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Merck
CN

92591

Sigma-Aldrich

DL -2,6-二氨基庚二酸

≥95% (TLC)

别名:

rac.-DAP, DL-α,ε-二氨基庚二酸, DL-2,6-二氨基庚二酸

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About This Item

经验公式(希尔记法):
C7H14N2O4
CAS号:
分子量:
190.20
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.25

产品名称

DL -2,6-二氨基庚二酸, ≥95% (TLC)

质量水平

方案

≥95% (TLC)

表单

powder

SMILES字符串

OC([C@@H](N)CCC[C@H](N)C(O)=O)=O

InChI

1S/C7H14N2O4/c8-4(6(10)11)2-1-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)/t4-,5-/m0/s1

InChI key

GMKMEZVLHJARHF-WHFBIAKZSA-N

应用

DL-2,6-二氨基庚二酸是中消旋DAP的立体异构体,可用作用于鉴定反刍动物瘤胃中细菌和真菌标记物的测定的参考材料。

生化/生理作用

内消旋DAP的立体异构体。meso-DAP是许多细菌细胞壁中必需氨基酸L-赖氨酸和肽聚糖成分的生物合成前体。由于在哺乳动物生物化学中未观察到这些功能,因此α,α′-二氨基二酸(DAD)作为具有低哺乳动物毒性的潜在抗生素而受到关注

包装

无底玻璃瓶。内含物装在锥底内插管中。

分析说明

非对映纯度 ≥98.0% (HPLC)

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The DAP pathway to lysine as a target for antimicrobial agents.
R J Cox
Natural product reports, 13(1), 29-43 (1996-02-01)
Yea Hwang Moon et al.
Animal science journal = Nihon chikusan Gakkaiho, 81(6), 642-647 (2010-11-27)
A comparative study among Korean native cow (Hanwoo), Holstein dairy cow, Korean native goat and crossbred sheep on the population and marker concentration of ruminal microbes, the activities of carboxymethylcellulase (CMCase), xylanase and amylase, and in situ dry matter (DM)
J McKerrow et al.
Letters in applied microbiology, 30(3), 178-182 (2000-04-04)
A simple and sensitive method for separating and detecting the LL, DD and meso diastereomers of the dibasic amino acid diaminopimelic acid (DAP) in the peptidoglycan of Gram-positive bacteria is described. This method is based on reverse phase HPLC separation
Diaminopimelate and lysine.
Patte, J. C.
Amino Acids: Biosynthesis and Genetic Regulation, 3, 213-228 (1983)
Zhaoxian Xu et al.
Scientific reports, 5, 17400-17400 (2015-12-04)
Poly(L-diaminopropionic acid) (PDAP) is one of the four homopoly(amino acid)s that have been discovered in nature. However, the molecular mechanism of PDAP biosynthesis has yet to be described. In this work, the general layout of the PDAP biosynthetic pathway is

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