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About This Item
Empirical Formula (Hill Notation):
C10H12Li3N5O9P2S
CAS Number:
Molecular Weight:
461.07
UNSPSC Code:
41106305
eCl@ss:
32160414
PubChem Substance ID:
NACRES:
NA.77
MDL number:
Assay:
≥80% (HPLC)
Form:
powder
Product Name
Adenosine 5′-[β-thio]diphosphate trilithium salt, ≥80% (HPLC)
Quality Segment
assay
≥80% (HPLC)
form
powder
storage temp.
−20°C
SMILES string
[Li+].[Li+].[Li+].Nc1ncnc2n(cnc12)[C@@H]3O[C@H](COP([O-])(=O)OP([O-])([O-])=S)[C@@H](O)[C@H]3O
InChI
1S/C10H15N5O9P2S.3Li/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(23-10)1-22-25(18,19)24-26(20,21)27;;;/h2-4,6-7,10,16-17H,1H2,(H,18,19)(H2,11,12,13)(H2,20,21,27);;;/q;3*+1/p-3/t4-,6-,7-,10-;;;/m1.../s1
InChI key
CPKFUAYUUSSFFZ-MSQVLRTGSA-K
General description
Substrate and inhibitor for AMP dependent enzyme systems.
Application
Adenosine 5′-[β-thio]diphosphate is a substrate and inhibitor for AMP dependent enzyme systems. Adenosine 5′-[β-thio]diphosphate has been used to explore the myenteric control mechanisms of human esophageal motility and the effect of nitrergic and nonnitrergic neurotransmitters.
Adenosine 5′-[β-thio]diphosphate trilithium salt has been used to induce neuropathic pain in rats to study the effect of dorsal horn cannabinoid CB2 receptor activation on the expression of P2Y12 and P2Y13 (purinoceptors) receptors.
Biochem/physiol Actions
P2Y receptor agonist.
Features and Benefits
This compound is featured on the P2 Receptors: P2Y G-Protein Family page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
Other Notes
Non-hydrolyzable ADP analog
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - STOT SE 2
target_organs
Eyes,Central nervous system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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