SCHEMBL4827310

SCHEMBL4827310

C=C(C)C=COCC

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
SCHEMBL4827307 1.00
SCHEMBL22011075 0.77
SCHEMBL11814781 0.77 ALDH1A1 (0.30)
SCHEMBL11814776 0.77 ALDH1A1 (0.30)
SCHEMBL10404804 0.77
SCHEMBL10404803 0.77
SCHEMBL29939174 0.77 ATM (0.39)
SCHEMBL15720369 0.75
SCHEMBL6905714 0.75
SCHEMBL11137013 0.75 TSHR (0.41)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2022153867-A1 (METH)ACRYLIC ACID COPOLYMER 株式会社日本触媒 2022-07-21 WO disclosed
CN-101056933-B Amphiphilic block copolymer toughened epoxy resins and electrical laminates made therefrom DOW GLOBAL TECHNOLOGIES INC 2012-11-21 CN disclosed
CN-101864261-B Amphiphilic block copolymer-modified epoxy resin and adhesives made therefrom DOW GLOBAL TECHNOLOGIES INC 2012-09-05 CN disclosed
CN-101772546-B Amphiphilic block copolymers and inorganic nanofillers to enhance thermoset polymer properties DOW GLOBAL TECHNOLOGIES INC 2012-05-23 CN disclosed
CN-101056936-B Amphiphilic block copolymer toughened epoxy resins and powder coatings made therefrom DOW GLOBAL TECHNOLOGIES INC 2012-05-23 CN disclosed
CN-102348757-A Heat curable composition containing a combination of an amphiphilic block copolymer and a polyol and thermoset products thereof DOW GLOBAL TECHNOLOGIES INC 2012-02-08 CN disclosed
CN-102325821-A Curable epoxy resin compositions and cured products therefrom DOW GLOBAL TECHNOLOGIES INC 2012-01-18 CN disclosed
US-7323589-B2 Intermediates for use in retinoid synthesis CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2008-01-29 US disclosed
US-7148372-B2 Intermediates for use in retinoid synthesis CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N.R.S.) (FR) 2006-12-12 US disclosed
US-20060135808-A1 Novel intermediates for use in retinoid synthesis CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N.R.S.) (FR) 2006-06-22 US disclosed
EP-0825168-B1 Preparation of gamma-halotiglinaldehydes HOFFMANN LA ROCHE (CH) 2001-11-21 EP disclosed
US-6018075-A BY REACTING GAMMA-BROMOTIGLIC ALDEHYDE OR GAMMA-CHLOROTIGLIC ALDEHYDE WITH SODIUM OR POTASSIUM ACETATE IN THE PRESENCE OF A PHASE TRANSFER CATALYST AND ORGANIC SOLVENT ROCHE VITAMINS INC. (US) 2000-01-25 US disclosed
US-5990360-A DEETHERIFICATION IN PRESENCE OF AN ALUMINIUM SILICATE CATALYST ROCHE VITAMINS INC. (US) 1999-11-23 US disclosed
US-5786518-A HALOHYDROXYLATION OF ALKOXY-2-METHYL-1,3-BUTADIENE WITH ALKANOL AND HALOGEN THEN HYDROLYSIS ROCHE VITAMINS INC. (US) 1998-07-28 US disclosed
EP-0825168-A2 Preparation of gamma-halotiglinaldehydes F. HOFFMANN-LA ROCHE AG (CH) 1998-02-25 EP disclosed
EP-0806405-A1 Process for the preparation of hexahydrofarnesylacetone from 6,7-dihydrogeraniol and intermediates for their production BASF AKTIENGESELLSCHAFT (DE) 1997-11-12 EP disclosed
US-4474983-A Process for preparing compounds having a 1,5-dimethyl-hexa-1,5-dienylene group by desulphonylation of a corresponding sulphone RHONE-POULENC S.A. (FR) 1984-10-02 US disclosed
US-4433171-A Sulphones having a 1,5-dimethyl-hexa-1,5-dienylene group RHONE-POULENC S.A. (FR) 1984-02-21 US disclosed
US-4331814-A Sulphones having a 1,5-dimethyl-hexa-1,5-dienylene group RHONE POULENC S.A. (FR) 1982-05-25 US disclosed
US-4105697-A Process for the preparation of α, β-ethylenic aldehydes RHONE-POULENC INDUSTRIES (FR) 1978-08-08 US disclosed