An antagonist of REV-ERBα
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SR8278

Item No. 17000

Technical Information
Formal Name
1,2,3,4-tetrahydro-2-[[5-(methylthio)-2-thienyl]carbonyl]-3-isoquinolinecarboxylic acid, ethyl ester
CAS Number
1254944-66-5
Molecular Formula
C18H19NO3S2
Formula Weight
Purity
≥90%
Formulation
A crystalline solid
DMF: 15 mg/mlDMSO: 10 mg/mlEthanol: 15 mg/mlEthanol:PBS (pH 7.2) (1:2): 0.3 mg/ml
λmax
248, 309 nm
SMILES
O=C(OCC)C1N(C(C2=CC=C(SC)S2)=O)CC3=CC=CC=C3C1
InChi Code
InChI=1S/C18H19NO3S2/c1-3-22-18(21)14-10-12-6-4-5-7-13(12)11-19(14)17(20)15-8-9-16(23-2)24-15/h4-9,14H,3,10-11H2,1-2H3
InChi Key
UIEBLUZPSFAFOC-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    OBESITY RESEARCH SOLUTIONS
    Product Description

    REV-ERBα is a nuclear receptor and transcription repressor that coordinates circadian rhythm and metabolic pathways in a heme-dependent manner.1,2 SR8278 is an antagonist of REV-ERBα (EC50 = 0.47 µM), blocking activation of the receptor by the synthetic agonist GSK 4112 (Item No. 11931).2 Moreover, SR8278 stimulates the expression of two REV-ERBα target genes involved in the regulation of glucose production, glucose 6-phosphatase and phosphoenolpyruvate carboxykinase, in liver cells.2 SR8278 has been used, with GSK 4112, to elucidate the role of REV-ERBα in regulating glucagon secretion in pancreatic alpha cells.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Duez, H., and Staels, B. Rev-erb-α: An integrator of circadian rhythms and metabolism. J. Appl. Physiol. (1985) 107(6), 1972-1980 (2009).

    2. Kojetin, D., Wang, Y., Kameneck, T.M., et alIdentification of SR8278, a synthetic antagonist of the nuclear heme receptor REV-ERB. ACS Chem. Biol. 6(2), 131-134 (2011).

    3. Vieira, E., Marroquí, L., Figueroa, A.L., et alInvolvement of the clock gene Rev-erb alpha in the regulation of glucagon secretion in pancreatic alpha-cells. PLoS One 8(7), 1-15 (2013).