SCHEMBL1964305

SCHEMBL1964305

COC(=O)C(C)(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
SCHEMBL2306970 0.81 HMGCR (0.32)
SCHEMBL3827004 0.79
SCHEMBL1063211 0.79
SCHEMBL27509282 0.79
SCHEMBL28869957 0.79
SCHEMBL769720 0.78 DGAT1 (0.44)
SCHEMBL14152581 0.77 DGAT1 (0.48)
SCHEMBL17801117 0.77 DGAT1 (0.44)
SCHEMBL3940490 0.77 DGAT1 (0.39)
SCHEMBL16057010 0.77 DGAT1 (0.39)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-100540476-C Method for recovering methacrylic acid from dilute aqueous methacrylic acid solution by reverse osmosis ARKEMA (FR) 2009-09-16 CN claimed
CN-1750996-A A process for the recovery of methacrylic acid from its aqueous diluted solutions by reverse osmosis ARKEMA (FR) 2006-03-22 CN claimed
US-9340493-B2 Hydroxamic acid derivatives useful as antibacterial agents PFIZER INC. (US) 2016-05-17 US disclosed
US-9340493-B2 Hydroxamic acid derivatives useful as antibacterial agents PFIZER INC. (US) 2016-05-17 US disclosed
US-9340493-B2 Hydroxamic acid derivatives useful as antibacterial agents PFIZER INC. (US) 2016-05-17 US disclosed
US-20150050227-A1 Compositions Having Perspiration Reduction Properties AMCOL INTERNATIONAL CORPORATION 2015-02-19 US disclosed
US-20140206651-A1 Hydroxamic Acid Derivatives Useful As Antibacterial Agents PFIZER INC. (US) 2014-07-24 US disclosed
US-20140206651-A1 Hydroxamic Acid Derivatives Useful As Antibacterial Agents PFIZER INC. (US) 2014-07-24 US disclosed
US-20140206651-A1 Hydroxamic Acid Derivatives Useful As Antibacterial Agents PFIZER INC. (US) 2014-07-24 US disclosed
US-8722686-B2 Hydroxamic acid derivatives useful as antibacterial agents PFIZER INC. (US) 2014-05-13 US disclosed
US-8722686-B2 Hydroxamic acid derivatives useful as antibacterial agents PFIZER INC. (US) 2014-05-13 US disclosed
WO-2010032147-A2 HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS PFIZER INC. (US) 2010-03-25 WO disclosed
US-7186854-B2 Process for making bicalutamide and intermediates thereof SYNTHON IP INC. (US) 2007-03-06 US disclosed
US-7186854-B2 Process for making bicalutamide and intermediates thereof SYNTHON IP INC. (US) 2007-03-06 US disclosed
US-7186854-B2 Process for making bicalutamide and intermediates thereof SYNTHON IP INC. (US) 2007-03-06 US disclosed
EP-1546093-A1 PROCESS FOR MAKING BICALUTAMIDE AND INTERMEDIATES THEREOF Synthon B.V. (NL) 2005-06-29 EP disclosed
US-6818766-B2 USING P-FLUOROBENZENESULFINIC ACID SYNTHON BV (NL) 2004-11-16 US disclosed
WO-2004031136-A1 PROCESS FOR MAKING BICALUTAMIDE AND INTERMEDIATES THEREOF SYNTHON B.V. (NL) 2004-04-15 WO disclosed
US-20040068135-A1 Process for making bicalutamide and intermediates thereof SYNTHON IP INC. 2004-04-08 US disclosed
US-20030073742-A1 Process for making bicalutamide and intermediates thereof SYNTHON B.V. (NL) 2003-04-17 US disclosed