推荐产品
生物来源
bovine brain
方案
≥98% (TLC)
储存温度
−20°C
SMILES字符串
[K+].O[C@@H]1[C@@H](O)[C@H](OP(O)([O-])=O)[C@H](O)[C@H](O)[C@H]1OP(O)(O)=O
InChI
1S/C6H14O12P2.K/c7-1-2(8)6(18-20(14,15)16)4(10)3(9)5(1)17-19(11,12)13;/h1-10H,(H2,11,12,13)(H2,14,15,16);/q;+1/p-1/t1-,2-,3-,4+,5+,6+;/m1./s1
InChI key
UEZPJWQBOCTMMK-HTBPUPAMSA-M
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生化/生理作用
甘油磷酸肌醇分解生成的磷酸肌醇
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
Molecular and cellular endocrinology, 66(2), 215-229 (1989-10-01)
The optimisation of a reaction for the conversion of glycerophosphoinositols to phosphoinositols is described. This reaction has been used in a scheme, described in detail, for the formation of D-myo-inositol 1,4-bisphosphate and D-myo-inositol 1,4,5-trisphosphate in mg quantities from a readily
The Journal of biological chemistry, 259(5), 3111-3116 (1984-03-10)
The inositol phospholipids of peritoneal macrophages were prelabeled with [3H]inositol to enable studies on the enzymatic mechanisms of stimulus-induced phosphatidylinositol breakdown. Ionophore A23187 induced a rapid breakdown of phosphatidylinositol in the presence of Ca2+ with 25% loss occurring within 5
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