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P1,P5-Di(adenosine-5′) pentaphosphate trilithium salt_分子结构_CAS_75522-97-3)
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P1,P5-Di(adenosine-5′) pentaphosphate trilithium salt

产品号 31583 公司名称 Sigma Aldrich
CAS号 75522-97-3 公司网站 http://www.sigmaaldrich.com
分子式 C20H24Li5N10O22P5 电 话 1-800-521-8956
分子量 946.032165 传 真
纯 度 ≥95% (HPLC) 电子邮件
保 存 Chembase数据库ID: 132413

产品价格信息

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产品别名

标题
P1,P5-Di(adenosine-5′) pentaphosphate trilithium salt
IUPAC标准名
pentalithium(1+) ion ({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphonato}oxy)[({[({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphonato}oxy)phosphinato]oxy}phosphinato)oxy]phosphinate
IUPAC传统名
pentalithium(1+) ion Ap5A
别名
A(5′)P5(5′)A trilithium salt
Diadenosine pentaphosphate trilithium salt

产品登记号

CAS号 75522-97-3
EC号 302-339-2
MDL号 MFCD00044936

产品性质

Empirical Formula (Hill Notation) C20H26Li3N10O22P5
杂质 ≤5% water
纯度 ≥95% (HPLC)
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个人保护装置 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
保存温度 -20°C
德国WGK号 3

产品详细信息

详细说明 (English)
Biochem/physiol Actions
A diadenosine polyphosphate stored in secretory granules of thrombocytes, chromaffin and neuronal cells. After release into the extracellular space, it affects a variety of biological activities in a wide range of target tissues. In the nervous system it acts through various purinergic receptors. It also activates 5′-nucleotidase and inhibits adenosine kinase activity in vitro. Ap5A is metabolized by soluble enzymes in the blood plasma and by membrane-bound ectoenzymes of a number of cell types including endothelial and smooth muscle cells. In cardiac muscle, pM to nM concentrations significantly increase the open-probability of ryanodine-receptor (RyR2) gates, with prolonged action due to slow dissociation from the receptor.1
详细说明 (简体中文)
Biochem/physiol Actions
A diadenosine polyphosphate stored in secretory granules of thrombocytes, chromaffin and neuronal cells. After release into the extracellular space, it affects a variety of biological activities in a wide range of target tissues. In the nervous system it acts through various purinergic receptors. It also activates 5′-nucleotidase and inhibits adenosine kinase activity in vitro. Ap5A is metabolized by soluble enzymes in the blood plasma and by membrane-bound ectoenzymes of a number of cell types including endothelial and smooth muscle cells. In cardiac muscle, pM to nM concentrations significantly increase the open-probability of ryanodine-receptor (RyR2) gates, with prolonged action due to slow dissociation from the receptor.1

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