135093-66-2 Usage
Description
N-acetyldemethylphosphinothricin, also known as NADP, is a synthetic organic compound that functions as a potent herbicide. It is derived from phosphinothricin, the active ingredient in the herbicide glufosinate. NADP effectively inhibits the enzyme glutamine synthetase, which is crucial for the synthesis of the amino acid glutamine in plants. By preventing the production of glutamine, NADP ensures that plants cannot survive, making it a fast-acting and efficient herbicide. It is characterized by its broad-spectrum activity and rapid onset, and it is considered to have low toxicity to humans and animals, making it suitable for various herbicide formulations in crop protection.
Uses
Used in Agricultural Applications:
N-acetyldemethylphosphinothricin is used as a herbicide for [application reason] controlling a wide range of weeds in agricultural settings. Its broad-spectrum activity and rapid onset of action make it an effective tool for crop protection, ensuring healthy crop growth by eliminating unwanted plant competition.
Used in Herbicide Formulations:
N-acetyldemethylphosphinothricin is used as an active ingredient in various herbicide formulations for [application reason] providing farmers with a reliable means of controlling weeds and safeguarding their crops. Its low toxicity to humans and animals makes it a preferred choice for agricultural use, minimizing potential harm to non-target organisms while effectively managing weed populations.
Check Digit Verification of cas no
The CAS Registry Mumber 135093-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,9 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135093-66:
(8*1)+(7*3)+(6*5)+(5*0)+(4*9)+(3*3)+(2*6)+(1*6)=122
122 % 10 = 2
So 135093-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H10NO5P/c1-4(8)7-5(6(9)10)2-3-13(11)12/h5H,2-3H2,1H3,(H2-,7,8,9,10,11,12)/p+1/t5-/m0/s1
135093-66-2Relevant articles and documents
Spectroscopic characterization and mechanistic investigation of P-methyl transfer by a radical SAM enzyme from the marine bacterium Shewanella denitrificans OS217
Allen, Kylie D.,Wang, Susan C.
, p. 2135 - 2144 (2014)
Natural products containing carbon-phosphorus bonds elicit important bioactivity in many organisms. l-Phosphinothricin contains the only known naturally-occurring carbon-phosphorus-carbon bond linkage. In actinomycetes, the cobalamin-dependent radical S-adenosyl-l-methionine (SAM) methyltransferase PhpK catalyzes the formation of the second C-P bond to generate the complete C-P-C linkage in phosphinothricin. Here we use electron paramagnetic resonance and nuclear magnetic resonance spectroscopies to characterize and demonstrate the activity of a cobalamin-dependent radical SAM methyltransferase denoted SD-1168 from Shewanella denitrificans OS217, a marine bacterium that has not been reported to synthesize phosphinothricin. Recombinant, refolded, and reconstituted SD-1168 binds a four-iron, four-sulfur cluster that interacts with SAM and cobalamin. In the presence of SAM, a reductant, and methylcobalamin, SD-1168 surprisingly catalyzes the P-methylation of N-acetyl-demethylphosphinothricin and demethylphosphinothricin to produce N-acetyl-phosphinothricin and phosphinothricin, respectively. In addition, this enzyme is active in the absence of methylcobalamin if the strong reductant titanium (III) citrate and hydroxocobalamin are provided. When incubated with [methyl-13C] cobalamin and titanium citrate, both [methyl-13C] and unlabeled N-acetylphosphinothricin are produced. Our results suggest that SD-1168 catalyzes P-methylation using radical SAM-dependent chemistry with cobalamin as a coenzyme. In light of recent genomic information, the discovery of this P-methyltransferase suggests that S. denitrificans produces a phosphinate natural product.
