SCHEMBL295955

SCHEMBL295955

CC(C)=CC=C(Br)Br

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL11751737 0.78
SCHEMBL134414 0.78
SCHEMBL24179615 0.77
SCHEMBL18513525 0.75
SCHEMBL299625 0.72
SCHEMBL299626 0.72
SCHEMBL14616070 0.67
SCHEMBL19027920 0.67
SCHEMBL21737188 0.67
SCHEMBL14654856 0.65 TSHR (0.38)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6011169-A Process for producing optically active cyclopropanecaboxylic acid esters SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2000-01-04 US claimed
US-4328363-A Manufacture of gamma halogen substituted adducts MOBIL OIL CORPORATION (US) 1982-05-04 US claimed
EP-1783111-B1 METHOD FOR PRODUCING OPTICALLY ACTIVE CYCLOPROPANECARBOXYLATE COMPOUND SUMITOMO CHEMICAL CO (JP) 2015-04-08 EP disclosed
EP-2781522-A1 OPTICALLY ACTIVE BISOXAZOLINE COMPOUND, ASYMMETRIC CATALYST, AND METHOD FOR PRODUCING OPTICALLY ACTIVE CYCLOPROPANE COMPOUND USING SAID CATALYST Sumitomo Chemical Company, Limited (JP) 2014-09-24 EP disclosed
EP-1607136-B1 OPTICALLY ACTIVE COPPER CATALYST COMPOSITION SUMITOMO CHEMICAL CO (JP) 2012-05-23 EP disclosed
EP-1683783-B1 Chiral copper complex and production processes thereof and using the same SUMITOMO CHEMICAL CO (JP) 2012-03-14 EP disclosed
EP-1683782-B1 Chiral copper complex and production processes thereof and using the same SUMITOMO CHEMICAL CO (JP) 2012-03-14 EP disclosed
EP-1593674-B1 OPTICALLY ACTIVE BISOXAZOLINE COMPOUNDS, PROCESS FOR PRODUCTION OF THE SAME AND USE THEREOF SUMITOMO CHEMICAL CO (JP) 2011-07-20 EP disclosed
EP-1253135-B1 Asymmetric copper complex and cyclopropanation reaction using the same SUMITOMO CHEMICAL CO (JP) 2010-11-24 EP disclosed
US-7709651-B2 asymmetriccomplex of copper(I) trifluoromethanesulfonate and 1,1-bis[2-[(4S)-(tert-butyl)-oxazoline]]cyclopropane is added to 3-methyl-2-butenyl acetate and ethyl diazoacetate using dichloroethane solvent to effect reaction to produce ethyl 3,3-dimethyl-2-(acetoxymethyl)cyclopropanecarboxylate SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-05-04 US disclosed
US-7705165-B2 Method for producing optically active cyclopropanecarboxylate compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-04-27 US disclosed
EP-0007154-B1 PROCESS FOR THE PREPARATION OF CYCLOPROPANE DERIVATIVES, INTERMEDIATES IN THE SYNTHESIS OF PYRETHROID INSECTICIDES IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1981-12-30 EP disclosed
US-4284582-A REACTING A HALOGENATED DIENE WITH A CYANIDE COMPOUND IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1981-08-18 US disclosed
EP-0022972-A1 Menthyl esters, process for their preparation and their use in enantiomer separation of chiral carboxylic acids BAYER AG (DE) 1981-01-28 EP disclosed
EP-0002477-B1 PROCESS FOR PREPARING 1,1-DIHALO-4-METHYL-1,3-PENTADIENES BAYER AG (DE) 1980-08-06 EP disclosed
US-4191712-A Process for the preparation of 1,1-dihalo-4-methyl-1,3-pentadiene compounds BAYER AKTIENGESELLSCHAFT (DE) 1980-03-04 US disclosed
EP-0007154-A1 Process for the preparation of cyclopropane derivatives, intermediates in the synthesis of pyrethroid insecticides IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1980-01-23 EP disclosed
EP-0002477-A1 Process for preparing 1,1-dihalo-4-methyl-1,3-pentadienes BAYER AG (DE) 1979-06-27 EP disclosed
US-4098657-A Electrolyte dehydrohalogenation of α-haloalcohols IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1978-07-04 US disclosed
US-4022672-A Electrochemical synthesis of insecticide intermediates FMC CORPORATION (US) 1977-05-10 US disclosed