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The substrate phosphinothricin is used as a nonselective herbicide and is a potent inhibitor of EC 6.3.1.2, glutamate-ammonia ligase, a key enzyme of nitrogen metabolism in plants. Group: Enzymes. Synonyms: PAT; PPT acetyltransferase; Pt-N-acetyltransferase; ac-Pt. Enzyme Commission Number: EC 2.3.1.183. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2125; phosphinothricin acetyltransferase; EC 2.3.1.183; PAT; PPT acetyltransferase; Pt-N-acetyltransferase; ac-Pt. Cat No: EXWM-2125.
DL-Phosphinothricin
25g Pack Size. Group: Analytical Reagents, Biochemicals, Diagnostic Raw Materials. Formula: C5H15N2O4P. CAS No. 77182-82-2. Prepack ID 39868568-25g. Molecular Weight 198.16. See USA prepack pricing.
DL-Phosphinothricin ammonium salt
Used as a herbicide. Group: Biochemicals. Alternative Names: 2-Amino-4- (hydroxy methyl phosphinyl) butanoic Acid Ammonium Salt; Ammonium Glufosinate; Basta 150SL; Basta Fl; Basta LS; Buster; Dash; Finale; Glufosinate Monoammonium Salt; Glufosinate Ammonium; HOE 00661; HOE 39866; Ignite; Liberty. Grades: Highly Purified. CAS No. 77182-82-2. Pack Sizes: 50g, 100g, 250g, 500g. Molecular Formula: C?H??N?O?P, Molecular Weight: 198.16. US Biological Life Sciences.
Worldwide
2-hydroxyethylphosphonate dioxygenase
Requires non-heme-Fe(II). Isolated from some bacteria including Streptomyces hygroscopicus and Streptomyces viridochromogenes. The pro-R hydrogen at C-2 of the ethyl group is retained by the formate ion. Any stereochemistry at C-1 of the ethyl group is lost. One atom from dioxygen is present in each product. Involved in phosphinothricin biosynthesis. Group: Enzymes. Synonyms: HEPD; phpD (gene name); 2-hydroxyethylphosphonate:O2 1,2-oxidoreductase (hydroxymethylphosphonate forming). Enzyme Commission Number: EC 1.13.11.72. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0592; 2-hydroxyethylphosphonate dioxygenase; EC 1.13.11.72; HEPD; phpD (gene name); 2-hydroxyethylphosphonate:O2 1,2-oxidoreductase (hydroxymethylphosphonate forming). Cat No: EXWM-0592.
Desamino Glufosinate-d3
Phosphinothricin metabolite. Group: Biochemicals. Alternative Names: 4- (Hydroxy methyl phosphinyl) -butanoic Acid-d3. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Glufosinate ammonium
Glufosinate ammonium, a phosphinic acid analogue of glutamic acid, is an herbicide which is converted by plant cells into PT (L-phosphinothricin). Glufosinate ammonium exerts neurotoxic activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 77182-82-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W019870.
Glufosinate-d3 Hydrochloride
Labeled Glufosinate. Used as a herbicide. Group: Biochemicals. Alternative Names: 2-Amino-4- (hydroxy methyl phosphinyl) butanoic Acid Hydrochloride; DL-Phosphinothricin Hydrochloride. Grades: Highly Purified. CAS No. 59542-49-3. Pack Sizes: 1mg. Molecular Formula: C?H??D?ClNO?P, Molecular Weight: 220.61. US Biological Life Sciences.
Worldwide
L-Glufosinate
L-Glufosinate is a glutamine synthetase inhibitor and is used as a herbicide (usually as the corresponding ammonium or sodium salt, known as glufosinate-P-ammonium and glufosinate-P-sodium, respectively) to control annual weeds and grasses. Synonyms: Butanoic acid, 2-amino-4-(hydroxymethylphosphinyl)-, (2S)-; Glufosinate-P; (S)-Phosphinothricin; L-Phosphinothricin; (S)-Glufosinate; (+)-glufosinate; L-homoalanin-4-yl(methyl)phosphinic acid; 4-[hydroxy(methyl)phosphinoyl]-L-homoalanine; L-2-Amino-4-(hydroxymethylphosphinyl)butanoate-; (S)-2-Amino-4-(hydroxymethylphosphinyl)butyric acid. Grades: ≥95%. CAS No. 35597-44-5. Molecular formula: C5H12NO4P. Mole weight: 181.13.
phosphinomethylmalate isomerase
The enzyme, characterized from the bacterium Streptomyces viridochromogenes, is involved in bialaphos biosynthesis. The enzyme from the bacterium Kitasatospora phosalacinea participates in the biosynthesis of the related compound phosalacine. Both compounds contain the nonproteinogenic amino acid L-phosphinothricin that acts as a potent inhibitor of EC 6.3.1.2, glutamine synthetase. The similar enzyme EC 4.2.1.3, aconitate hydratase, cannot catalyse this reaction. Group: Enzymes. Synonyms: pmi (gene name). Enzyme Commission Number: EC 4.2.1.166. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5007; phosphinomethylmalate isomerase; EC 4.2.1.166; pmi (gene name). Cat No: EXWM-5007.
phosphonoacetaldehyde reductase (NADH)
The enzyme from Streptomyces viridochromogenes catalyses a step in the biosynthesis of phosphinothricin tripeptide, the reduction of phosphonoacetaldehyde to 2-hydroxyethylphosphonate. The preferred cofactor is NADH, lower activity with NADPH. Group: Enzymes. Synonyms: PhpC. Enzyme Commission Number: EC 1.1.1.309. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0220; phosphonoacetaldehyde reductase (NADH); EC 1.1.1.309; PhpC. Cat No: EXWM-0220.
phosphonoformate cytidylyltransferase
The enzyme, characterized from the bacterium Streptomyces viridochromogenes, participates in the biosynthesis of the herbicide antibiotic bialaphos. The enzyme from the bacterium Kitasatospora phosalacinea participates in the biosynthesis of the related compound phosalacine. Both compounds contain the nonproteinogenic amino acid L-phosphinothricin that acts as a potent inhibitor of EC 6.3.1.2, glutamine synthetase. Group: Enzymes. Synonyms: phpF (gene name). Enzyme Commission Number: EC 2.7.7.93. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3307; phosphonoformate cytidylyltransferase; EC 2.7.7.93; phpF (gene name). Cat No: EXWM-3307.
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