SCHEMBL2932270

SCHEMBL2932270

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

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
SCHEMBL55047 1.00
SCHEMBL791249 1.00
SCHEMBL1041254 1.00
SCHEMBL2107037 1.00
SCHEMBL55048 1.00
SCHEMBL5549445 1.00
SCHEMBL3518225 1.00
SCHEMBL2687210 1.00
Ammonia Solution, Strong SCHEMBL2340361 0.97
SCHEMBL28118146 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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240191265-A1 Beta-Lactone Production Through Bioconversion and Methods Related Thereto EXXONMOBIL TECHNOLOGY & ENGINEERING COMPANY (US) 2024-06-13 US claimed
WO-1991009959-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE 3-HYDROXY-2-METHYLBUTYRATES TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1991-07-11 WO claimed
US-20240191265-A1 Beta-Lactone Production Through Bioconversion and Methods Related Thereto EXXONMOBIL TECHNOLOGY & ENGINEERING COMPANY (US) 2024-06-13 US disclosed
US-20150051262-A1 NMDA RECEPTOR MODULATORS AND USES THEREOF NORTHWESTERN UNIVERSITY (US) 2015-02-19 US disclosed
EP-2230312-A1 Probe compound for detecting and isolating enzymes and means and methods using the same Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2010-09-22 EP disclosed
US-7432087-B2 Method for preparing (2S, 3R, 4S)-4-hydroxyisoleucine and analogues thereof CENTRE NATIONAL DE LA RECHERCHE SCIENTIFQUE (FR) 2008-10-07 US disclosed
EP-1268397-B1 METHOD FOR PREPARING (2S,3R,4S)-4-HYDROXYISOLEUCINE AND ANALOGUES THEREOF CENTRE NAT RECH SCIENT (FR) 2007-12-05 EP disclosed
US-20050079587-A1 Method for preparing (2S, 3R, 4S) -4-hydroxyisoleucine and analogues thereof CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE 2005-04-14 US disclosed
US-20030219880-A1 Method for preparing (2s,3r,4s)-4-hydroxyisoleucine and analogues thereof CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2003-11-27 US disclosed
EP-1268397-A2 METHOD FOR PREPARING (2S,3R,4S)-4-HYDROXYISOLEUCINE AND ANALOGUES THEREOF CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2003-01-02 EP disclosed
WO-2001072688-A2 METHOD FOR PREPARING (2S,3R,4S)-4-HYDROXYISOLEUCINE AND ANALOGUES THEREOF CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2001-10-04 WO disclosed
US-5328643-A Electrooptic display, switches, modulators; physical and chemical stability and spontaneous polarization TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1994-07-12 US disclosed
US-5232853-A METHOD FOR PRODUCING (2R,3S)-3-HYDROXY-2-METHYLBUTYRATE BY MICROBIAL REDUCTION TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1993-08-03 US disclosed
US-5232853-A METHOD FOR PRODUCING (2R,3S)-3-HYDROXY-2-METHYLBUTYRATE BY MICROBIAL REDUCTION TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1993-08-03 US disclosed
US-5167863-A Ferroelectricity; electrooptic switches HITACHI, LTD. (JP) 1992-12-01 US disclosed
WO-1991009959-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE 3-HYDROXY-2-METHYLBUTYRATES TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1991-07-11 WO disclosed
EP-0428392-A2 Optically active compounds having plural chiral centers and the production thereof Chisso Corporation (JP) 1991-05-22 EP disclosed
EP-0351782-A2 Optically active compounds liquid crystal composition containing said compound, and liquid crystal optical modulator using said composition HITACHI, LTD. (JP) 1990-01-24 EP disclosed
EP-0341713-A2 Optically active compounds, liquid crystal compositions comprising said compounds, and liquid crystal optical modulators using said compositions HITACHI, LTD. (JP) 1989-11-15 EP disclosed
EP-0322862-A2 Optically active compounds, their preparation and their use in liquid crystal compositions and liquid crystal optical modulators HITACHI, LTD. (JP) 1989-07-05 EP disclosed