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Merck
CN

860166

2-咪唑啉酮-4-羧酸

95%

别名:

2-氧代-4-咪唑烷酮-羧酸

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关于此项目

经验公式(希尔记法):
C4H6N2O3
化学文摘社编号:
分子量:
130.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
Form:
solid
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InChI key

KZKRPYCBSZIQKN-UHFFFAOYSA-N

SMILES string

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)

assay

95%

form

solid

mp

184-186 °C (dec.) (lit.)

functional group

carboxylic acid

Quality Level

Application

Reactant for synthesis of human BACE-1 inhibitors

Additive for crystal nucleation and growth

wgk

WGK 3

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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