SCHEMBL202653

SCHEMBL202653

CC(=O)OCC(Cl)CCl

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
SCHEMBL4279785 0.87 TDP1 (0.46)
SCHEMBL1636734 0.82 TDP1 (0.39)
SCHEMBL4279004 0.81
SCHEMBL10835256 0.81
SCHEMBL10836816 0.80 TP53 (0.39)
SCHEMBL10836798 0.79 TP53 (0.35)
SCHEMBL2719789 0.79 TSHR (0.59)
SCHEMBL16860538 0.78 TP53 (0.38)
SCHEMBL11601760 0.78
SCHEMBL29204225 0.78

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4841081-A Method of optically resolving a racemate or a diastereomeric mixture of glycidyl compound OSAKA SODA CO., LTD. (JP) 1989-06-20 US claimed
WO-2024134681-A1 A METHOD FOR THE PREPARATION OF 3-CHLOROTHIETANE 1,1-DIOXIDE PI INDUSTRIES LTD. (IN) 2024-06-27 WO disclosed
EP-2895449-A1 PROCESS OF STRIPPING A LIQUID MEDIUM Solvay SA (BE) 2015-07-22 EP disclosed
EP-2181979-B1 Conversion of a multihydroxylated aliphatic hydrocarbon or ester thereof to a chlorohydrin DOW GLOBAL TECHNOLOGIES LLC (US) 2015-04-22 EP disclosed
EP-2174925-B1 Conversion of a multihydroxylated-aliphatic hydrocarbon or ester thereof to a chlorohydrin DOW GLOBAL TECHNOLOGIES LLC (US) 2014-10-15 EP disclosed
WO-2014040883-A1 PROCESS OF STRIPPING A LIQUID MEDIUM SOLVAY SA (BE) 2014-03-20 WO disclosed
EP-2708525-A1 Process of stripping a liquid medium Solvay SA (BE) 2014-03-19 EP disclosed
US-8404905-B2 Batch, semi-continuous or continuous hydrochlorination of glycerin with reduced volatile chlorinated hydrocarbon by-products and chloroacetone levels DOW GLOBAL TECHNOLOGIES LLC (US) 2013-03-26 US disclosed
US-8404905-B2 Batch, semi-continuous or continuous hydrochlorination of glycerin with reduced volatile chlorinated hydrocarbon by-products and chloroacetone levels DOW GLOBAL TECHNOLOGIES LLC (US) 2013-03-26 US disclosed
US-8404905-B2 Batch, semi-continuous or continuous hydrochlorination of glycerin with reduced volatile chlorinated hydrocarbon by-products and chloroacetone levels DOW GLOBAL TECHNOLOGIES LLC (US) 2013-03-26 US disclosed
US-5177007-A Alcaligenes DAISO CO., LTD. (JP) 1993-01-05 US disclosed
EP-0207636-B1 PROCESS FOR PRODUCING OPTICALLY ACTIVE DICHLOROPROPANOL USING MICROORGANISM Daiso Co., Ltd. (JP) 1992-04-22 EP disclosed
EP-0431970-A2 Process for producing optically active R-(+)-2, 3,-dichloro-1-propanol using microorganism Daiso Co., Ltd. (JP) 1991-06-12 EP disclosed
EP-0220887-B1 METHOD OF OPTICALLY RESOLVING A RACEMATE OR A DIASTEREOMERIC MIXTURE OF GLYCIDYL COMPOUND Daiso Co., Ltd. (JP) 1990-06-27 EP disclosed
US-4841081-A Method of optically resolving a racemate or a diastereomeric mixture of glycidyl compound OSAKA SODA CO., LTD. (JP) 1989-06-20 US disclosed
US-4840907-A CULTIVATING PSEUDOMONAS STRAIN IN MEDIUM WITH RACEMATE OSAKA SODA CO., LTD. (JP) 1989-06-20 US disclosed
EP-0220887-A1 Method of optically resolving a racemate or a diastereomeric mixture of glycidyl compound Daiso Co., Ltd. (JP) 1987-05-06 EP disclosed
EP-0207636-A2 Process for producing optically active dichloropropanol using microorganism Daiso Co., Ltd. (JP) 1987-01-07 EP disclosed
US-4634784-A CHLORINATION OF ALLYL ALCOHOL, DEHYDROCHLORINATION SHOWA DENKO KABUSHIKI KAISHA (JP) 1987-01-06 US disclosed
US-4568759-A Preparation of epoxides THE DOW CHEMICAL COMPANY (US) 1986-02-04 US disclosed