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Merck

860166

Sigma-Aldrich

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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About This Item

经验公式(希尔记法):
C4H6N2O3
CAS号:
分子量:
130.10
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

95%

形狀

solid

mp

184-186 °C (dec.) (lit.)

官能基

carboxylic acid

SMILES 字串

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 密鑰

KZKRPYCBSZIQKN-UHFFFAOYSA-N

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應用

Reactant for synthesis of human BACE-1 inhibitors

Additive for crystal nucleation and growth

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析证书(COA)

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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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