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AH 7614

SKU: orb1217792

Description

AH 7614 is a selective and potent free fatty acid receptor 4 (FFA4/GPR120) antagonist.

Images & Validation

Key Properties

CAS Number6326-06-3
MW351.42
Purity>98% (HPLC)
FormulaC20H17NO3S
SMILESO=S(C1=CC=C(C)C=C1)(NC2C3=C(OC4=C2C=CC=C4)C=CC=C3)=O
TargetGPR
SolubilityDMSO:35.1 mg/mL(100 mM);Ethanol:Insoluble;Water:Insoluble

Bioactivity

In Vivo
AH7614 (50μg; intratumoral injection once every 4 d for 20 d) reduces the tumor growth in mice. AH7614 (50μg; intratumoral injection one day prior to epirubicin injection) enhances cancer cell sensitivity to the chemotherapy and inhibit tumor progression by blocking GPR120 signaling in combination with Epirubicin.
In Vitro
AH-7614 (compound 39) (0.063-1 μM) blocks intracellular Ca2+ response induced by both linoleic acid and FFAR4 agonist in FFA4 expressing U2OS cells. AH-7614 (100 μM) abolishes the enhancement in glucose-stimulated insulin secretion by GSK137647A in NCI-H716 cells. AH-7614 (0.001-10 μM; 15 min) blocks TUG-891-mediated internalization of FFA4 from the cell surface (pIC50= 7.70). AH-7614 (10 μM; 30 min) blocks agonist-induced elevation of intracellular inositol monophosphates and phosphorylation of FFA4.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

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  • AH-7614 [orb1306116]

    99.91%

    6326-06-3

    351.42

    C20H17NO3S

    5 mg, 10 mg, 25 mg, 100 mg, 200 mg, 1 ml x 10 mM (in DMSO), 2 mg, 50 mg
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Protocol Information

AH 7614 (orb1217792)

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Available Sizes

Select a size below

5 mg
$ 90.00
10 mg
$ 140.00
25 mg
$ 270.00
50 mg
$ 450.00
100 mg
$ 600.00
200 mg
$ 770.00
500 mg
$ 990.00