L3307
无水茶碱
97%
别名:
2,4(1H,3H)-蝶啶二酮, 2,4-二羟基蝶啶, 2,4-蝶啶二醇
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关于此项目
经验公式（希尔记法）:
C6H4N4O2
化学文摘社编号:
分子量:
164.12
Beilstein:
157503
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
方案
97%
SMILES字符串
Oc1nc(O)c2nccnc2n1
InChI
1S/C6H4N4O2/c11-5-3-4(8-2-1-7-3)9-6(12)10-5/h1-2H,(H2,8,9,10,11,12)
InChI key
UYEUUXMDVNYCAM-UHFFFAOYSA-N
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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)
法规信息
新产品
此项目有
L A Tai et al.
Current medicinal chemistry, 18(1), 69-78 (2010-11-30)
Three xanthine oxidase substrates (i.e., xanthine, adenine, and 2-amino-4-hydroxypterin) show a "substrate inhibition" pattern (i.e., slower turnover rates at higher substrate concentrations), whereas another two substrates (i.e., xanthopterin and lumazine) show a "substrate activation" pattern (i.e., higher turnover rates at
D Jourd'heuil et al.
The Journal of biological chemistry, 276(31), 28799-28805 (2001-05-25)
Peroxynitrite (ONOO(-)/ONOOH), the product of the diffusion-limited reaction of nitric oxide (*NO) with superoxide (O(-*)(2)), has been implicated as an important mediator of tissue injury during conditions associated with enhanced *NO and O(-*)(2) production. Although several groups of investigators have
Sonia B Jiménez-Pulido et al.
Dalton transactions (Cambridge, England : 2003), 42(2), 530-541 (2012-10-23)
The oxime derived from 6-acetyl-1,3,7-trimethyllumazine (1) ((E-6-(hydroxyimino)ethyl)-1,3,7-trimethylpteridine-2,4(1H,3H)-dione, DLMAceMox) has been prepared and its molecular and crystal structure determined from spectral and XRD data. The oxime ligand was reacted with silver nitrate, perchlorate, thiocyanate, trifluoromethylsulfonate and tetrafluoroborate to give complexes with
Mark Cushman et al.
The Journal of organic chemistry, 70(20), 8162-8170 (2005-11-10)
The last two steps in the biosynthesis of riboflavin, an essential metabolite that is involved in electron transport, are catalyzed by lumazine synthase and riboflavin synthase. To obtain structural probes and inhibitors of these two enzymes, two ribityllumazinediones bearing alkyl
Mark Cushman et al.
The Journal of organic chemistry, 67(20), 6871-6877 (2002-10-02)
Several analogues of a hypothetical intermediate in the reaction catalyzed by lumazine synthase were synthesized and tested as inhibitors of both Bacillus subtilis lumazine synthase and Escherichia coli riboflavin synthase. The new compounds were designed by replacement of a two-carbon
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