SCHEMBL5314742

SCHEMBL5314742

C[C@@](O)(CO)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
SCHEMBL5310436 1.00
SCHEMBL5310441 1.00
SCHEMBL9936963 0.82
SCHEMBL283797 0.78
SCHEMBL6376274 0.75
Ammonia Solution, Strong SCHEMBL888128 0.74
Methyl Alcohol SCHEMBL6345620 0.74
SCHEMBL2678568 0.73
Methylene Chloride SCHEMBL11566778 0.72
SCHEMBL17669231 0.72 ALDH1A1 (0.35)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1550730-B1 Method for producing optically active 3-chloro-2-methyl-1,2-propanediol taking advantage of microorganism DAISO CO LTD (JP) 2007-08-29 EP claimed
US-7235399-B2 Method for producing optically active 3-chloro-2-methyl-1, 2-propanediol taking advantage of microorganism DAISO CO., LTD. (JP) 2007-06-26 US claimed
US-20050153409-A1 Method for producing optically active 3-chloro-2-methyl-1, 2-propanediol taking advantage of microorganism OSAKA SODA CO., LTD. (JP) 2005-07-14 US claimed
EP-1550730-A1 Method for producing optically active 3-chloro-2-methyl-1,2-propanediol taking advantage of microorganism DAISO CO., LTD. (JP) 2005-07-06 EP claimed
EP-1550730-B1 Method for producing optically active 3-chloro-2-methyl-1,2-propanediol taking advantage of microorganism DAISO CO LTD (JP) 2007-08-29 EP disclosed
US-7235399-B2 Method for producing optically active 3-chloro-2-methyl-1, 2-propanediol taking advantage of microorganism DAISO CO., LTD. (JP) 2007-06-26 US disclosed
US-7235399-B2 Method for producing optically active 3-chloro-2-methyl-1, 2-propanediol taking advantage of microorganism DAISO CO., LTD. (JP) 2007-06-26 US disclosed
JP-2006197803-A METHOD FOR PRODUCING OPTICALLY ACTIVE 3-CHLORO-2-METHYL-1,2-PROPANEDIOL USING MICROORGANISM DAISO CO LTD 2006-08-03 JP disclosed
US-20050153409-A1 Method for producing optically active 3-chloro-2-methyl-1, 2-propanediol taking advantage of microorganism OSAKA SODA CO., LTD. (JP) 2005-07-14 US disclosed
US-20050153409-A1 Method for producing optically active 3-chloro-2-methyl-1, 2-propanediol taking advantage of microorganism OSAKA SODA CO., LTD. (JP) 2005-07-14 US disclosed
EP-1550730-A1 Method for producing optically active 3-chloro-2-methyl-1,2-propanediol taking advantage of microorganism DAISO CO., LTD. (JP) 2005-07-06 EP disclosed
EP-1550730-A1 Method for producing optically active 3-chloro-2-methyl-1,2-propanediol taking advantage of microorganism DAISO CO., LTD. (JP) 2005-07-06 EP disclosed
EP-0257503-B1 PROCESS FOR THE PRODUCTION OF OPTICALLY ACTIVE HYDROQUINONE DERIVATIVES AND D-ALPHA-TOCOPHEROL F. HOFFMANN-LA ROCHE AG (CH) 1990-05-23 EP disclosed
US-4808736-A Process for the preparation of hydroquinone derivatives and d-α-tocopherol HOFFMANN-LAROCHE INC. (US) 1989-02-28 US disclosed
EP-0257503-A1 Process for the production of optically active hydroquinone derivatives and d-alpha-tocopherol F. HOFFMANN-LA ROCHE AG (CH) 1988-03-02 EP disclosed