22 — — CN disclosed
US-4618683-A Tetrahydro-6,7-dimethoxy-1H-benz[e]isoinodolines useful in the treatment of hypertension and as sedatives ABBOTT LABORATORIES (US) 1986-10-21 — — US disclosed
Send feedback