SCHEMBL7060645

SCHEMBL7060645

C/C(Cl)=C/CO

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
SCHEMBL7060646 1.00
SCHEMBL12546991 1.00
SCHEMBL3863230 0.71
SCHEMBL2076271 0.71
SCHEMBL501200 0.71
SCHEMBL501201 0.71
SCHEMBL2076270 0.71
SCHEMBL12423858 0.71
SCHEMBL4205700 0.69
SCHEMBL8813968 0.69 KMT2A (0.55)

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 19 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6608232-B1 Acylating an aromatic compound in presence of zeolite or friedel crafts catalyst, reduction to a carbinol and cata-lytic etherification Chimie, Rhodia (FR) 2003-08-19 US claimed
EP-0994838-B1 METHOD FOR ETHERIFYING A BENZYL ALCOHOL, RESULTING PRODUCTS AND APPLICATIONS RHODIA CHIMIE SA (FR) 2003-05-21 EP claimed
US-6362378-B1 REACTION WITH AN ALCOHOL; ZEOLITE CATALYST; PERFUMES RHODIA CHIMIE (FR) 2002-03-26 US claimed
EP-1140758-A1 METHOD FOR PREPARING A BENZYLIC-TYPE ETHER RHODIA CHIMIE (FR) 2001-10-10 EP claimed
WO-2000040535-A1 METHOD FOR PREPARING A BENZYLIC-TYPE ETHER RHODIA CHIMIE (FR) 2000-07-13 WO claimed
EP-0994838-A1 METHOD FOR ETHERIFYING A BENZYL ALCOHOL, RESULTING PRODUCTS AND APPLICATIONS RHODIA CHIMIE (FR) 2000-04-26 EP claimed
WO-1999002475-A1 METHOD FOR ETHERIFYING A BENZYL ALCOHOL, RESULTING PRODUCTS AND APPLICATIONS RHODIA CHIMIE (FR) 1999-01-21 WO claimed
WO-2023006699-A1 CELLS AND METHOD FOR PRODUCING ISOPRENOID MOLECULES WITH CANONICAL AND NON-CANONICAL STRUCTURES Københavns Universitet (DK) 2023-02-02 WO disclosed
US-6608232-B1 Acylating an aromatic compound in presence of zeolite or friedel crafts catalyst, reduction to a carbinol and cata-lytic etherification Chimie, Rhodia (FR) 2003-08-19 US disclosed
EP-0994838-B1 METHOD FOR ETHERIFYING A BENZYL ALCOHOL, RESULTING PRODUCTS AND APPLICATIONS RHODIA CHIMIE SA (FR) 2003-05-21 EP disclosed
JP-2003040819-A METHOD FOR PRODUCING ACETYLENE ALCOHOL DENKI KAGAKU KOGYO KK 2003-02-13 JP disclosed
US-6362378-B1 REACTION WITH AN ALCOHOL; ZEOLITE CATALYST; PERFUMES RHODIA CHIMIE (FR) 2002-03-26 US disclosed
EP-1140758-A1 METHOD FOR PREPARING A BENZYLIC-TYPE ETHER RHODIA CHIMIE (FR) 2001-10-10 EP disclosed
WO-2000040535-A1 METHOD FOR PREPARING A BENZYLIC-TYPE ETHER RHODIA CHIMIE (FR) 2000-07-13 WO disclosed
EP-0994838-A1 METHOD FOR ETHERIFYING A BENZYL ALCOHOL, RESULTING PRODUCTS AND APPLICATIONS RHODIA CHIMIE (FR) 2000-04-26 EP disclosed
WO-1999002475-A1 METHOD FOR ETHERIFYING A BENZYL ALCOHOL, RESULTING PRODUCTS AND APPLICATIONS RHODIA CHIMIE (FR) 1999-01-21 WO disclosed
EP-0084856-B2 5,6,7-Trinor-4, 8-inter-m-phenylene prostaglandin I2 derivatives TORAY INDUSTRIES (JP) 1994-05-04 EP disclosed
EP-0084856-B1 5,6,7-TRINOR-4, 8-INTER-M-PHENYLENE PROSTAGLANDIN I2 DERIVATIVES TORAY INDUSTRIES, INC. (JP) 1986-11-20 EP disclosed
US-4474802-A 5,6,7-Trinor-4,8-inter-m-phenylene prostaglandin I2 derivatives useful in anti-ulcer, hypotensive and platelet aggregation inhibiting compositions TORAY INDUSTRIES, INC. (JP) 1984-10-02 US disclosed