69723
7-甲基黄嘌呤
≥98.0% (HPLC)
别名:
2,6-二羟基-7-甲基嘌呤, 杂黄质
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关于此项目
经验公式（希尔记法）:
C6H6N4O2
化学文摘社编号:
分子量:
166.14
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-019-0
Beilstein/REAXYS Number:
171027
MDL number:
Assay:
≥98.0% (HPLC)
Form:
powder
InChI key
PFWLFWPASULGAN-UHFFFAOYSA-N
InChI
1S/C6H6N4O2/c1-10-2-7-4-3(10)5(11)9-6(12)8-4/h2H,1H3,(H2,8,9,11,12)
SMILES string
Cn1cnc2NC(=O)NC(=O)c12
assay
≥98.0% (HPLC)
form
powder
mp
≥300 °C
Gene Information
rat ... Adora1(29290), Adora2a(25369)
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General description
7-甲基黄嘌呤是一种氧代嘌呤，属于黄嘌呤类。它可以由4-氨基-1-甲基咪唑-5-甲酰胺与碳酸二乙酯反应合成。
Application
7-甲基黄嘌呤可用作合成三环咪唑并[2,1-i]嘌呤酮类衍生物的结构单元，作为潜在的腺苷受体拮抗剂。
Packaging
无底玻璃瓶。内含物装在插入的融合锥内。
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
K Trier et al.
The British journal of ophthalmology, 83(12), 1370-1375 (1999-11-27)
To examine a possible effect of 7-methylxanthine, theobromine, acetazolamide, or L-ornithine on the ultrastructure and biochemical composition of rabbit sclera. Groups of pigmented rabbits, six in each group, were dosed during 10 weeks with one of the substances under investigation
Swati Sucharita Dash et al.
Current microbiology, 55(1), 56-60 (2007-06-08)
In this study, the kinetics of degradation of caffeine and related methylxanthines by induced cells of Pseudomonas sp. was performed. The kinetics data showed that degradation of caffeine, theobromine, and 7-methylxanthine followed Michealis-Menten kinetics. The values of K (m) are
W A Tramontano et al.
Phytochemistry, 29(1), 31-33 (1990-01-01)
The use of a DNA alkylating agent, which induces poly(ADP-ribose) formation, has been employed to study the incorporation of [adenine 14C]NAD into pea root meristem nuclei, which is a prerequisite for poly(ADP-ribose) synthesis. The incorporation of [adenine 14C]NAD is significantly
Imidazo [2, 1-i] purin-5-ones and related tricyclic water-soluble purine derivatives: potent A2A-and A3-adenosine receptor antagonists
Muller CE, et al.
Journal of Medicinal Chemistry, 45(16), 3440-3450 (2002)
Kouichi Mizuno et al.
FEBS letters, 534(1-3), 75-81 (2003-01-16)
In coffee and tea plants, caffeine is synthesized from xanthosine via a pathway that includes three methylation steps. We report the isolation of a bifunctional coffee caffeine synthase (CCS1) clone from coffee endosperm by reverse transcription-polymerase chain reaction (RT-PCR) and
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