S8511
N-琥珀酰-丙酰氨-丙酰氨-脯酰氨-亮氨酸对硝基酰苯胺
protease substrate, solid
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关于此项目
经验公式（希尔记法）:
C27H38N6O9
化学文摘社编号:
分子量:
590.63
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.32
MDL number:
产品名称
N-琥珀酰-丙酰氨-丙酰氨-脯酰氨-亮氨酸对硝基酰苯胺, protease substrate
SMILES string
CC(C)CC(NC(=O)C1CCCN1C(=O)C(C)NC(=O)C(C)NC(=O)CCC(O)=O)C(=O)Nc2ccc(cc2)N(=O)=O
InChI
1S/C27H38N6O9/c1-15(2)14-20(25(38)30-18-7-9-19(10-8-18)33(41)42)31-26(39)21-6-5-13-32(21)27(40)17(4)29-24(37)16(3)28-22(34)11-12-23(35)36/h7-10,15-17,20-21H,5-6,11-14H2,1-4H3,(H,28,34)(H,29,37)(H,30,38)(H,31,39)(H,35,36)
InChI key
PTHRPHGMGFMCSS-UHFFFAOYSA-N
form
solid
storage temp.
−20°C
Quality Level
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General description
弹性蛋白酶底物
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
常规特殊物品
此项目有
E G Del Mar et al.
Biochemistry, 19(3), 468-472 (1980-02-05)
The substrate specificity of human pancreatic elastase 2 was investigated by using a series of peptide p-nitroanilides. The kinetic constants, kcat and Km, for the hydrolysis of these peptides revealed that this serine protease preferentially hydrolyzes peptides containing P1 amino
Heba M Abdelgaffar et al.
Pesticide biochemistry and physiology, 153, 1-8 (2019-02-13)
The Cry1Ac protein is the most active insecticidal toxin from the bacterium Bacillus thuringiensis (Bt) to members of the heliothinae subfamily in Lepidoptera, which includes some of the most devastating pests of corn and cotton worldwide. However, there are wide
Qi-Juan Gu et al.
Journal of insect physiology, 116, 41-48 (2019-04-27)
To establish successful infections, endoparasitoid wasps must develop strategies to evade immune responses of the host. Here, we identified and characterized a teratocytes-expressed gene encoding a trypsin inhibitor-like protein containing a cysteine-rich domain from Cotesia vestalis, CvT-TIL. CvT-TIL had a
Fatemehsadat Esteghamat et al.
Nature genetics, 51(8), 1233-1243 (2019-07-31)
Factors that underlie the clustering of metabolic syndrome traits are not fully known. We performed whole-exome sequence analysis in kindreds with extreme phenotypes of early-onset atherosclerosis and metabolic syndrome, and identified novel loss-of-function mutations in the gene encoding the pancreatic
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