SCHEMBL2235100

SCHEMBL2235100

CCC=C1OCCO1

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
SCHEMBL2027735 0.72 TSHR (0.36)
SCHEMBL18231554 0.69 ALDH1A1 (0.31)
SCHEMBL27676807 0.69
SCHEMBL24385392 0.67
SCHEMBL2361853 0.67
SCHEMBL6299237 0.66
SCHEMBL2236437 0.65
SCHEMBL9620051 0.65
SCHEMBL8593736 0.64
SCHEMBL29368225 0.63

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102741227-B Aryl benzylamine compounds NOVARTIS AG 2014-07-30 CN claimed
US-8791100-B2 Aryl benzylamine compounds NOVARTIS AG (CH) 2014-07-29 US claimed
EP-2531487-B1 ARYL BENZYLAMINE COMPOUNDS NOVARTIS AG (CH) 2014-06-18 EP claimed
EP-2531487-A1 ARYL BENZYLAMINE COMPOUNDS Novartis AG (CH) 2012-12-12 EP claimed
CN-102741227-A Aryl benzylamine compounds NOVARTIS AG 2012-10-17 CN claimed
WO-2011095452-A1 ARYL BENZYLAMINE COMPOUNDS NOVARTIS AG (CH) 2011-08-11 WO claimed
US-20110190258-A1 ARYL BENZYLAMINE COMPOUNDS NOVARTIS AG (CH) 2011-08-04 US claimed
JP-10139712-A None JP disclosed
CN-102741227-B Aryl benzylamine compounds NOVARTIS AG 2014-07-30 CN disclosed
US-8791100-B2 Aryl benzylamine compounds NOVARTIS AG (CH) 2014-07-29 US disclosed
EP-2531487-B1 ARYL BENZYLAMINE COMPOUNDS NOVARTIS AG (CH) 2014-06-18 EP disclosed
EP-2531487-A1 ARYL BENZYLAMINE COMPOUNDS Novartis AG (CH) 2012-12-12 EP disclosed
CN-102741227-A Aryl benzylamine compounds NOVARTIS AG 2012-10-17 CN disclosed
US-7671231-B2 L-allysine acetal prepared by contacting a 2-butene acetal with a hydroformylation catalyst and synthesis gas to prepare aldehyde mixture; contacting with an enantioselective hydrolase in the presence of water and hydrocyanic acid/ammonia; separation from branched derivatives LLOYD MICHAEL C 2010-03-02 US disclosed
WO-2007084545-A1 PROCESS FOR MAKING AMINO ACIDS DOW GLOBAL TECHNOLOGIES INC. (US) 2007-07-26 WO disclosed
US-20070166806-A1 Process for making amino acids LLOYD MICHAEL C 2007-07-19 US disclosed
US-20070166806-A1 Process for making amino acids LLOYD MICHAEL C 2007-07-19 US disclosed
CN-1133643-C Lactone derivatives of 17-beta-carboxy, carbothio and amide androstane derivatives 2004-01-07 CN disclosed
CN-1209135-A Lactone derivatives of 17-beta-carboxy, carbothio and amide androstane derivatives GLAXO GROUP LTD (GB) 1999-02-24 CN disclosed
JP-H10139712-A PRODUCTION OF NAPHTHYLBUTANONE ARCHIMICA SPA 1998-05-26 JP disclosed