所有图片(3)
About This Item
经验公式（希尔记法）:
C5H11NO3
CAS号:
分子量:
133.15
Beilstein:
1722350
MDL编号:
UNSPSC代码:
12352209
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.26
推荐产品
产品名称
DL-3-羟基降缬氨酸, ≥98% (TLC)
质量水平
方案
≥98% (TLC)
表单
powder
颜色
white
应用
cell analysis
储存温度
−20°C
SMILES字符串
CCC(O)C(N)C(O)=O
InChI
1S/C5H11NO3/c1-2-3(7)4(6)5(8)9/h3-4,7H,2,6H2,1H3,(H,8,9)
InChI key
LGVJIYCMHMKTPB-UHFFFAOYSA-N
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相关类别
生化/生理作用
3-羟基正缬氨酸（HNV）是一种微生物α氨基酸苏氨酸类似物，具有抗病毒活性（疱疹病毒）并可通过插入到蛋白中而对哺乳动物细胞产生毒性（胚胎毒性和致畸性）。3-羟基正缬氨酸可作为一种非天然氨基酸用于研究在酰基-tRNA编辑水平上蛋白翻译的保真度。3-羟基正缬氨酸也可用于研究苏氨酸代谢中所涉及的酶和分子。
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - 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
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
C Ramos et al.
Applied and environmental microbiology, 58(5), 1677-1682 (1992-05-01)
In this work, we isolated and characterized mutants that overproduce threonine from Saccharomyces cerevisiae. The mutants were selected for resistance to the threonine analog alpha-amino-beta-hydroxynorvalerate (hydroxynorvaline), and, of these, the ones able to excrete threonine to the medium were chosen.
R Louw et al.
Amino acids, 29(3), 207-212 (2005-08-06)
3-Hydroxynorvaline (HNV; 2-amino-3-hydroxypentanoic acid), a microbial L-threonine analogue, is toxic to mammalian cells and displays antiviral properties. In view of this, we investigated the toxicity and/or potential teratogenicity of HNV in developing chicken and mouse embryos. HNV was administered to
R Kumarasamy et al.
Virology, 138(1), 156-161 (1984-10-15)
Treatment of HSV-infected BHK-21 cells with 5-10 mM of beta-hydroxynorvaline (Hnv), an analog of threonine which blocked attachment of oligosaccharides at the Asn-X-Thr sites, markedly inhibited the synthesis of all viral glycoproteins as well as the major capsid protein. However
M J Massare et al.
FEBS letters, 223(1), 122-126 (1987-10-19)
Treatment of HSV-infected cells with 5-10 mM beta-hydroxynorvaline (Hnv), a threonine analog, specifically affects herpesvirus DNA replication: both the rate of and total DNA synthesis are reduced, the former approximately 15-fold by Hnv (6 h post-infection) and the latter by
M M Mareel et al.
Clinical & experimental metastasis, 3(3), 197-207 (1985-07-01)
Inhibitors of glycosylation and carbohydrate processing were used to investigate the role of carbohydrates exposed at the cell surface in invasion. Malignant mouse MO4 cells were confronted with embryonic chick heart in organ culture, an assay shown to be relevant
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