SCHEMBL6159440

SCHEMBL6159440

[CH]=CCCCCCl

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
SCHEMBL6156810 0.97 ALDH1A1 (0.38)
SCHEMBL6157837 0.97 ALDH1A1 (0.38)
SCHEMBL6161363 0.97
SCHEMBL6160562 0.97
SCHEMBL11606743 0.97 ALDH1A1 (0.38)
SCHEMBL1006908 0.90
SCHEMBL3499333 0.82
SCHEMBL1541496 0.78
SCHEMBL1025847 0.74
SCHEMBL3498191 0.73

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1267560-C Process for preparing stereoisomer carboxylate BASF AG (DE) 2006-08-02 CN disclosed
EP-1505156-B1 Process for the enantioselective preparation of secondary alcohols by lipase catalysed solvolysis of the corresponding acetoacetic acid ester CONSORTIUM ELEKTROCHEM IND (DE) 2005-12-07 EP disclosed
US-6878672-B2 Herbicidal emulsion compositions TOKUYAMA CORPORATION (JP) 2005-04-12 US disclosed
US-20050032182-A1 Process for the enantioselective preparation of secondary alcohols by lipase-catalyzed solvolysis of the corresponding acetoacetic esters CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH 2005-02-10 US disclosed
EP-1505156-A1 Process for the enantioselective preparation of secondary alcohols by lipase catalysed solvolysis of the corresponding acetoacetic acid ester Consortium für elektrochemische Industrie GmbH (DE) 2005-02-09 EP disclosed
US-20030191024-A1 Herbicidal emulsion compositions TOKUYAMA CORPORATION (JP) 2003-10-09 US disclosed
EP-0901752-B1 Herbicidal composition TOKUYAMA CORP (JP) 2002-11-20 EP disclosed
US-6365398-B1 REACTING RACEMIC CARBOXYLIC ACID ESTER WITH RACEMIC ALCOHOL IN PRESENCE OF A CARBOXYL ESTER HYDROLASE BASF AKTIENGESELLSCHAFT (DE) 2002-04-02 US disclosed
CN-1266904-A Process for preparing stereoisomer carboxylate BASF AG (DE) 2000-09-20 CN disclosed
EP-1031629-A2 Method of preparation of stereoisomeric carboxylic acid esters BASF AKTIENGESELLSCHAFT (DE) 2000-08-30 EP disclosed
US-6083873-A Herbicidal composition TOKUYAMA CORPORATION (JP) 2000-07-04 US disclosed
EP-0774456-B1 Ethenyl amide compounds production process TOKUYAMA CORP (JP) 1999-07-14 EP disclosed
EP-0901752-A1 Herbicidal composition TOKUYAMA CORPORATION (JP) 1999-03-17 EP disclosed
US-5723665-A REACTING SCHIFF BASE WITH ACYL HALIDE UNDER LOW PRESSURE WHILE REMOVING BY-PRODUCED HYDROGEN HALIDE; AMIDATION TOKUYAMA CORPORATION (JP) 1998-03-03 US disclosed
EP-0774456-A1 Ethenyl amide compounds production process TOKUYAMA CORPORATION (JP) 1997-05-21 EP disclosed
EP-0192242-B1 SUBSTITUTED AMINOPHENYLUREA DERIVATIVES TOKUYAMA SODA KABUSHIKI KAISHA (JP) 1990-11-07 EP disclosed
US-4803223-A ANTITUMOR AGENTS TOKUYAMA SODA KABUSHIKI KAISHA (JP) 1989-02-07 US disclosed
EP-0192242-A1 Substituted aminophenylurea derivatives TOKUYAMA SODA KABUSHIKI KAISHA (JP) 1986-08-27 EP disclosed