推薦產品
product name
N-乙酰基-L-脯氨酸,
化驗
≥98% (TLC)
品質等級
形狀
powder
技術
ligand binding assay: suitable
顏色
white
儲存溫度
2-8°C
SMILES 字串
CC(=O)N1CCC[C@H]1C(O)=O
InChI
1S/C7H11NO3/c1-5(9)8-4-2-3-6(8)7(10)11/h6H,2-4H2,1H3,(H,10,11)/t6-/m0/s1
InChI 密鑰
GNMSLDIYJOSUSW-LURJTMIESA-N
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相關類別
生化/生理作用
N-乙酰基-L-脯氨酸是血管紧张素转化酶(ACE)优选底物的一种COOH-末端二肽部分类似物。它可用于研究底物和抑制剂通过ACE的结合,并区分出各种氨基酰基酶的特异性。
N-乙酰基-L-脯氨酸,一种血管紧张素转化酶优选底物COOH-末端二肽部分的类似物,可用于探测血管紧张素转化酶的活性位点。N-乙酰基-L-脯氨酸可用于鉴定、区分和表征N-酰基-氨基酸酰胺水解酶/氨基酰化酶。N-乙酰基-L-脯氨酸可用于研究脯氨酸的理化参数。
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)
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
The journal of physical chemistry. B, 111(50), 14034-14042 (2007-11-22)
The results of the ring conformational analysis of L-proline, N-acetyl-L-proline, and trans-4-hydroxy-L-proline by NMR combined with calculations using density functional theory (DFT) and molecular dynamics (MD) are reported. Accurate values of 1H-1H J-couplings in water and other solvents have been
Journal of medicinal chemistry, 31(6), 1148-1160 (1988-06-01)
Analogues of captopril, enalaprilat, and the phosphinic acid [hydroxy(4-phenylbutyl)phosphinyl]acetyl]-L-proline incorporating 4-substituted proline derivatives have been synthesized and evaluated as inhibitors of angiotensin-converting enzyme (ACE) in vitro and in vivo. The 4-substituted prolines, incorporating alkyl, aryl, alkoxy, aryloxy, alkylthio, and arylthio
Bioscience, biotechnology, and biochemistry, 69(10), 1914-1922 (2005-10-26)
A novel aminoacylase was purified to homogeneity from culture broth of Streptomyces mobaraensis, as evidenced by SDS-polyacrylamide gel electrophoresis (PAGE). The enzyme was a monomer with an approximate molecular mass of 100 kDa. The purified enzyme was inhibited by the
The journal of physical chemistry. B, 112(11), 3441-3450 (2008-02-26)
The structure and properties of (s)-N-acetylproline amide (NAP) in aqueous solution are studied by exploiting a continuum solvation model. The conformational preference of NAP as a function of the environment is discussed as well as data for a number of
International journal of pharmaceutics, 192(2), 147-158 (1999-11-24)
A series of N-acetylproline esters (alkyl side chain length, 5-18) were synthesized and tested for potential skin penetration enhancement activity using modified Franz diffusion cells and hairless mouse skin as the penetration barrier. Benazepril and hydrocortisone were used as model
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