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About This Item
经验公式（希尔记法）:
C4H6N2O3
CAS号:
分子量:
130.10
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
检测方案
95%
形式
solid
mp
184-186 °C (dec.) (lit.)
SMILES字符串
OC(=O)C1CNC(=O)N1
InChI
1S/C4H6N2O3/c7-3(8)2-1-5-4(9)6-2/h2H,1H2,(H,7,8)(H2,5,6,9)
InChI key
KZKRPYCBSZIQKN-UHFFFAOYSA-N
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应用
Reactant for synthesis of human BACE-1 inhibitors
Additive for crystal nucleation and growth
Additive for crystal nucleation and growth
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
S Samuels et al.
Pharmacology, biochemistry, and behavior, 24(1), 143-146 (1986-01-01)
DBA/2J mice were exposed in utero, between days 15-18 of gestation, to either of two enzyme inhibitors, previously shown to decrease blood-brain, large-neutral amino acid transport in adults: L-methionine-RS-sulfoximine and 2-imidazolidone-4-carboxylic acid. The young mice demonstrated persistently altered motor behavior
Heuisul Park et al.
Bioorganic & medicinal chemistry letters, 18(9), 2900-2904 (2008-04-25)
We describe synthesis and evaluation of a series of cyclic urea derivatives with hydroxylethylamine isostere. Modification of P3, P1, and P2' and combination of SAR display a >100-fold increase in potency with good cellular activity (IC(50)=0.15microM) relative to the previously
S. Devarakonda, et al.,
Journal of Crystal Growth, 204, 525-538 (1999)
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