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Key Documents

M7684

Sigma-Aldrich

MRS 2159

>98% (HPLC), solid

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About This Item

Empirical Formula (Hill Notation):
C15H11N3O8PNa3
CAS Number:
Molecular Weight:
461.21
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

Assay

>98% (HPLC)

form

solid

solubility

H2O: >10 mg/mL

storage temp.

2-8°C

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

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

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 Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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