860794
Z-L-苯丙氨酸氯甲酮
98%
别名:
N-苄氧羰基-L-苯丙氨酰甲基氯酮, ZPCK
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关于此项目
线性分子式:
C6H5CH2CH(NHCO2CH2C6H5)COCH2Cl
化学文摘社编号:
分子量:
331.79
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
247-432-8
MDL number:
InChI key
OYHLRJGDELITAF-INIZCTEOSA-N
InChI
1S/C18H18ClNO3/c19-12-17(21)16(11-14-7-3-1-4-8-14)20-18(22)23-13-15-9-5-2-6-10-15/h1-10,16H,11-13H2,(H,20,22)/t16-/m0/s1
SMILES string
ClCC(=O)[C@H](Cc1ccccc1)NC(=O)OCc2ccccc2
assay
98%
form
powder
optical activity
[α]23/D +30°, c = 1 in chloroform
reaction suitability
reaction type: solution phase peptide synthesis
mp
107-108 °C (lit.)
application(s)
peptide synthesis
storage temp.
−20°C
Quality Level
Application
酶抑制剂。
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Inhibition of carboxypeptidase Y by chloromethyl ketone derivatives of benzyloxycarbonyl-L-phenylalanine.
R Hayashi et al.
Journal of biochemistry, 76(6), 1355-1357 (1974-12-01)
L A Johnson et al.
Biochimica et biophysica acta, 953(3), 269-279 (1988-04-14)
The reaction of chymase, a chymotryptic proteinase from human skin, and bovine pancreatic chymotrypsin with a number of time-dependent inhibitors has been studied. An integrated equation, relating product formation with time, has been derived for the reaction of enzymes with
G Jung et al.
Protein science : a publication of the Protein Society, 4(11), 2433-2435 (1995-11-01)
The essential histidine residue of carboxypeptidase Y (CPY) was modified by a site-specific reagent, a chloromethylketone derivative of benzyloxycarbonyl-L-phenylalanine. The single modified histidine residue was converted to N tau-carboxy-methyl histidine (cmHis) upon performic acid oxidation. A peptide containing cmHis was
Biogenesis of vaccina: interrelationship between post-translational cleavage, virus assembly, and maturation.
M Silver et al.
Virology, 117(2), 341-356 (1982-03-01)
J Brtko et al.
Endocrine regulations, 26(3), 127-131 (1992-09-01)
The effect of protease inhibitors N-tosyl-L-phenylalanine chloromethyl ketone (TPCK) and N-carbobenzoxy-L-phenylalanine chloromethyl ketone (ZPCK) at concentrations ranging from 1.5 x 10(-6) mol/l to 1.5 x 10(-4) mol/l on the specific binding of 3,5,3'-triiodothyronine (T3) to rat liver nuclear receptors was
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