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
EC Number:
207-652-7
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
157503
MDL number:
InChI key
UYEUUXMDVNYCAM-UHFFFAOYSA-N
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)
SMILES string
Oc1nc(O)c2nccnc2n1
assay
97%
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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
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
Xiaofeng Zhang et al.
Journal of molecular biology, 328(1), 167-182 (2003-04-10)
6,7-Dimethyl-8-ribityllumazine is the biosynthetic precursor of riboflavin, which, as a coenzyme, plays a vital role in the electron transfer process for energy production in all cellular organisms. The enzymes involved in lumazine biosynthesis have been studied in considerable detail. However
M S Ibrahim et al.
Journal of pharmaceutical and biomedical analysis, 28(2), 217-225 (2002-04-04)
The interaction of lumazine, an antibacterial drug, with alpha-, beta-cyclodextrins and DNA in aqueous solution was studied by differential pulse stripping voltammetry and cyclic voltammetry as well as UV-vis spectroscopy. The electrochemical and absorption spectral data indicated a 1:1 complex
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