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Merck
CN

A0878

Sigma-Aldrich

丙氨酸甘氨酸

≥99% (TLC)

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别名:
L -丙氨酰-甘氨酸
线性分子式:
CH3CH(NH2)CONHCH2COOH
CAS号:
分子量:
146.14
Beilstein:
1723438
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.26

检测方案

≥99% (TLC)

质量水平

形式

powder

颜色

white

储存温度

−20°C

SMILES字符串

C[C@H](N)C(=O)NCC(O)=O

InChI

1S/C5H10N2O3/c1-3(6)5(10)7-2-4(8)9/h3H,2,6H2,1H3,(H,7,10)(H,8,9)/t3-/m0/s1

InChI key

CXISPYVYMQWFLE-VKHMYHEASA-N

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生化/生理作用

L-丙氨酰甘氨酸是一种简单的营养二肽,也用于氢键和重金属络合等物理化学研究。
丙氨酰二肽,如 ala-leu、ala-lys、ala-gly、ala-pro、ala-tyr 和 ala-phe 可用于理化研究或评价二肽分离技术。丙氨酰二肽也可用于研究细胞摄取机制、二肽代谢或细胞生长补充获益。

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Analysis of vibrational spectra of L-alanylglycine based on density functional theory calculations.
Padmaja L, Ravikumar C, James C, et al.
Spectrochimica Acta Part A: Molecular Spectroscopy, 71, 252-262 (2008)
Masatoshi Watabe et al.
Journal of inorganic biochemistry, 100(10), 1653-1659 (2006-07-22)
We prepared platinum(IV) complexes containing dipeptide and diimine or diamine, the [PtCl(dipeptide-N,N,O)(diimine or diamine)]Cl complex, where -N,N,O means dipeptide coordinated as a tridentate chelate, dipeptide=glycylglycine (NH(2)CH(2)CON(-)CH(2)COO(-), digly, where two protons of dipeptide are detached when the dipeptide coordinates to metal
Puneet Ahuja et al.
Journal of the American Chemical Society, 131(22), 7498-7499 (2009-05-16)
We report the first observation of long-lived states (LLS) having lifetimes T(LLS) that exceed the corresponding spin-lattice relaxation times T(1) by more than a factor 6 in a protein. Slow diffusion coefficients characteristic of large biomolecules can be determined by
Gregory A Barding et al.
Journal of proteome research, 12(2), 898-909 (2012-12-05)
Natural disasters such as drought, extreme temperatures, and flooding can severely impact crop production. Understanding the metabolic response of crops threatened with these disasters provides insights into biological response mechanisms that can influence survival. In this study, a comparative analysis
C J Gray et al.
Biomedical peptides, proteins & nucleic acids : structure, synthesis & biological activity, 2(1), 13-18 (1996-01-01)
The methodology for the incorporation of azaamino-acid residues into peptides synthesised by a solid-phase method has been extended to allow azaalanine peptides to be prepared. In this way, Ac-Leu-Ser-Gly-azaAla-Gly-Phe-Ser-Leu-NH2 H-Ala-Ala-Lys-Glu-Ala-Ala-Glu-Ala -Ala-Glu-Lys-Ala-azaAla-Glu-Leu-Ala-Leu-N2H3, and H-Ala-azaAla-Lys-Glu-Ala-Ala-Glu-Ala-Ala-Glu-Lys-Ala-Ala-Glu-Leu-A la-Leu-N2H3 have been prepared. A new analogue

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