SCHEMBL981795

SCHEMBL981795

O=C1OCCC1Cl

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
SCHEMBL981115 0.84
SCHEMBL258847 0.82
SCHEMBL18159135 0.82
SCHEMBL874698 0.69
SCHEMBL17845747 0.69
SCHEMBL7077764 0.69
SCHEMBL1457003 0.69
SCHEMBL1262952 0.69
SCHEMBL979504 0.67
SCHEMBL2738310 0.67

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108752283-A A kind of prothioconazoles new technique for synthesizing 江苏澄扬作物科技有限公司 2018-11-06 CN claimed
JP-4786551-B2 2011-10-05 JP claimed
CN-1918094-B Method for producing optically active alcohols or carboxylic acids BASF AG 2010-12-08 CN claimed
CN-1918095-B Hydrogenation method for producing optically active alcohols or carboxylic acids BASF AG 2010-12-08 CN claimed
US-7507866-B2 Decarboxylation/hydroxylation without the release of carbon monoxide by using a mixed-oxide, supported, hydrogenation catalyst based on rhenium oxide with an absense of ruthenium and, in some cases, platinum and palladium; autoclaving malic acid to obtain hydroxybutyrolactone and 1,2,4-butanetriol BASF AG (DE) 2009-03-24 US claimed
EP-1716091-B1 METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOLS OR CARBOXYLIC ACIDS BASF SE (DE) 2009-02-18 EP claimed
US-20070142648-A1 Hydrogenation method for producing optically active alcohols or carboxylic acids BASF AKTIENGESELLSCHAFT (DE) 2007-06-21 US claimed
US-20070135648-A1 Decarboxylation/hydroxylation without the release of carbon monoxide by using a mixed-oxide, supported, hydrogenation catalyst based on rhenium oxide with an absense of ruthenium and, in some cases, platinum and palladium; autoclaving malic acid to obtain hydroxybutyrolactone and 1,2,4-butanetriol BASF AKTIENGESELLSCHAFT (DE) 2007-06-14 US claimed
CN-1918095-A Hydrogenation method for producing optically active alcohols or carboxylic acids BASF AG (DE) 2007-02-21 CN claimed
CN-1918094-A Method for producing optically active alcohols or carboxylic acids BASF AG (DE) 2007-02-21 CN claimed
EP-1716091-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOLS OR CARBOXYLIC ACIDS BASF AKTIENGESELLSCHAFT (DE) 2006-11-02 EP claimed
EP-1716090-A1 HYDROGENATION METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOLS OR CARBOXYLIC ACIDS BASF AKTIENGESELLSCHAFT (DE) 2006-11-02 EP claimed
WO-2005077870-A1 HYDROGENATION METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOLS OR CARBOXYLIC ACIDS BASF AKTIENGESELLSCHAFT (DE) 2005-08-25 WO claimed
WO-2005077871-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOLS OR CARBOXYLIC ACIDS BASF AKTIENGESELLSCHAFT (DE) 2005-08-25 WO claimed
EP-0139234-B1 RESIN COMPOSITION KABUSHIKI KAISHA TOSHIBA (JP) 1989-11-29 EP claimed
US-4599155-A POLYORTHOESTERS;SHRINKAGE INHIBITION;NONCRACKING;COATINGS KABUSHIKI KAISHA TOSHIBA (JP) 1986-07-08 US claimed
EP-0139234-A2 Resin composition KABUSHIKI KAISHA TOSHIBA (JP) 1985-05-02 EP claimed
JP-62216171-A None JP disclosed
EP-0144812-A1 New derivatives of gamma-butyrolactone, method for the preparation thereof and pharmaceutical compositions containing them LABORATORIO FARMACEUTICO CT (IT) 1985-06-19 EP disclosed
EP-0139234-A2 Resin composition KABUSHIKI KAISHA TOSHIBA (JP) 1985-05-02 EP disclosed