SCHEMBL8463244

SCHEMBL8463244

O=C1C[C@H](C(Cl)(Cl)Cl)O1

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
SCHEMBL7406013 1.00
SCHEMBL8673074 1.00
SCHEMBL8587350 0.79
SCHEMBL2877317 0.79
SCHEMBL1115349 0.74 SMN1; SMN2 (0.41)
SCHEMBL9515375 0.72
SCHEMBL8352516 0.72
SCHEMBL6422632 0.67 NR1I2 (0.32)
SCHEMBL10018502 0.67
SCHEMBL10018500 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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-10087547-A None JP disclosed
EP-2595951-B1 A PROCESS FOR THE PRODUCTION OF CARNITINE LONZA AG (CH) 2014-04-16 EP disclosed
US-8563752-B2 Process for the production of carnitine by cycloaddition LONZA LTD. (CH) 2013-10-22 US disclosed
US-20120022275-A1 PROCESS FOR THE PRODUCTION OF CARNITINE BY CYCLOADDITION LONZA LTD. (CH) 2012-01-26 US disclosed
WO-2012010296-A1 A PROCESS FOR THE PRODUCTION OF CARNITINE LONZA LTD (CH) 2012-01-26 WO disclosed
EP-2409965-A1 A process for the production of carnitine by cycloaddition Lonza Ltd. (CH) 2012-01-25 EP disclosed
CN-101486692-B Preparation of optically pure (R)-4-trihalomethyl-2-heterocycle butanone FUDAN UNIVERSITY (CN) 2011-12-07 CN disclosed
CN-101486692-A Preparation of optically pure (R)-4-trihalomethyl-2-heterocycle butanone UNIV FUDAN (CN) 2009-07-22 CN disclosed
US-5977330-A AS HUMECTANTS FOR SKIN AND MUCOUS MEMBRANES; ANTIDEPOSIT AGENTS CIBA SPECIALTY CHEMICALS CORPORATION (US) 1999-11-02 US disclosed
JP-H1087547-A PRODUCTION OF OPTICALLY ACTIVE SYNTHETIC INTERMEDIATE NIPPON SODA CO LTD 1998-04-07 JP disclosed
US-5708152-A DERIVATIVES AS HUMECTANTS AND ANTIDEPOSIT AGENTS CIBA SPECIALTY CHEMICALS CORPORATION (US) 1998-01-13 US disclosed
EP-0375611-B1 ENANTIOMERIC SILANES, MODIFIED SUPPORT AND ITS USE CIBA-GEIGY AG (CH) 1993-04-07 EP disclosed
EP-0376883-B1 ENANTIOMERIC SILANES, MODIFIED SUPPORT AND ITS USE CIBA-GEIGY AG (CH) 1993-04-07 EP disclosed
US-4997966-A Chromatography, chemical condensation CIBA-GEIGY CORPORATION (US) 1991-03-05 US disclosed
US-4997965-A Chromatography CIBA-GEIGY CORPORATION (US) 1991-03-05 US disclosed
EP-0376883-A1 Enantiomeric silanes, modified support and its use CIBA-GEIGY AG (CH) 1990-07-04 EP disclosed
EP-0375611-A1 Enantiomeric silanes, modified support and its use CIBA-GEIGY AG (CH) 1990-06-27 EP disclosed