SCHEMBL6238627

SCHEMBL6238627

CCC1C(C)=Cc2ccccc21

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 3/20 0.41
KDM4E B2RXH2 2/20 0.37
LMNA P02545 2/20 0.37
TP53 P04637 1/20 0.37
CHRM2 P08172 1/20 0.37
CYP3A4 P08684 1/20 0.37
CYP2D6 P10635 1/20 0.37
CHRM1 P11229 1/20 0.37
DRD2 P14416 1/20 0.37
ADRA2B P18089 1/20 0.37
ADRA2C P18825 1/20 0.37
NFKB1 P19838 1/20 0.37
CHRM3 P20309 1/20 0.37
SLC6A2 P23975 1/20 0.37
HTR2C P28335 1/20 0.37
ADRA1A P35348 1/20 0.37
HRH1 P35367 1/20 0.37
DRD3 P35462 1/20 0.37
THPO P40225 1/20 0.37
OPRK1 P41145 1/20 0.37

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
SCHEMBL1452870 0.85 HTR2A (0.42) HTR2AKDM4ELMNATP53CHRM2
SCHEMBL1453437 0.85 HTR2A (0.42) HTR2AKDM4ELMNATP53CHRM2
SCHEMBL7783135 0.84 HTR2A (0.39) HTR2AKDM4ELMNATP53CHRM2
SCHEMBL4005225 0.83 HTR2A (0.41) HTR2AKDM4ELMNATP53CHRM2
SCHEMBL28735635 0.82 HTR2A (0.37) HTR2AKDM4ELMNATP53CHRM2
SCHEMBL7105374 0.82 HTR2A (0.47) HTR2AKDM4ELMNATP53CHRM2
SCHEMBL8679551 0.82 HTR2A (0.39) HTR2AKDM4ELMNATP53CHRM2
SCHEMBL1241035 0.80 HTR2A (0.38) HTR2AKDM4ELMNATP53CHRM2
SCHEMBL9455741 0.80 MEN1 (0.33) KDM4EMEN1KMT2AALDH1A1TDP1
SCHEMBL4006186 0.79 HTR2A (0.37) HTR2AKDM4ELMNATP53CHRM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1546078-A1 PROCESS FOR PREPARING ARYL ALLYL ETHERS Dow Global Technologies Inc. (US) 2005-06-29 EP disclosed
US-6838409-B1 Catalyst for olefin/styrene copolymerization, and process for producing olefin/styrene copolymer IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2005-01-04 US disclosed
US-6825294-B1 TRANSITION METAL COMPLEX COMPRISING OXYGEN-CONTAINING AND CARBONYL COMPOUNDS; AND ALKYLATING AGENT; SYNDIOTACTIC ADDITION POLMERIZATION IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2004-11-30 US disclosed
WO-2004013076-A1 PROCESS FOR PREPARING ARYL ALLYL ETHERS DOW GLOBAL TECHNOLOGIES INC. (US) 2004-02-12 WO disclosed
CN-1119305-C Method of making 2,6-dimethylnaphthalene from other dimethylnaphthalene isomers and from dimethyltetralins/dimethyldecalins with methyl group on each ring CHEVRON CHEM CO (US) 2003-08-27 CN disclosed
US-6562918-B1 A catalyst for olefin polymerization, which is obtained by contacting (A) a compound of a transition metal of Groups 4 to 6 of the Periodic Table, (B) an organoaluminiumoxy compound, and optionally (C) a carrier with each other, and for which IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2003-05-13 US disclosed
US-6486272-B1 METAL COMPOUND INTERACTS WITH A VINYL COMPOUND WITH A FUNCTIONAL GROUP TO MASK IT AND COPOLYMERIZING WITH A STYRENE IN THE PRESENCE OF TRANSITION METAL COMPOUND, OXYGEN COMPOUNDS WHICH FORM IONIC COMPLEXES, AND AN ORGANOMETALLIC COMPOUND IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2002-11-26 US disclosed
US-20020173605-A1 PROCESS FOR PRODUCING FUNCTIONAL STYRENE COPOLYMER AND FUNCTIONAL STYRENE COPOLYMER IDEMITSU KOSAN CO.,LTD. (JP) 2002-11-21 US disclosed
EP-0996608-B1 METHOD OF MAKING 2,6-DIMETHYLNAPHTHALENE FROM OTHER DIMETHYLNAPHTHALENE ISOMERS AND FROM DIMETHYLTETRALINS/DIMETHYLDECALINS WITH A METHYL GROUP ON EACH RING CHEVRON PHILLIPS CHEMICAL CO (US) 2002-07-03 EP disclosed
EP-1219649-A1 PROCESS FOR PRODUCING FUNCTIONAL STYRENE COPOLYMER AND FUNCTIONAL STYRENE COPOLYMER IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2002-07-03 EP disclosed
EP-1167394-A1 CATALYST FOR OLEFIN/STYRENE COPOLYMERIZATION AND PROCESS FOR PRODUCING OLEFIN/STYRENE COPOLYMER IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2002-01-02 EP disclosed
CN-1303382-A Epoxidation process for aryl allyl ethers DOW CHEMICAL CO (US) 2001-07-11 CN disclosed
US-6255244-B1 OBTAINED BY CONTACTING A TRANSITION METAL COMPOUND, AN OXYGEN-CONTAINING COMPOUND TO FORM AN IONIC COMPLEX, AND AN ADSORBING SUBSTANCE DURING OR AFTER THE CONTACTING TREATMENT, THEN FOLLOWED BY REMOVING THE ADSORBING SUBSTANCE. IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2001-07-03 US disclosed
EP-1085025-A1 CATALYST FOR OLEFIN POLYMERIZATION, PROCESS FOR PRODUCING THE SAME, AND PROCESS FOR PRODUCING OLEFIN POLYMER Idemitsu Petrochemical Co., Ltd. (JP) 2001-03-21 EP disclosed
EP-1085026-A1 CATALYST FOR POLYMERIZING STYRENE AND OTHER MONOMER AND PROCESS FOR PRODUCING STYRENE POLYMER IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2001-03-21 EP disclosed
CN-1263518-A Method of making 2,6-dimethylnaphthalene from other dimethylnaphthalene isomers and from dimethyltetralins/dimethyldecalins with methyl group on each ring CHEVRON CHEM CO (US) 2000-08-16 CN disclosed
EP-0996608-A1 METHOD OF MAKING 2,6-DIMETHYLNAPHTHALENE FROM OTHER DIMETHYLNAPHTHALENE ISOMERS AND FROM DIMETHYLTETRALINS/DIMETHYLDECALINS WITH A METHYL GROUP ON EACH RING Chevron Chemical Company LLC (US) 2000-05-03 EP disclosed
US-6015930-A HYDROISOMERIZING WITH ACIDIC CATALYST AND METAL, DEHYDROGENATING WITH REFORMING CATALYST CHEVRON CHEMICAL COMPANY (US) 2000-01-18 US disclosed
EP-0945458-A2 Transition metal compound, polymerization catalyst comprising it, and method for producing polymers using the polymerization catalyst IDEMITSU PETROCHEMICAL CO., LTD. (JP) 1999-09-29 EP disclosed
WO-1999003805-A1 METHOD OF MAKING 2,6-DIMETHYLNAPHTHALENE FROM OTHER DIMETHYLNAPHTHALENE ISOMERS AND FROM DIMETHYLTETRALINS/DIMETHYLDECALINS WITH A METHYL GROUP ON EACH RING CHEVRON CHEMICAL COMPANY LLC (US) 1999-01-28 WO disclosed