>>Signaling Pathways>> Membrane Transporter/Ion Channel>> Calcium Channel>>JTV-519 hemifumarate

JTV-519 hemifumarate (Synonyms: K201 hemifumarate)

Catalog No.GC64004

JTV-519 헤미푸마레이트(K201 헤미푸마레이트)는 근형질 세망 Ca2+-자극 ATPase(SERCA)의 Ca2+-의존성 차단제이며 줄무늬 근육의 리아노딘 수용체의 부분 작용제입니다.

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JTV-519 hemifumarate Chemical Structure

Cas No.: 1435938-25-2

Size 가격 재고 수량
1 mg
US$270.00
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

JTV-519 hemifumarate (K201 hemifumarate) is a Ca2+-dependent blocker of sarcoplasmic reticulum Ca2+-stimulated ATPase (SERCA) and a partial agonist of ryanodine receptors in striated muscle. Antiarrhythmic and cardioprotective properties[1][2].

JTV-519 (K201) inhibits inward Ca2+ movement into large unilamellar vesicles (LUV) caused by annexin V in a dose-dependent manner. In the presence of 50 nM annexin V and 400 μM Ca2+, 3 μM JTV-519 shows significant inhibition of Ca2+ movement due to annexin V, and 50% inhibition is achieved at 25 μM K201[2].

JTV-519 (0.5mg/kg/h, i.v., 2 h before the surgery) improves cardiac function in CLP mice, where the fractional shortening (FS) and ejection fraction (EF) are significantly increased as compared with CLP mice without JTV-519 treatment[3].

[1]. Darcy YL, et al. K201 (JTV519) is a Ca2+-Dependent Blocker of SERCA and a Partial Agonist of Ryanodine Receptors in Striated Muscle. Mol Pharmacol. 2016 Aug;90(2):106-15.
[2]. Kaneko N, et al. Inhibition of annexin V-dependent Ca2+ movement in large unilamellar vesicles by K201, a new 1,4-benzothiazepine derivative. Biochim Biophys Acta. 1997 Nov 13;1330(1):1-7.
[3]. Yang J, et al. Toll-like receptor 4-induced ryanodine receptor 2 oxidation and sarcoplasmic reticulum Ca2+ leakage promote cardiac contractile dysfunction in sepsis. J Biol Chem. 2018 Jan 19;293(3):794-807.

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