ChemicalBook

JT010

 структура
917562-33-5
CAS №
917562-33-5
английское имя:
JT010
Синонимы:
JT010;2-Chloro-N-[4-(4-methoxyphenyl)-2-thiazolyl]-N-(3-methoxypropyl)acetamide;2-chloro-N-(4-(4-methoxyphenyl)thiazol-2-yl)-N-(3-methoxypropyl)acetamide;Acetamide, 2-chloro-N-[4-(4-methoxyphenyl)-2-thiazolyl]-N-(3-methoxypropyl)-;JT010,JT-010,TRP Channel,Transient receptor potential channels,inhibit,Inhibitor,JT 010
CBNumber:
CB53386492
Формула:
C16H19ClN2O3S
молекулярный вес:
354.85
MOL File:
917562-33-5.mol

JT010 атрибут

Температура кипения: 487.4±55.0 °C(Predicted)
плотность: 1.265±0.06 g/cm3(Predicted)
температура хранения: 2-8°C
растворимость: ДМСО (Мало растворим), метанол (Мало растворим)
форма: пудра
пка: 2.59±0.10(Predicted)
цвет: От белого до бежевого

Заявления о рисках и безопасности

JT010 химические свойства, назначение, производство

Описание

JT010 is a transient receptor potential ankyrin 1 (TRPA1) agonist (EC50 = 0.65 nM in a calcium influx assay). It is selective for TRPA1 over TRP vanilloid 1 (TRPV1), TRPV3, TRPV4, TRP canonical channel 5 (TRPC5), TRP melastatin 2 (TRPM2), and TRPM8 channels at 1 μM.

Использование

JT010 is a potent and selective TRPA1 channel activator (EC50 = 65 nM); activates the TRPA1 channel by covalently and site-selectively binding to Cys621. Exhibits selectivity for TRPA1 over TRPV1, TRPV3, TRPV4, TRPM2, TRPM8, and TRPC5 channels (EC50 values are >1 μM).

Биохимия/физиол Действия

JT010 is a non-cytotoxic and highly stable (>90% remains after 2 h in 1 mM DTT or 2-mercaptoethanol) chloroacetamido warhead-carrying thiazole derivative that acts as a potent and TRPA1-selective channel activator via covalent modification of TRPA1 active site Cys621. JT0101 stimulates calcium influx in TRPA1-transfected HEK293 cells in a dose-dependent manner (EC50?= 650 pM) with excellent selectivity over TRPV1, TRPV3, TRPV4, TRPM2, TRPM8, and TRPC5 channels (EC50?>1 μM).

JT010 препаратная продукция и сырье

сырьё

препарат


JT010 поставщик

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