GSK269962 HCl
This product is for research use only, not for human use. We do not sell to patients.
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Size | Price | Stock |
---|---|---|
250mg | $1550 | Check With Us |
500mg | $2450 | Check With Us |
1g | $3675 | Check With Us |
Cat #: V3320 CAS #: 2095432-71-4 Purity ≥ 98%
Description: GSK269962 HCl (also called GSK-269962A HCl), the hydrochloride salt of GSK 269962A, is a selective ROCK (Rho-associated protein kinase) inhibitor with potential antihypertensive and cardioprotective activity.
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- Physicochemical and Storage Information
- Protocol
- Related Biological Data
- Stock Solution Preparation
- Quality Control Documentation
Molecular Weight (MW) | 607.07 |
---|---|
Molecular Formula | C29H31ClN8O5 |
CAS No. | 2095432-71-4 |
Storage | -20℃ for 3 years in powder formr |
-80℃ for 2 years in solvent | |
Solubility In Vitro | DMSO: >30 mg/mLr |
Water: N/Ar | |
Ethanol: N/A | |
Solubility In Vivo | N-[3-[[2-(4-amino-1,2,5-oxadiazol-3-yl)-1-ethyl-1H-imidazo[4,5-c]pyridin-6-yl]oxy]phenyl]-4-[2-(4-morpholinyl)ethoxy]-benzamide hydrochloride |
Synonyms | GSK 269962 HCl; GSK-269962 HCl; GSK269962A HCl; GSK 269962A HCl; GSK-269962AHCl;GSK269962B |
Protocol | In Vitro | GSK269962A has an IC50 of 1.6 nM toward recombinant human ROCK1. GSK269962A exhibits more than 30-fold selectivity against a panel of serine/threonine kinases |
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In Vivo | GSK269962A is a potent antihypertensive agent. GSK269962A (0.3, 1, and 3 mg/kg; oral gavage) induces a dose-dependent reduction in blood pressure in spontaneously hypertensive rat (SHR). The reduction of blood pressure is acute and substantial | |
Animal model | Male Sprague-Dawley rats (350-400g) | |
Dosages | 0.3, 1, and 3 mg/kg | |
Administration | Oral gavage; 12 hours |
These protocols are for reference only. InvivoChem does not
independently validate these methods.
Solvent volume to be added | Mass (the weight of a compound) | |||
---|---|---|---|---|
Mother liquor concentration | 1mg | 5mg | 10mg | 20mg |
1mM | 1.6473 mL | 8.2363 mL | 16.4726 mL | 32.9451 mL |
5mM | 0.3295 mL | 1.6473 mL | 3.2945 mL | 6.5890 mL |
10mM | 0.1647 mL | 0.8236 mL | 1.6473 mL | 3.2945 mL |
20mM | 0.0824 mL | 0.4118 mL | 0.8236 mL | 1.6473 mL |
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
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Volume
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Molecular Weight*
The dilution calculator equation
Concentration(start)
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Volume(start)
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Volume(final)
This equation is commonly abbreviated as: C1 V1 = C2 V2
Concentration(start)
C1
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V1
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Step One: Enter information below
Dosage mg/kg
Average weight of animals g
Dosing volume per animal µL
Number of animals
Step Two: Enter the in vivo formulation
%DMSO
+
%
+
%Tween 80
+
%ddH2O
Calculation Results:
Working concentration:
mg/ml;
Method for preparing DMSO master liquid:
mg
drug pre-dissolved in
µL
DMSO(Master liquid concentration
mg/mL)
,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:
Take
µL
DMSO master liquid, next add
µL
PEG300, mix and clarify, next add
µL
Tween 80,mix and clarify, next add
µL
ddH2O,mix and clarify.
Note:
- (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
- (2) Be sure to add the solvent(s) in order.