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重要文件

H4021

Sigma-Aldrich

D-高丝氨酸

≥98% (TLC)

同義詞:

(R)-(+)-2-氨基-4-羟基丁酸

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About This Item

線性公式:
HOCH2CH2CH(NH2)CO2H
CAS號碼:
分子量::
119.12
Beilstein:
1721680
MDL號碼:
分類程式碼代碼:
12352209
PubChem物質ID:
NACRES:
NA.26
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產品名稱

D-高丝氨酸,

化驗

≥98% (TLC)

品質等級

形狀

powder

顏色

white

mp

205 °C (dec.) (lit.)

應用

peptide synthesis

SMILES 字串

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

InChI

1S/C4H9NO3/c5-3(1-2-6)4(7)8/h3,6H,1-2,5H2,(H,7,8)/t3-/m1/s1

InChI 密鑰

UKAUYVFTDYCKQA-GSVOUGTGSA-N

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生化/生理作用

D-Homoserine is used for the synthesis of bacterial polysaccharids such as the O-antigen of Acinetobacter lwoffii EK30A. D-Homoserine is used to produce atypical serine protease(s) for mechanism studies.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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分析證明 (COA)

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Nikolay P Arbatsky et al.
Organic & biomolecular chemistry, 8(15), 3571-3577 (2010-06-12)
We established a peculiar structure of the O-specific polysaccharide (O-antigen) of a psychrotrophic strain of Acinetobacter lwoffii, EK30A, isolated from a 1.6-1.8 million-year-old Siberian permafrost subsoil sediment sample. The polysaccharide was released by mild acid degradation of the lipopolysaccharide and
Subhash C Annedi et al.
Bioorganic & medicinal chemistry, 14(1), 214-236 (2005-10-04)
The mechanism of proteolysis by serine proteases is a reasonably well-understood process. Typically, a histidine residue acting as a general base deprotonates the catalytic serine residue and the hydrolytic water molecule. We disclose here, the use of an unnatural d-amino
Kimiyasu Isobe et al.
Enzyme research, 2010, 567210-567210 (2010-11-05)
A simple enzymatic method for production of a wide variety of D-amino acids was developed by kinetic resolution of DL-amino acids using L-amino acid oxidase (L-AAO) with broad substrate specificity from Rhodococcus sp. AIU Z-35-1. The optimum pH of the

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