SCHEMBL6882282

SCHEMBL6882282

CCCCCCCCCCCCc1ccc(O)c(C=O)c1

nearest known ligand 0.84

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CDK1 P06493 1/20 0.84
KAT8 Q9H7Z6 2/20 0.59
PPARA Q07869 1/20 0.55
ESR1 P03372 2/20 0.51
ADRA2A P08913 2/20 0.51
ADORA3 P0DMS8 2/20 0.51
TACR2 P21452 2/20 0.51
SLC6A2 P23975 2/20 0.51
SLC6A4 P31645 2/20 0.51
SLC6A3 Q01959 2/20 0.51
KDM4E B2RXH2 1/20 0.51
ALDH1A1 P00352 1/20 0.51
LMNA P02545 1/20 0.51
SHBG P04278 1/20 0.51
TP53 P04637 1/20 0.51
CYP3A4 P08684 1/20 0.51
HSPD1 P10809 1/20 0.51
ADRB3 P13945 1/20 0.51
HTR2C P28335 1/20 0.51
HSPE1 P61604 1/20 0.51

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
SCHEMBL9318508 1.00 CDK1 (0.84) CDK1KAT8PPARAESR1ADRA2A
SCHEMBL11415237 1.00 CDK1 (0.84) CDK1KAT8PPARAESR1ADRA2A
SCHEMBL27840244 1.00 CDK1 (0.84) CDK1KAT8PPARAESR1ADRA2A
SCHEMBL304629 1.00 CDK1 (0.84) CDK1KAT8PPARAESR1ADRA2A
SCHEMBL304974 1.00 CDK1 (0.84) CDK1KAT8PPARAESR1ADRA2A
SCHEMBL304650 1.00 CDK1 (0.84) CDK1KAT8PPARAESR1ADRA2A
SCHEMBL305081 1.00 CDK1 (0.84) CDK1KAT8PPARAESR1ADRA2A
SCHEMBL11421416 1.00 CDK1 (0.84) CDK1KAT8PPARAESR1ADRA2A
SCHEMBL27994247 0.98 CDK1 (0.81) CDK1KAT8PPARAESR1ADRA2A
SCHEMBL305077 0.98 CDK1 (0.81) CDK1KAT8PPARAESR1ADRA2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0631572-B1 OXIMATION PROCESS HENKEL CORP (US) 1998-01-14 EP claimed
EP-0631572-A1 OXIMATION PROCESS HENKEL CORPORATION (US) 1995-01-04 EP claimed
US-5349088-A Reaction of ketone or aldehyde with hydroxylamine in presence of alkylphenol phase transfer catalyst HENKEL CORPORATION (US) 1994-09-20 US claimed
US-5300689-A Using acid phase transfer catalyst HENKEL CORPORATION (US) 1994-04-05 US claimed
WO-1993019041-A1 OXIMATION PROCESS HENKEL CORPORATION (US) 1993-09-30 WO claimed
WO-2014185561-A1 NOVEL COMPOUND OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, AND PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING DISEASES ASSOCIATED WITH UCH-L1, CONTAINING SAME AS ACTIVE INGREDIENT 이화여자대학교 산학협력단 (KR) 2014-11-20 WO disclosed
CN-103572054-A Regeneration process of aldoxime extracting agent in hydrometallurgical extraction system CHONGQING HALLOCHEM PHARMA CO LTD 2014-02-12 CN disclosed
EP-1440130-A1 OXIDATIVELY DRYING COATING COMPOSITION Akzo Nobel Coatings International B.V. (NL) 2004-07-28 EP disclosed
US-20030096893-A1 Can form metal complex having a catalytic effect on the curing of oxidatively drying polymers, in particular alkyd resins AKZO NOBEL N.V. (NL) 2003-05-22 US disclosed
WO-2003029371-A1 OXIDATIVELY DRYING COATING COMPOSITION AKZO NOBEL COATINGS INTERNATIONAL B.V. (NL) 2003-04-10 WO disclosed
US-6288276-B1 CARBONYLATION OF MAGNESIUM SALT OF PHENOL WITH FORMALDEHYDE THEN REACTION WITH AMINE TO FORM OXIME HENKEL KOMMANDITGESELSCHAFT AUF AKTIEN (DE) 2001-09-11 US disclosed
US-6274068-B1 Synthesis of 2-hydroxyarylaldehydes HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN (DE) 2001-08-14 US disclosed
US-5349088-A Reaction of ketone or aldehyde with hydroxylamine in presence of alkylphenol phase transfer catalyst HENKEL CORPORATION (US) 1994-09-20 US disclosed
US-5300689-A Using acid phase transfer catalyst HENKEL CORPORATION (US) 1994-04-05 US disclosed
US-5260487-A Process for the preparation of 2-hydroxyarylaldehydes IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1993-11-09 US disclosed
WO-1993019041-A1 OXIMATION PROCESS HENKEL CORPORATION (US) 1993-09-30 WO disclosed
CN-1073934-A Novel method for synthesizing 2-hydroxy aromatic aldehyde compound ICI PLC (GB) 1993-07-07 CN disclosed
EP-0529870-A2 Preparation of 2-hydroxyarylaldehydes ZENECA LIMITED (GB) 1993-03-03 EP disclosed
US-5100532-A In liquid hydrocarbonaceous media BETZ LABORATORIES, INC. (US) 1992-03-31 US disclosed
US-4200465-A Antistatic light-sensitive silver halide photographic element KONISHIROKU PHOTO INDUSTRY CO., LTD. (JP) 1980-04-29 US disclosed