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About This Item
经验公式（希尔记法）:
C15H11N3O8PNa3
CAS号:
分子量:
461.21
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
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方案
>98% (HPLC)
表单
solid
溶解性
H2O: >10 mg/mL
储存温度
2-8°C
SMILES字符串
[Na+].[Na+].[Na+].[H]C(=O)c1c(O)c(C)nc(\N=N\c2ccc(cc2)C([O-])=O)c1COP([O-])([O-])=O
InChI
1S/C15H14N3O8P.3Na/c1-8-13(20)11(6-19)12(7-26-27(23,24)25)14(16-8)18-17-10-4-2-9(3-5-10)15(21)22;;;/h2-6,20H,7H2,1H3,(H,21,22)(H2,23,24,25);;;/q;3*+1/p-3/b18-17+;;;
InChI key
VCUDBCPCDKEAKO-GLCFPVLVSA-K
基因信息
human ... P2RX1(5023)
生化/生理作用
P2X1 purinoceptor antagonist.
特点和优势
This compound is featured on the P2 Receptors: P2X Ion Channel Family page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
法律信息
Sold under license from the National Institutes of Health
储存分类代码
13 - Non 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
Yong-Chul Kim et al.
Drug development research, 45(2), 52-66 (1998-10-01)
Novel analogs of the P2 receptor antagonist pyridoxal-5'-phosphate-6-phenylazo-2',4'-disulfonate (PPADS) were synthesized. Modifications were made through functional group substitution on the sulfophenyl ring and at the phosphate moiety through the inclusion of phosphonates, demonstrating that a phosphate linkage is not required
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