SCHEMBL4986090

SCHEMBL4986090

CCC(C=O)O[Si](C)(C)C(C)(C)C

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
SCHEMBL4570487 1.00
Toluene SCHEMBL5000851 0.84 LMNA (0.32)
SCHEMBL2174728 0.80
SCHEMBL2174724 0.80
SCHEMBL7595079 0.80 CA2 (0.36)
SCHEMBL15490985 0.79
SCHEMBL16796788 0.79
SCHEMBL16796789 0.79
SCHEMBL4936168 0.78 ADH1B (0.36)
SCHEMBL1521495 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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250027123-A1 Compositions, Systems, and Methods for Performing a Mannich Cyclization Reaction THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2025-01-23 US disclosed
US-9809566-B2 Organocatalytic process for asymmetric synthesis of decanolides COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2017-11-07 US disclosed
US-9765048-B2 Organocatalytic process for asymmetric synthesis of decanolides COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2017-09-19 US disclosed
US-20160272608-A1 ORGANOCATALYTIC PROCESS FOR ASYMMETRIC SYNTHESIS OF DECANOLIDES COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2016-09-22 US disclosed
US-20160272609-A1 ORGANOCATALYTIC PROCESS FOR ASYMMETRIC SYNTHESIS OF DECANOLIDES COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2016-09-22 US disclosed
US-20150175530-A1 ANTIBACTERIAL AGENTS ACHAOGEN, INC. 2015-06-25 US disclosed
US-20110245528-A1 THERAPEUTIC COMPOUNDS SCHWARTZ C ERIC 2011-10-06 US disclosed
US-20080207936-A1 Chemical intermediate for drugs; reduction of the corresponding 3-hydroxybutyrate ; then oxidation using nitroxyl compound and co-oxidizer KANEKA CORPORATION (JP) 2008-08-28 US disclosed
EP-1862465-A1 METHOD OF PRODUCING 3-HYDROXYBUTYRALDEHYDE DERIVATIVE Kaneka Corporation (JP) 2007-12-05 EP disclosed
US-5336771-A Certain 3,4-dihydro-2H-pyrano[2,3-b]pyridines PFIZER INC. (US) 1994-08-09 US disclosed