Details
Stereochemistry | ACHIRAL |
Molecular Formula | C2H8NO3P |
Molecular Weight | 125.0636 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NCCP(O)(O)=O
InChI
InChIKey=QQVDJLLNRSOCEL-UHFFFAOYSA-N
InChI=1S/C2H8NO3P/c3-1-2-7(4,5)6/h1-3H2,(H2,4,5,6)
Molecular Formula | C2H8NO3P |
Molecular Weight | 125.0636 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Rapid automatic NCS identification using heavy-atom substructures. | 2002 Dec |
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Binding of phosphorothioate oligonucleotides to zwitterionic liposomes. | 2002 Jun 13 |
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High performance carbon-supported catalysts for fuel cells via phosphonation. | 2003 Apr 7 |
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A role for carbon catabolite repression in the metabolism of phosphonoacetate by Agromyces fucosus Vs2. | 2006 Aug |
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Diversification of function in the haloacid dehalogenase enzyme superfamily: The role of the cap domain in hydrolytic phosphoruscarbon bond cleavage. | 2006 Dec |
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GABA-mediated effects of some taurine derivatives injected i.c.v. on rabbit rectal temperature and gross motor behavior. | 2006 May |
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Structures of an alanine racemase from Bacillus anthracis (BA0252) in the presence and absence of (R)-1-aminoethylphosphonic acid (L-Ala-P). | 2008 May 1 |
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Hydroperoxylation by hydroxyethylphosphonate dioxygenase. | 2009 Nov 11 |
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Structural analysis of O-glycans of mucin from jellyfish (Aurelia aurita) containing 2-aminoethylphosphonate. | 2009 Nov 2 |
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The ethanolamine branch of the Kennedy pathway is essential in the bloodstream form of Trypanosoma brucei. | 2009 Sep |
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Seasonal Expression of the Picocyanobacterial Phosphonate Transporter Gene phnD in the Sargasso Sea. | 2010 |
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Comparative study on the rumen microbial populations, hydrolytic enzyme activities and dry matter degradability between different species of ruminant. | 2010 Dec |
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A new amido phosphonate derivative of carboxymethylcellulose with an osteogenic activity and which is capable of interacting with any Ti surface. | 2010 Oct |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:12:24 GMT 2023
by
admin
on
Fri Dec 15 19:12:24 GMT 2023
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Record UNII |
AH00YJQ334
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Record Status |
Validated (UNII)
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Record Version |
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218-043-0
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DTXSID10174362
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AH00YJQ334
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admin on Fri Dec 15 19:12:24 GMT 2023 , Edited by admin on Fri Dec 15 19:12:24 GMT 2023
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