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Merck
CN

D4893

Sigma-Aldrich

3,4-脱氢-L-脯氨酸

≥98% (TLC), suitable for ligand binding assays

别名:

(S)-3-吡咯啉-2-羧酸, 3,4-二脱氢-L-脯氨酸

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About This Item

经验公式(希尔记法):
C5H7NO2
CAS号:
分子量:
113.11
Beilstein:
5376764
EC 号:
MDL编号:
UNSPSC代码:
12352209
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.26

product name

3,4-脱氢-L-脯氨酸,

检测方案

≥98% (TLC)

质量水平

形式

powder

技术

ligand binding assay: suitable

颜色

white

mp

248-250 °C

应用

peptide synthesis

SMILES字符串

OC(=O)[C@H]1NCC=C1

InChI

1S/C5H7NO2/c7-5(8)4-2-1-3-6-4/h1-2,4,6H,3H2,(H,7,8)/t4-/m0/s1

InChI key

OMGHIGVFLOPEHJ-BYPYZUCNSA-N

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一般描述

3,4-脱氢-L-脯氨酸起脯氨酰-t-RNA合成酶的作用。

生化/生理作用

3,4-脱氢-L-脯氨酸用作各种酶的底物和抑制剂。 3,4-脱氢-L-脯氨酸可用于抑制延伸蛋白的生物合成。 3,4-脱氢-L-脯氨酸是氨基酸氧化酶NikD的替代底物。3,4-脱氢-L-脯氨酸抑制软骨细胞分泌胶原蛋白。

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Chunxiang Xu et al.
BMC plant biology, 11, 38-38 (2011-02-26)
Hydroxyproline rich glycoproteins (HRGPs) are implicated to have a role in many aspects of plant growth and development but there is limited knowledge about their localization and function during somatic embryogenesis of higher plants. In this study, the localization and
Acute respiratory failure (1985)
J B Cooper et al.
Plant physiology, 104(2), 747-752 (1994-02-01)
We investigated the function of cell wall hydroxyproline-rich glycoproteins by observing the effects of a selective inhibitor of prolyl hydroxylase, 3,4-dehydro-L-proline (Dhp), on wall regeneration by Nicotiana tabacum mesophyll cell protoplasts. Protoplasts treated with micromolar concentrations of Dhp do not
T A Sullivan et al.
The Journal of biological chemistry, 269(36), 22500-22506 (1994-09-09)
During development and fracture repair, endochondral bone formation is preceded by an orderly process of chondrocyte hypertrophy and cartilage matrix calcification. Analysis of calcifying versus noncalcifying cartilage has identified several differences in matrix proteins; among these are appearance of a
Andrew G Mark et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 12(8), 1474-1480 (2011-04-28)
The expression of chirality at surfaces, arising from the adsorption of chiral molecules, is usually discussed in terms of the molecular handedness. However, the adsorption process often leads to a new manifestation of chirality in the form of the adsorption

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