Merck
CN
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文件

69720

Sigma-Aldrich

1-甲基黄嘌呤

≥97.0% (HPLC)

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别名:
2,6-二羟基-1-甲基嘌呤
经验公式（希尔记法）:
C6H6N4O2
CAS号:
6136-37-4
分子量:
166.14
Beilstein:
171507
EC 号:
228-108-5
MDL编号:
MFCD00005561
PubChem化学物质编号:
57652204
NACRES:
NA.22

检测方案

≥97.0% (HPLC)

形式

powder

mp

≥300 °C

SMILES string

CN1C(=O)Nc2nc[nH]c2C1=O

InChI

1S/C6H6N4O2/c1-10-5(11)3-4(8-2-7-3)9-6(10)12/h2H,1H3,(H,7,8)(H,9,12)

InChI key

MVOYJPOZRLFTCP-UHFFFAOYSA-N

Gene Information

rat ... Adora1(29290) , Adora2a(25369)

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包装

无底玻璃瓶。内含物装在插入的融合锥内。

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说明
价格

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

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Catherine M Wheatley et al.
American journal of physiology. Endocrinology and metabolism, 287(4), E804-E809 (2004-06-24)
Exercise and insulin increase muscle glucose uptake by different mechanisms and also increase capillary recruitment, which is proposed to facilitate access for hormones and nutrients. The genetically obese Zucker rat shows impaired insulin- but not contraction-mediated glucose uptake in muscle.
Stephen Rattigan et al.
Exercise and sport sciences reviews, 33(1), 43-48 (2005-01-11)
Blood flow to contracting muscles is increased rapidly and is redistributed within the muscle. Recent research has highlighted that insulin causes similar changes, but these are absent in insulin resistance, resulting in impaired insulin-mediated muscle glucose uptake. Understanding the mechanisms
Seong-Yun Jeong et al.
International journal of pharmaceutics, 372(1-2), 132-139 (2009-01-27)
Most of methylxanthine derivatives including caffeine have been known to radiosensitize cancer cells, but the obstacles such as toxicity, request of high dose and poor solubility hinder their preclinical evaluations and clinical applications. In this study, we evaluated the efficacy
Hermann M Bolt et al.
Archives of toxicology, 79(4), 196-200 (2004-11-24)
A comparative study of N-acetyltransferase 2 (NAT2) genotyping and phenotyping (caffeine test method) was performed on 211 persons to elucidate apparent discrepancies in the assignment of NAT2*12 and NAT2*13 alleles which occur in the literature. The study used the standard
Hideo Nakabayashi et al.
BioFactors (Oxford, England), 34(4), 293-302 (2008-01-01)
To understand the mechanisms of the anti-obesity effects of dietary caffeine, the effects of caffeine and its metabolites on adipocyte differentiation and insulin-stimulated glucose uptake in murine 3T3-L1 adipocytes were investigated. Caffeine did not inhibit the differentiation of 3T3-L1 pre-adipocytes
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