SCHEMBL4020219

SCHEMBL4020219

CC1(C)OC(=O)OC1=O

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
SCHEMBL7637933 0.80
SCHEMBL820849 0.74 LMNA (0.32)
SCHEMBL599372 0.74 LMNA (0.39)
SCHEMBL23214498 0.72
SCHEMBL47839 0.72
SCHEMBL18287705 0.72
SCHEMBL16768797 0.69 TSHR (0.38)
SCHEMBL28945704 0.69 LMNA (0.36)
SCHEMBL7042707 0.69 ALDH1A1 (0.31)
SCHEMBL18287715 0.69

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
EP-3113274-B1 NON-AQUEOUS ELECTROLYTIC SOLUTION AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY USING SAME MITSUBISHI CHEM CORP (JP) 2020-09-30 EP disclosed
EP-3113274-A1 NONAQUEOUS ELECTROLYTE SOLUTION AND NONAQUEOUS-ELECTROLYTE-SOLUTION SECONDARY BATTERY USING SAME Mitsubishi Chemical Corporation (JP) 2017-01-04 EP disclosed
US-20160359197-A1 NON-AQUEOUS ELECTROLYTIC SOLUTION AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY USING THE SAME MITSUBISHI CHEMICAL CORPORATION (JP) 2016-12-08 US disclosed
US-20160359197-A1 NON-AQUEOUS ELECTROLYTIC SOLUTION AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY USING THE SAME MITSUBISHI CHEMICAL CORPORATION (JP) 2016-12-08 US disclosed
US-20140343039-A1 PROCESS FOR PREPARING CEPHALOTAXINE ESTERS ROBIN JEAN-PIERRE (CH) 2014-11-20 US disclosed
US-20140343039-A1 PROCESS FOR PREPARING CEPHALOTAXINE ESTERS ROBIN JEAN-PIERRE (CH) 2014-11-20 US disclosed
EP-1817359-B1 METHOD FOR CONTROLLED POLYMERIZATION OF O-CARBOXY ANHYDRIDES DERIVED FROM ALPHA-HYDROXY ACIDS CENTRE NAT RECH SCIENT (FR) 2013-05-22 EP disclosed
EP-1817359-B1 METHOD FOR CONTROLLED POLYMERIZATION OF O-CARBOXY ANHYDRIDES DERIVED FROM ALPHA-HYDROXY ACIDS CENTRE NAT RECH SCIENT (FR) 2013-05-22 EP disclosed
US-20120022250-A1 PROCESS FOR PREPARING CEPHALOTAXINE ESTERS ROBIN JEAN-PIERRE (CH) 2012-01-26 US disclosed
US-20120022250-A1 PROCESS FOR PREPARING CEPHALOTAXINE ESTERS ROBIN JEAN-PIERRE (CH) 2012-01-26 US disclosed
WO-2010103405-A2 PROCESS FOR PREPARING CEPHALOTAXINE ESTERS ROBIN JEAN-PIERRE (CH) 2010-09-16 WO disclosed
US-7528211-B2 Method for controlled polymerization of o-carboxy anhydrides derived from α-hydroxy acids ISOCHEM (FR) 2009-05-05 US disclosed
US-7528211-B2 Method for controlled polymerization of o-carboxy anhydrides derived from α-hydroxy acids ISOCHEM (FR) 2009-05-05 US disclosed
US-7528211-B2 Method for controlled polymerization of o-carboxy anhydrides derived from α-hydroxy acids ISOCHEM (FR) 2009-05-05 US disclosed
US-20070249654-A1 Method for controlled polymerization of o-carboxy anhydrides derived from alpha-hydroxy acids ISOCHEM 2007-10-25 US disclosed
US-20070249654-A1 Method for controlled polymerization of o-carboxy anhydrides derived from alpha-hydroxy acids ISOCHEM 2007-10-25 US disclosed
US-20070249654-A1 Method for controlled polymerization of o-carboxy anhydrides derived from alpha-hydroxy acids ISOCHEM 2007-10-25 US disclosed
EP-1817359-A1 METHOD FOR CONTROLLED POLYMERIZATION OF O-CARBOXY ANHYDRIDES DERIVED FROM ALPHA-HYDROXY ACIDS ISOCHEM (FR) 2007-08-15 EP disclosed
WO-2006037812-A1 METHOD FOR CONTROLLED POLYMERIZATION OF O-CARBOXY ANHYDRIDES DERIVED FROM ALPHA-HYDROXY ACIDS ISOCHEM (FR) 2006-04-13 WO disclosed