SCHEMBL4653435

SCHEMBL4653435

C[C@]1(O)C(=O)OC[C@H]1O

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
SCHEMBL14566659 1.00
SCHEMBL7262112 1.00
SCHEMBL5301166 1.00
SCHEMBL1824543 0.80 TP53 (0.33)
SCHEMBL5305197 0.80 TP53 (0.33)
SCHEMBL10046442 0.79
SCHEMBL7758201 0.78 LMNA (0.35)
SCHEMBL8846091 0.77
SCHEMBL2879499 0.76
SCHEMBL16481012 0.76

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2007025304-A2 PROCESS FOR PREPARING SACCHARINIC ACIDS AND LACTONES THE CHANCELLORS, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD (GB) 2007-03-01 WO claimed
WO-2005030786-A1 3'-N-SUBSTITUTED-3-O-SUBSTITUTED ERYTHRONOLIDE A DERIVATIVES RANBAXY LABORATORIES LIMITED (US) 2005-04-07 WO claimed
US-11304927-B2 Bioactive extract, fraction of Cassia occidentalis and formulation thereof for bone regeneration COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2022-04-19 US disclosed
CN-107207418-A 4-azidobutylamine and preparation method thereof 森普拉制药公司 2017-09-26 CN disclosed
EP-2319853-B1 Process for the production of 2'-branched nucleosides IDENIX PHARMACEUTICALS INC (US) 2014-03-12 EP disclosed
CN-103619849-A Process for preparation of ketolide intermediates WOCKHARDT LTD 2014-03-05 CN disclosed
EP-1602354-B1 Use of polyglutamic acid or its salts MEIJI SEIKA KAISHA (JP) 2008-11-05 EP disclosed
EP-1604647-B1 Cosmetic composition containing polyorganosiloxane-containing epsilon-polylysine polymer, and polyhydric alcohol, and production thereof CHISSO CORP (JP) 2008-05-07 EP disclosed
WO-2007025304-A2 PROCESS FOR PREPARING SACCHARINIC ACIDS AND LACTONES THE CHANCELLORS, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD (GB) 2007-03-01 WO disclosed
US-20060165636-A1 Hair treatment composition and hair cosmetic for damaged hair MEIJI SEIKA KAISHA, LTD. (JP) 2006-07-27 US disclosed
US-20060018867-A1 Cosmetic composition and production thereof ICHIMARU PHARCOS CO., LTD 2006-01-26 US disclosed
EP-1604647-A1 Cosmetic composition containing polyorganosiloxane-containing epsilon-polylysine polymer, and polyhydric alcohol, and production thereof Ichimaru Pharcos Co., Ltd. (JP) 2005-12-14 EP disclosed
EP-1602354-A1 HAIR TREATMENT COMPOSITION AND HAIR COSMETIC FOR DAMAGED HAIR Meiji Seika Kaisha, Ltd. (JP) 2005-12-07 EP disclosed
US-6562514-B1 Stabilized vanadium electrolyte solutions for all-vanadium redox cells and batteries PINNACLE VRB LIMITED (AU) 2003-05-13 US disclosed
US-6468688-B2 CHARGING, DISCHARGING EFFICIENCY; VANADIUM ELECTROLYTE PINNACLE VRB LIMITED (AU) 2002-10-22 US disclosed
US-20010028977-A1 Charging, discharging efficiency; vanadium electrolyte JD HOLDING INC. (KY) 2001-10-11 US disclosed
CN-1289778-A Synthesis of ketonic acid lactone amino carbomate antibiotics PFIZER PROD INC (US) 2001-04-04 CN disclosed
US-6143443-A ALL-VANADIUM REDOX BATTERY, COMPRISING THE STABILIZED ELECTROLYTE PINNACLE ARB LIMITED (AU) 2000-11-07 US disclosed
EP-0682038-A1 5-O-DESOSAMINYLERYTHRONOLIDE DERIVATIVE TAISHO PHARMACEUTICAL CO. LTD (JP) 1995-11-15 EP disclosed