跳转至内容
Merck
CN

93834

2-Chloro-4-nitrophenyl-α-D-maltotrioside

chromogenic, ≥95% (HPLC), powder or crystals

别名:

2-chloro-4-nitrophenyl O-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranosyl-(1→4)-α-D-glucopyranoside, CNP-G3

登录 查看组织和合同定价。

选择尺寸


关于此项目

经验公式(希尔记法):
C24H34ClNO18
化学文摘社编号:
分子量:
659.98
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.32
MDL number:
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

2-Chloro-4-nitrophenyl-α-D-maltotrioside, ≥95% (HPLC)

SMILES string

OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O[C@@H]2CO)O[C@H]3[C@H](O)[C@@H](O)[C@H](O[C@@H]3CO)Oc4ccc(cc4Cl)[N+]([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C24H34ClNO18/c25-8-3-7(26(37)38)1-2-9(8)39-22-18(35)15(32)20(11(5-28)41-22)44-24-19(36)16(33)21(12(6-29)42-24)43-23-17(34)14(31)13(30)10(4-27)40-23/h1-3,10-24,27-36H,4-6H2/t10-,11-,12-,13-,14+,15-,16-,17-,18-,19-,20-,21-,22+,23-,24-/m1/s1

InChI key

KMYYNUOXSFGLNX-XFNLHOCBSA-N

assay

≥95% (HPLC)

form

powder or crystals

storage temp.

−20°C

Quality Level

Application

2-Chloro-4-nitrophenyl-α-D-maltotrioside has been used as a substrate in assays to determine the enzymatic activity of α-amylase.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

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

涉药品监管产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Kinetic determination of amylase on microtiter plates: an improved substrate.
J Laine et al.
Pancreas, 13(2), 217-217 (1996-08-01)
alpha-Amylase and alpha-glucosidase inhibitory saponins from Polyscias fruticosa leaves
Hanh TTH, et al.
Journal of Chemistry (2016)
E S Winn-Deen et al.
Clinical chemistry, 34(10), 2005-2008 (1988-10-01)
We describe a direct colorimetric assay for alpha-amylase, with 2-chloro-4-nitrophenyl-alpha-maltotrioside as substrate. Both human pancreatic and salivary amylase split this substrate without the use of helper enzymes, yielding free 2-chloro-4-nitrophenol, which is monitored at 405 nm. The performance of this
A Y Foo et al.
Clinica chimica acta; international journal of clinical chemistry, 272(2), 137-147 (1998-06-26)
The use of 2-chloro-4-nitrophenyl maltotrioside (CNP-G3) as substrate to measure amylase (EC 3.2.1.1) activity in serum directly without the use of auxiliary enzymes was evaluated at two centres. The method was precise (within-run C.V. < 2% and between-run C.V. <
T Suganuma et al.
Carbohydrate research, 303(2), 219-227 (1997-11-14)
The degradation mechanism of a synthetic substrate, 2-chloro-4-nitrophenyl alpha-maltotrioside (CNP-G3), by human salivary alpha-amylase (HSA) was investigated by kinetic and product analyses. It was observed that the enzyme attacked the various CNP-maltooligosaccharides (CNP-G3 to CNP-G6) releasing free CNP. Addition of

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持