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Merck
CN

SML2027

Sigma-Aldrich

L-2-oxothiazolidine-4-carboxylic acid propargyl amide

≥98% (HPLC)

别名:

(R)-2-Oxo-N-2-propyn-1-yl-4-thiazolidinecarboxamide, OTC propargyl amide, OTC-PA

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About This Item

经验公式(希尔记法):
C7H8N2O2S
分子量:
184.22
MDL编号:
UNSPSC代码:
12352106
NACRES:
NA.77

方案

≥98% (HPLC)

表单

powder

颜色

white to beige

溶解性

H2O: 2 mg/mL, clear

储存温度

2-8°C

SMILES字符串

C#CCNC([C@@H]1CSC(N1)=O)=O

InChI

1S/C7H8N2O2S/c1-2-3-8-6(10)5-4-12-7(11)9-5/h1,5H,3-4H2,(H,8,10)(H,9,11)/t5-/m0/s1

InChI key

MWEQVHWJNCRXGP-YFKPBYRVSA-N

生化/生理作用

L-2-oxothiazolidine-4-carboxylic acid propargyl amide is a cell penetrant, potent and selective competitive inhibitor of cystathionine-γ-lyase that completely abrogated L-cysteine-induced vasorelaxation in tissue.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Angela Corvino et al.
Scientific reports, 6, 34398-34398 (2016-10-07)
Hydrogen sulfide is an essential catabolite that intervenes in the pathophysiology of several diseases from hypertension to stroke, diabetes and pancreatitis. It is endogenously synthesized mainly by two pyridoxal-5'-phosphate-dependent enzymes involved in L-cysteine metabolism: cystathionine-ß-synthase (CBS) and cystathionine-γ-lyase (CSE). Research

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