Phosphinothricin
Phosphinothricin Basic information
- Product Name:
- Phosphinothricin
- Synonyms:
-
- 2-amino-4-(hydroxymethylphosphinyl)butyric acid
- Phosphinothricin
- Phosphinothricin ammonium salt
- 2-Amino-4-(methylhydroxyphosphinyl)butyric acid
- HOE-35956
- HOE-866
- C05042
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N
- CAS:
- 51276-47-2
- MF:
- C5H12NO4P
- MW:
- 181.13
- EINECS:
- 257-102-5
- Mol File:
- 51276-47-2.mol
Phosphinothricin Chemical Properties
- Melting point:
- 229-231° (dec)
- Boiling point:
- 519.1±45.0 °C(Predicted)
- Density
- 1.378±0.06 g/cm3(Predicted)
- solubility
- Aqueous Acid (Slightly), Methanol (Very Slightly, Sonicated), Water (Slightly)
- pka
- 2.22±0.10(Predicted)
- form
- Solid
- color
- White to Light Beige
- Stability:
- Hygroscopic
- LogP
- -0.750 (est)
- EPA Substance Registry System
- Butanoic acid, 2-amino-4-(hydroxymethylphosphinyl)- (51276-47-2)
Phosphinothricin Usage And Synthesis
Definition
ChEBI: 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid is a non-proteinogenic alpha-amino acid that is 2-aminobutanoic acid which is substituted at position 4 by a hydroxy(methyl)phosphoryl group. It is a member of phosphinic acids and a non-proteinogenic alpha-amino acid.
Enzyme inhibitor
This dephospho transition-state analogue (FW = 177.10 g/mol; CAS 51276- 47-2) is naturally occurring glutamate analogue, first isolated from Streptomyces viridochromogenes. Phosphonothricin is a slow, tight-binding inhibitor of glutamine synthetase that binds at the glutamate binding site and stabilizes the flap of a glutamyl residue in a position blocking glutamate entry into the active site, thereby trapping the inhibitor on the enzyme. Phosphinothricin undergoes an ATP-dependent phosphorylation. Note: Phosphinothricin is a component of the antibiotics bialaphos and phosalacine. The monoammonium salt of the racemic compound, also called glufosinate-ammonium, is a post-emergent herbicide.
Metabolic pathway
When 14C-phosphinothricin [homoalanin-4-yl- (methyl)phosphinic acid] is incubated in the cell suspension cultures of soybean, wheat, and maize, in maize cells which take up to 50% of the applied radioactivity, four different metabolites are detected which are identified as 4-methylphosphinico-2-oxo- butyric acid, 4-methylphosphinico-2-hydroxybutyric acid, 4-methylphosphinicobutyric acid, and 3- methylphosphinicopropionic acid. In soybean and wheat cultures, 10 and 6% of the applied radioactivity is taken up, respectively. In soybean, only one metabolite, 3-methylphosphinicopropionic acid, is detected, whereas in wheat, 4-methyl- phosphinicobutyric acid is additionally present.
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