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About This Item
经验公式（希尔记法）:
C5H7NO2
CAS号:
分子量:
113.11
Beilstein:
2347861
MDL號碼:
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
NACRES:
NA.26
推荐产品
product name
L-C-炔丙基甘氨酸, ≥99.0% (TLC)
化驗
≥99.0% (TLC)
形狀
powder
顏色
white
mp
235-239 °C
應用
peptide synthesis
儲存溫度
2-8°C
SMILES 字串
N[C@@H](CC#C)C(O)=O
InChI
1S/C5H7NO2/c1-2-3-4(6)5(7)8/h1,4H,3,6H2,(H,7,8)/t4-/m0/s1
InChI 密鑰
DGYHPLMPMRKMPD-BYPYZUCNSA-N
應用
用于 γ-胱硫醚酶不可逆失活的试剂；γ-胱硫醚酶和其他酶的亲和标记试剂；含有该氨基酸的肽可以被氚化至高比放射性
生化／生理作用
L-炔丙基甘氨酸（PAG）是胱硫醚 γ-裂解酶（CSE）的抑制剂，可用于研究硫化氢的合成和生物活性。
L-炔丙基甘酸是一种特异性的 H（2）S 合酶胱硫醚-γ-裂解酶（CSE）的抑制剂，可用于研究 H2S 在生物学过程调节中的作用。
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
Bridget Fox et al.
Journal of cellular and molecular medicine, 16(4), 896-910 (2011-06-18)
Hydrogen sulfide (H(2)S) has recently been proposed as an endogenous mediator of inflammation and is present in human synovial fluid. This study determined whether primary human articular chondrocytes (HACs) and mesenchymal progenitor cells (MPCs) could synthesize H(2)S in response to
A.N. Eberle et al.
Helvetica Chimica Acta, 68, 1880-1880 (1985)
Metabolic consequences of affinity labeling of cystathionase and alanine aminotransferase by L-propargylglycine in vivo.
S Shinozuka et al.
European journal of biochemistry, 124(2), 377-382 (1982-05-17)
Mechanism of inactivation of gamma-cystathionase by the acetylenic substrate analogue propargylglycine.
W Washtien et al.
Biochemistry, 16(11), 2485-2491 (1977-05-31)
Shiau Wei Lee et al.
Glia, 54(2), 116-124 (2006-05-24)
Hydrogen sulphide (H2S), which is produced endogenously from L-cysteine in mammalian tissues, has been suggested to function as a neuromodulator in the brain. However, the role of H2S in microglial cells is unclear. In this study, the effect of exogenous
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