SCHEMBL2382234

SCHEMBL2382234

CCC[C@H](O)CO

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
SCHEMBL62155 1.00
SCHEMBL2381476 1.00
SCHEMBL29157267 1.00 THRB (0.56)
SCHEMBL31303531 0.97
Ammonia Solution, Strong SCHEMBL8212958 0.97
SCHEMBL28231854 0.97
Alcohol SCHEMBL15477222 0.97 THRB (0.53)
Glycerin SCHEMBL3252402 0.97 LMNA (0.56)
Hydrochloric Acid SCHEMBL21682461 0.97
Hydrogen Sulfide SCHEMBL28127902 0.97

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105801518-B A kind of synthetic method of (S) -1-Boc-3- hydroxy piperidine 重庆博腾制药科技股份有限公司 2018-11-27 CN claimed
US-9845303-B2 Process for the preparation of dapagliflozin CADILA HEALTHCARE LIMITED (IN) 2017-12-19 US claimed
US-20170166547-A1 PROCESS FOR THE PREPARATION OF DAPAGLIFLOZIN CADILA HEALTHCARE LIMITED (IN) 2017-06-15 US claimed
CN-105624214-A Bio-preparation of (S)-1,2-pentanediol TIANJIN INST IND BIOTECHNOLOGY CAS 2016-06-01 CN claimed
EP-0317998-B1 Manufacturing method of optically-active 1,2-diols KANEGAFUCHI CHEMICAL IND (JP) 1994-08-31 EP claimed
EP-0300413-B1 MICROBICIDAL AGENTS CIBA-GEIGY AG (CH) 1993-09-01 EP claimed
US-4940799-A Preparation of the diastereomeric mixture 2R,4S-1-[2-(2,4-dichlorophenyl)-4-n-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole CIBA-GEIGY CORPORATION (US) 1990-07-10 US claimed
EP-0317998-A2 Manufacturing method of optically-active 1,2-diols KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1989-05-31 EP claimed
JP-1047783-A None JP disclosed
EP-4103144-B1 COMPOSITIONS COMPRISING UV-FILTERS AND ONE OR MORE (BIO)-ALKANEDIOLS SYMRISE AG (DE) 2026-05-27 EP disclosed
US-20260071146-A1 DISH CLEANING AND/OR DISH RINSING COMPOSITION WITH IMPROVED FINISHING PROPERTIES SYMRISE AG (DE) 2026-03-12 US disclosed
US-20260071145-A1 DETERGENTS AND CLEANING COMPOSITIONS WITH IMPROVED ANTI-REDEPOSITION PROPERTIES SYMRISE AG (DE) 2026-03-12 US disclosed
US-20260071144-A1 DETERGENTS WITH IMPROVED DYE TRANSFER INHIBITION SYMRISE AG (DE) 2026-03-12 US disclosed
US-20260071379-A1 TEXTILE TREATMENT COMPOSITION FOR ANTI-YELLOWING SYMRISE AG (DE) 2026-03-12 US disclosed
WO-2007062308-A2 HOMO- AND HETEROCYCLIC COMPOUNDS SUITABLE AS CETP INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-05-31 WO disclosed
EP-0317998-B1 Manufacturing method of optically-active 1,2-diols KANEGAFUCHI CHEMICAL IND (JP) 1994-08-31 EP disclosed
US-5288747-A Method of controlling or preventing phytopathogenic microorganism infestation of plants using propiconazole as a seed dressing CIBA-GEIGY CORPORATION (US) 1994-02-22 US disclosed
US-4981796-A BIOSYNTHESIS KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1991-01-01 US disclosed
US-4940799-A Preparation of the diastereomeric mixture 2R,4S-1-[2-(2,4-dichlorophenyl)-4-n-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole CIBA-GEIGY CORPORATION (US) 1990-07-10 US disclosed
EP-0317998-A2 Manufacturing method of optically-active 1,2-diols KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1989-05-31 EP disclosed