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About This Item
经验公式（希尔记法）:
C15H11N3O8PNa3
CAS号:
分子量:
461.21
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77
推荐产品
化驗
>98% (HPLC)
形狀
solid
溶解度
H2O: >10 mg/mL
儲存溫度
2-8°C
SMILES 字串
[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 密鑰
VCUDBCPCDKEAKO-GLCFPVLVSA-K
基因資訊
human ... P2RX1(5023)
生化／生理作用
P2X1 purinoceptor antagonist.
特點和優勢
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.
法律資訊
Sold under license from the National Institutes of Health
儲存類別代碼
13 - Non Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
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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