C13408
O -（羧甲基）羟胺 半盐酸盐
98%
别名:
羧甲氧基胺半盐酸盐, (氨氧基)乙酸 半盐酸盐, (羧基甲氧基)胺 半盐酸盐, 羟胺-O-乙酸 半盐酸盐
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关于此项目
线性分子式:
NH2OCH2COOH · 0.5HCl
化学文摘社编号:
分子量:
109.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-862-3
Beilstein/REAXYS Number:
3680528
MDL number:
biological source
synthetic (organic)
Quality Level
assay
98%
form
crystalline powder, powder or crystals
mp
156 °C (dec.) (lit.)
solubility
water: 100 mg/mL, clear to slightly hazy, colorless to faintly yellow
storage temp.
2-8°C
SMILES string
Cl.NOCC(O)=O.NOCC(O)=O
InChI
1S/2C2H5NO3.ClH/c2*3-6-1-2(4)5;/h2*1,3H2,(H,4,5);1H
InChI key
KBXIJIPYZKPDRU-UHFFFAOYSA-N
Application
O-(羧甲基)羟胺半盐酸盐可作为反应物通过与醛和酮缩合合成肟。它还可作为(吡哆醛 5’-磷酸) PLP-依赖性 β-裂解酶的有效抑制剂。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
商品
本文介绍了增殖活性细胞为何需要碳源和氮源合成大分子。尽管大部分肿瘤细胞利用有氧糖酵解途径并分流线粒体氧化磷酸化代谢物，但许多肿瘤细胞表现出线粒体活性增加。
Sigma article discusses tumor cell metabolic pathways, focusing on aerobic glycolysis and mitochondrial activity.
A Sala et al.
Farmaco (Societa chimica italiana : 1989), 46(7-8), 887-897 (1991-07-01)
The synthesis of new 2-(3-bromo-5-isoxazolylideneamino-oxy)acetic acids and their condensation derivatives with suitable beta-lactam nuclei is reported. Their antibacterial properties have been tested in vitro. An interesting activity against Gram-positive bacteria including beta-lactamase-producing microorganisms was found among the cephalosporanic acid derivatives.
Tetrahedron Letters, 34, 4347-4347 (1993)
Characterization of a 5'-aldehyde terminus resulting from the oxidative attack at C5 `of a 2-deoxyribose on DNA
Angeloff A, et al.
Chemical Research in Toxicology, 14, 1413-1420 (2001)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| C13408-10G | 04061833467367 |
| C13408-1G | 04061833467374 |
| C13408-25G | 04061832104959 |