SCHEMBL2132802

SCHEMBL2132802

C=C[PH](=O)OCC

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
SCHEMBL27744493 0.79
SCHEMBL15144227 0.74
Butadiene SCHEMBL11349916 0.72
Propene SCHEMBL27744499 0.72
SCHEMBL28985834 0.72 LPAR3 (0.41)
SCHEMBL9152914 0.72
Ethyl Hydrogen Phosphonate SCHEMBL28723084 0.71
Ethyl Hydrogen Phosphonate SCHEMBL5934786 0.70 LMNA (0.46)
SCHEMBL17369252 0.70
SCHEMBL779859 0.70

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2010135141-A1 RECOVERY OF PHOSPHORUS VALUES AND SALT IMPURITIES FROM AQUEOUS WASTE STREAMS MONSANTO TECHNOLOGY LLC (US) 2010-11-25 WO claimed
US-10428092-B2 Process of producing phosphinothricin employing nitrilases STRATEGIC ENZYME APPLICATIONS, INC. (US) 2019-10-01 US disclosed
US-20170247399-A1 PROCESS OF PRODUCING PHOSPHINOTHRICIN EMPLOYING NITRILASES STRATEGIC ENZYME APPLICATIONS, INC. (US) 2017-08-31 US disclosed
US-9683001-B2 Process of producing phosphinothricin employing nitrilases Stragegic Enzyme Applications, Inc. (US) 2017-06-20 US disclosed
US-9394173-B2 Recovery of phosphorus values and salt impurities from aqueous waste streams MONSANTO TECHNOLOGY LLC (US) 2016-07-19 US disclosed
US-9227187-B2 Method for preparing proton-conducting inorganic particles COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES (FR) 2016-01-05 US disclosed
US-20150239917-A1 Process of Producing Phosphinothricin Employing Nitrilases STRATEGIC ENZYME APPLICATIONS, INC. (US) 2015-08-27 US disclosed
US-8981142-B2 Process of producing phosphinothricin employing nitrilases STRATEGIC ENZYME APPLICATIONS, INC. (US) 2015-03-17 US disclosed
US-20140234196-A1 RECOVERY OF PHOSPHORUS VALUES AND SALT IMPURITIES FROM AQUEOUS WASTE STREAMS MONSANTO TECHNOLOGY LLC (US) 2014-08-21 US disclosed
US-20140113982-A1 METHOD FOR PREPARING PROTON-CONDUCTING INORGANIC PARTICLES Commissariat à l'énergie atomique et aux énergies alternatives (FR) 2014-04-24 US disclosed
US-20120100051-A1 RECOVERY OF PHOSPHORUS VALUES AND SALT IMPURITIES FROM AQUEOUS WASTE STREAMS MONSANTO TECHNOLOGY LLC (US) 2012-04-26 US disclosed
WO-2011129820-A1 PROCESS FOR PRODUCING PHOSPHINOTHRICIN EMPLOYING NITRILASES STRATEGIC ENZYME APPLICATIONS, INC. (US) 2011-10-20 WO disclosed
WO-2010135141-A1 RECOVERY OF PHOSPHORUS VALUES AND SALT IMPURITIES FROM AQUEOUS WASTE STREAMS MONSANTO TECHNOLOGY LLC (US) 2010-11-25 WO disclosed
US-6506738-B1 Treatment of viral infections. More particularly, the invention provides benzimidazolone derivatives for the treatment of respiratory syncytial virus infection. BRISTOL-MYERS SQUIBB COMPANY 2003-01-14 US disclosed
WO-2002026228-A1 BENZIMIDAZOLONE ANTIVIRAL AGENTS BRISTOL-MYERS SQUIBB COMPANY (US) 2002-04-04 WO disclosed
EP-0907666-A1 PARTICLES COMPRISING AMPHIPHILIC COPOLYMERS, HAVING A CROSS-LINKED SHELL DOMAIN AND AN INTERIOR CORE DOMAIN, USEFUL FOR PHARMACEUTICAL AND OTHER APPLICATIONS G.D. Searle & Co. (US) 1999-04-14 EP disclosed
WO-1997049736-A2 PARTICLES COMPRISING AMPHIPHILIC COPOLYMERS, HAVING A CROSS-LINKED SHELL DOMAIN AND AN INTERIOR CORE DOMAIN, USEFUL FOR PHARMACEUTICAL AND OTHER APPLICATIONS G.D. SEARLE AND CO. (US) 1997-12-31 WO disclosed
EP-0127429-B1 PROCESS FOR PREPARING OPTICALLY ACTIVE ((3-AMINO-3-CARBOXY)PROPYL-1) PHOSPHINIC ACID DERIVATIVES MEIJI SEIKA KAISHA LTD. (JP) 1989-04-19 EP disclosed
US-4499027-A REACTING A SHIFF'S BASE AND AN ALKYL VINYL PHOSPHINATE USING A BASIC CATALYST; HYDROLYSIS; STEREOSPECIFIC MEIJI SEIKA KAISHA, LTD. (JP) 1985-02-12 US disclosed
EP-0127429-A2 Process for preparing optically active ((3-amino-3-carboxy)propyl-1) phosphinic acid derivatives MEIJI SEIKA KAISHA LTD. (JP) 1984-12-05 EP disclosed