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Merck
CN

46916

Sigma-Aldrich

芴甲氧羰酰胺

≥99.0% (HPLC)

别名:

Fmoc-酰胺

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About This Item

经验公式(希尔记法):
C15H13NO2
CAS号:
分子量:
239.27
Beilstein:
4188192
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22

方案

≥99.0% (HPLC)

表单

solid

mp

201-204 °C

溶解性

dioxane: 15 mg/mL, clear, colorless

应用

peptide synthesis

SMILES字符串

NC(=O)OCC1c2ccccc2-c3ccccc13

InChI

1S/C15H13NO2/c16-15(17)18-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9H2,(H2,16,17)

InChI key

ZZOKVYOCRSMTSS-UHFFFAOYSA-N

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

新产品

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分析证书(COA)

Lot/Batch Number

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Choi Yi Li et al.
Chembiochem : a European journal of chemical biology, 20(1), 46-50 (2018-09-19)
Urokinase-type plasminogen activator (uPA) and tissue-type plasminogen activator (tPA) are two serine proteases that contribute to initiating fibrinolysis by activating plasminogen. uPA is also an important tumour-associated protease due to its role in extracellular matrix remodelling. Overexpression of uPA has
Simon J de Veer et al.
The Biochemical journal, 469(2), 243-253 (2015-05-20)
Laskowski inhibitors regulate serine proteases by an intriguing mode of action that involves deceiving the protease into synthesizing a peptide bond. Studies exploring naturally occurring Laskowski inhibitors have uncovered several structural features that convey the inhibitor's resistance to hydrolysis and

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