ChemicalBook--->CAS DataBase List--->16900-57-5

16900-57-5

16900-57-5 Structure

16900-57-5 Structure
IdentificationBack Directory
[Name]

DL-Propargylglycine
[CAS]

16900-57-5
[Synonyms]

DL-Propargylglycine HCl
DL-2-Propynylglycine hydrochloride
2-Amino-4-pentynoic acid hydrochloride
2-Aminopent-4-ynoic acid hydrochloride
2-amino-4-pentynoic Acid Hydrochloride (1:1)
[Molecular Formula]

C5H7NO2
[MOL File]

16900-57-5.mol
[Molecular Weight]

113.115
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

DMF: 20 mg/ml; DMSO: 20 mg/ml; Ethanol: 20 mg/ml; PBS (pH 7.2): 10 mg/ml
[form ]

A crystalline solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Description]

Hydrogen sulphide (H2S), a naturally occurring gasotransmitter, is a potent vasodilator and pro-inflammatory mediator. DL-Propargyl glycine (PAG) is an irreversible inhibitor of the H2S synthesizing enzyme cystathionine-γ-lyase (CSE). PAG blocks H2S synthesis activity in rat liver preparations with an IC50 value of 55 μM and abolishes the rise in plasma H2S in anaesthetized rats induced with hemorrhagic shock. At concentrations ranging from 25-100 mg/kg, PAG can reduce H2S-associated inflammation in rodent models of pancreatitis, oedema, and endotoxemia.
[Uses]

DL-Propargylglycine Hydrochloride is used in preparation of tert-Butoxycarbonyl Azide.
[storage]

Store at -20°C
[References]

[1] MADHAV BHATIA. Pro-inflammatory effects of hydrogen sulphide on substance P in caerulein-induced acute pancreatitis[J]. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2007, 12 2: 580-590. DOI: 10.1111/j.1582-4934.2007.00131.x
[2] 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
[3] MARIKA COLLIN. Inhibition of endogenous hydrogen sulfide formation reduces the organ injury caused by endotoxemia[J]. British Journal of Pharmacology, 2009, 146 4: 498-505. DOI: 10.1038/sj.bjp.0706367
Spectrum DetailBack Directory
[Spectrum Detail]

DL-Propargylglycine(16900-57-5)1HNMR
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