质量水平
方案
98%
表单
powder
mp
218-220 °C (lit.)
SMILES字符串
O=C1CNC(=O)N1
InChI
1S/C3H4N2O2/c6-2-1-4-3(7)5-2/h1H2,(H2,4,5,6,7)
InChI key
WJRBRSLFGCUECM-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
应用
本产品已被用作底物（在 40℃ 和 pH 9.0 下），以测定红小豆提取物中的 D -海因酶活性。
用于合成以下物质的反应物：
抗癌药物 N-苄基无赖氨酸视蛋白类似物
D-谷氨酸基抑制剂
抗糖尿病铬-2,4-噻唑烷二酮类
具有脑渗透性的GSK-3β抑制剂
作为 15-PGDH 抑制剂的噻唑烷二酮衍生物
放射增敏剂
抗癌药物 N-苄基无赖氨酸视蛋白类似物
D-谷氨酸基抑制剂
抗糖尿病铬-2,4-噻唑烷二酮类
具有脑渗透性的GSK-3β抑制剂
作为 15-PGDH 抑制剂的噻唑烷二酮衍生物
放射增敏剂
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
Eyeshields, Gloves, type N95 (US)
Effect of treatment with compressed CO2 and propane on D-hydantoinase activity
Andrade JM, et al.
Journal of Supercritical Fluids, 46(2), 342-350 (2008)
June Izquierdo et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(53), 12431-12438 (2019-07-19)
A bifunctional amine/squaramide catalyst promoted direct aldol addition of an hydantoin surrogate to pyridine 2-carbaldehyde N-oxides to afford adducts bearing two vicinal tertiary/quaternary carbons in high diastereo- and enantioselectivity (d.r. up to >20:1; ee up to 98 %) is reported. Acid
Lixuan Zhan et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 33(1), 1313-1329 (2018-08-28)
Hypoxic preconditioning (HPC) alleviates the selective and delayed neuronal death in the hippocampal CA1 region induced by transient global cerebral ischemia (tGCI). This type of cell death may include different programmed cell death mechanisms, namely, apoptosis and necroptosis. Although apoptotic
I Hauksson et al.
The British journal of dermatology, 174(2), 371-379 (2015-10-20)
Formaldehyde is a well-known contact sensitizer. Formaldehyde releasers are widely used preservatives in skincare products. It has been found that formaldehyde at concentrations allowed by the European Cosmetics Directive can cause allergic contact dermatitis. However, we still lack information on
Narsimha Reddy Penthala et al.
Bioorganic & medicinal chemistry letters, 21(5), 1411-1413 (2011-02-08)
A series of novel substituted (Z)-5-((1-benzyl-1H-indol-3-yl)methylene)imidazolidin-2,4-diones (3a-f) and (Z)-5-((1-benzyl-1H-indol-3-yl)methylene)-2-iminothiazolidin-4-ones (3g-o) have been synthesized utilizing microwave irradiation. These analogs were evaluated for in vitro cytotoxicity against a panel of 60 human tumor cell lines. Compound 3i exhibits potent growth inhibition against
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持