物质信息

ID:354797

3-异丁基-1-甲基黄嘌呤

名称和标识
别名
1-甲基-3-异丁基黄嘌呤3,7-二氢-1-甲基-3-(2-甲基丙基)-1H-嘌呤-2,6-二酮3-异丁基-1-甲基黄嘌呤3-异丁基-1-甲基-2,6(1H,3H)-嘌呤二酮3-Isobutyl-1-methylxanthineIBMX1-Methyl-3-isobutylxanthine3-Isobutyl-1-methyl-2,6(1H,3H)-purinedione3,7-Dihydro-1-methyl-3-(2-methylpropyl)-1H-purine-2,6-dione
IUPAC传统名
3 isobutyl 1 methylxanthine
IUPAC标准名
1-methyl-3-(2-methylpropyl)-2,3,6,7-tetrahydro-1H-purine-2,6-dione
数据登录号
Beilstein号
化合物性质
产品相关信息
纯度
≥98.0% (HPLC)
Empirical Formula (Hill Notation)
C10H14N4O2
级别
purum
安全信息
GHS危险声明
H302
MSDS下载
GHS警示词
Warning
GHS危险品标识
GHS07
急性毒性(口服,皮肤接触,吸入),类别4
皮肤刺激,类别2
眼刺激,类别2
皮肤过敏,类别1
特定目标器官毒性 -一次接触,类别3
欧盟危险性物质标志
有害性 有害性 (Xn)
RTECS编号
ZD8500000
危险公开号
22
个人保护装置
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
德国WGK号
3
理化性质
熔点
201-203 °C
200-201 °C(lit.)
描述信息
Other Notes
Raises intracellular cyclic AMP levels2; Produces partial inhibition of cAMP-phosphodiesterase3
Biochem/physiol Actions
Non-specific inhibitor of cAMP and cGMP phosphodiesterases. The increase in cAMP level as a result of phosphodiesterase inhibition by IBMX activates PKA leading to decreased proliferation, increased differentiation, and induction of apoptosis. IBMX inhibits phenylephrine-induced release of 5-hydroxytryptamine from neuroendocrine epithelial cells of the airway mucosa (IC50: 1.3 μM). Also serves as an adenosine receptor antagonist. Shown to inhibit ion channels in the neuromuscular junction, GH3 cells, and vascular smooth muscle cells. Induces calcium release from intracellular stores in sensory neurons.1
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