GW9508

This product is for research use only, not for human use. We do not sell to patients.

GW9508
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Size Price Stock
250mg$450Check With Us
500mg$750Check With Us
1g$1125Check With Us

Cat #: V1805 CAS #: 885101-89-3 Purity ≥ 98%

Description: GW9508 is a novel, potent and selective agonist for FFA1 (fatty acid receptor GPR40) with pEC50 of 7.32, and is 100-fold selective against GPR120, it stimulates insulin secretion in a glucose-sensitive manner.

References: Fujita T, et al. A GPR40 agonist GW9508 suppresses CCL5, CCL17, and CXCL10 induction in keratinocytes and attenuates cutaneous immune inflammation. J Invest Dermatol, 2011, 131(8), 1660-1667.

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Molecular Weight (MW)347.41
Molecular FormulaC22H21NO3
CAS No.885101-89-3
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 69 mg/mL (198.6 mM)r
Water: <1 mg/mLr
Ethanol: 69 mg/mL (198.6 mM)
SynonymsGW9508; GW-9508; GW 9508.
ProtocolIn VitroGW9508 inhibits CCL17 and CCL5 expression in pertussis toxin-sensitive cells. The inhibition of GW9508 can be eliminated by depleting GPR40 using RNA interference. GW9508 further inhibits the expression of IL-11, IL-24, and IL-33 induced by TNF-α and IFN-γ in HaCaT cells. GW9508 also inhibits the production of CCL5 and CXCL10 by normal human epidermal keratinocytes
In VivoIn repeated hapten application models (BALB/c and C57BL/6 mice), topical administration of 200 (μM) of GW9508 to the skin inhibits ear swelling and inhibits contact hypersensitivity reactions by downregulating CCL5 and CXCL10, respectively
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM2.8784 mL14.3922 mL28.7844 mL57.5689 mL
5mM0.5757 mL2.8784 mL5.7569 mL11.5138 mL
10mM0.2878 mL1.4392 mL2.8784 mL5.7569 mL
20mM0.1439 mL0.7196 mL1.4392 mL2.8784 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
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.