GW 791343 hydrochloride Chemical Structure
A novel platelet inhibitor
LY404039 is a potent agonist of recombinant human mGlu2, mGlu3 receptors and rat neurons expressing native mGlu2/3 receptors with Ki of 149 nM, 92 nM and 88nM, respectively.
COX-2 inhibitor,IC50=0.04uM
BMS-708163 is a γ-secretase inhibitor (GSI) (IC50 =0.3 nM)
Asenapine is a new atypical antipsychotic used for the treatment of schizophrenia and acute mania associated with bipolar disorder .
Cetirizine Dihydrochloride is an antihistamine.
Etodolac (Lodine) is a COX inhibitor with an IC50 of 53.5 nM.
Etomidate is a GABAA receptors agonist at GABAA receptors.
Flumazenil is a benzodiazepine antagonist.
Fluoxetine is an antidepressant of the selective serotonin reuptake inhibitor (SSRI)class.
GW 791343 hydrochloride is a non-competitive human P2X(7) receptor inhibitor with pIC50 of about 7.1. GW 791343 hydrochloride exhibits negative allosteric effects at the human P2X(7) receptor but is a positive allosteric modulator of the rat P2X(7) receptor. GW 791343 hydrochloride competitively interacted at the ATP binding site and so were probably negative allosteric modulators of the P2X(7) receptor. GW 791343 hydrochloride increased responses to BzATP at the F95L mutant receptor, although the magnitude of this effect was not as marked as at the rat ECD, rat–human or domain 1 receptor. [1][2][3]
| Molecular Weight (WM): | 483.81 |
|---|---|
| Formula: | C20H24F2N4O.3HCl |
| CAS No.: | 309712-55-8 |
| Synonyms: |
N/A
|
| Dissolve in (25°C): | |
| Storage: | 2 years-20°CPowder |
| 1 week-4°Cin DMSO | |
| 1 month-80°in DMSO |
A collection of 864 bioactive compounds
A collection of 481 inhibitors
A collection of 194 kinase inhibitors
A collection of 85 tyrosine kinase inhibitors.
A collection of 426 FDA approved drugs
A collection of 139 natural products
A collection of 40 chemotherapeutic agents
A unique collection of 17 small molecule modulators
A unique collection of 47 small molecule inhibitors
A unique collection of 63 GPCR small molecules
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