M7684
MRS 2159
>98% (HPLC), solid
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About This Item
Empirical Formula (Hill Notation):
C15H11N3O8PNa3
CAS Number:
Molecular Weight:
461.21
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
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+;;;
SMILES string
[Na+].[Na+].[Na+].[H]C(=O)c1c(O)c(C)nc(\N=N\c2ccc(cc2)C([O-])=O)c1COP([O-])([O-])=O
InChI key
VCUDBCPCDKEAKO-GLCFPVLVSA-K
assay
>98% (HPLC)
form
solid
solubility
H2O: >10 mg/mL
storage temp.
2-8°C
Gene Information
human ... P2RX1(5023)
Biochem/physiol Actions
P2X1 purinoceptor antagonist.
Features and Benefits
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.
Legal Information
Sold under license from the National Institutes of Health
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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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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Datasheet
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