- DL-PROPARGYLGLYCINE
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- $10.00
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2019-07-06
- CAS:64165-64-6
- Min. Order: 10KG
- Purity: 99%
- Supply Ability: 100kg
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| | DL-Propargylglycine Basic information |
| Product Name: | DL-Propargylglycine | | Synonyms: | H-PROPARGYL-DL-GLYCINE;H-PROPARGYL-DL-GLY-OH;H-DL-PRA-OH;H-DL-GLY(PROPARGYL)-OH;DL-PROPARGYL-GLY-OH;2-AMINO-4-PENTYNOIC ACID;NSC21940;DL-Propargylglycine hydrochloride | | CAS: | 64165-64-6 | | MF: | C5H7NO2 | | MW: | 113.11 | | EINECS: | | | Product Categories: | Amino Acids | | Mol File: | 64165-64-6.mol |  |
| | DL-Propargylglycine Chemical Properties |
| storage temp. | -20°C | | solubility | Soluble in DMSO (up to 10 mg/ml) or in Water (up tp 10 mg/ml). | | form | Crystalline Powder | | color | White to off-white | | Stability: | Stable for 2 years from date of purchase as supplied. Solutions in DMSO or distilled water may be stored at -20° for up to 3 months. | | Major Application | cell analysis | | InChI | InChI=1S/C5H7NO2/c1-2-3-4(6)5(7)8/h1,4H,3,6H2,(H,7,8) | | InChIKey | DGYHPLMPMRKMPD-UHFFFAOYSA-N | | SMILES | C(N)(C(=O)O)CC#C |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | DL-Propargylglycine Usage And Synthesis |
| Description | Propargylglycine (64165-64-6) is an irreversible inhibitor of the hydrogen sulfide biosynthesis enzyme, cystathione-γ-lyase. It inhibits H2S production in rat liver preparations (IC50=55 μM) and inhibits the rise in plasma H2S in rats with hemorrhagic shock2. Propargylglycine reduces inflammation in a rodent carrageenan-induced hindpaw edema model3 and ameliorates gentamycin-induced nephrotoxicity1. | | Chemical Properties | White to off-white powder | | Uses | Dl-propargylglycine is an inhibitor of hydrogen sulfide (H2S) production. | | Synthesis Reference(s) | Journal of the American Chemical Society, 76, p. 3484, 1954 DOI: 10.1021/ja01642a036
Tetrahedron Letters, 22, p. 1787, 1981 DOI: 10.1016/S0040-4039(01)90439-3 | | Biochem/physiol Actions | DL-Propargylglycine (PAG) is an irreversible inhibitor of the enzyme cystathionine γ-lyase (GCL), a key enzyme involved in glutathione synthesis and the metabolic transsulfuration pathway which regulates homocysteine concentration and mediates cysteine synthesis. Treatment of animal disease models with PAG was shown to alleviate symptoms of diseases that impair the formation or action of hydrogen sulfide (H2S). | | References | [1] VAN P. DAM . Inhibition of cystathionine gamma-lyase and the biosynthesis of endogenous hydrogen sulphide ameliorates gentamicin-induced nephrotoxicity[J]. European journal of pharmacology, 2012, 685 1: Pages 165-173. DOI:10.1016/j.ejphar.2012.04.030
[2] YING-YUAN PAMELA MOK. Role of hydrogen sulphide in haemorrhagic shock in the rat: protective effect of inhibitors of hydrogen sulphide biosynthesis[J]. British Journal of Pharmacology, 2009, 143 7: 881-889. DOI:10.1038/sj.bjp.0706014
[3] MADHAV BHATIA. Hydrogen sulphide is a mediator of carrageenan-induced hindpaw oedema in the rat[J]. British Journal of Pharmacology, 2009, 145 2: 141-144. DOI:10.1038/sj.bjp.0706186 |
| | DL-Propargylglycine Preparation Products And Raw materials |
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