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Ваноксерин дигидрохлорид

Ваноксерин дигидрохлорид структура
67469-78-7
CAS №
67469-78-7
Химическое название:
Ваноксерин дигидрохлорид
английское имя:
Vanoxerine dihydrochloride
Синонимы:
I-893;GBR 12909;Vanoxerine;Boxeprazine;GBR129092HCl;Vanoxerine 2HCl;Inhibitor of DAT;vanoxerine-GBR-12909;I893 dihydrochloride;GBR 12909 DIHYDROCHLORIDE
CBNumber:
CB9398144
Формула:
C28H33ClF2N2O
молекулярный вес:
487.03
MOL File:
67469-78-7.mol

Ваноксерин дигидрохлорид атрибут

Температура плавления: 221 °C
температура хранения: Sealed in dry,Room Temperature
растворимость: ДМСО: свежеприготовленные растворы >5 мг/мл ежедневно
форма: Твердый
цвет: белый
Растворимость в воде: Растворим в ДМСО до 50 мМ. Растворим до 5 мМ в воде при нагревании.
Стабильность:: Растворы в ДМСО или дистиллированной воде можно хранить при температуре -20° до 1 месяца.
FDA UNII: MWO1IP03EV

Заявления о рисках и безопасности

WGK Германия 3
кода HS 2933.59.5300

Ваноксерин дигидрохлорид химические свойства, назначение, производство

Описание

Vanoxerine dihydrochloride (GBR-12909 dihydrochloride) is a potent inhibitor that blocks dopamine uptake (IC50 = 1-51 nM). It is more than 100-fold less effective at blocking serotonin or noradrenaline uptake. GBR 12909 effectively inhibits dopamine uptake in vivo, leading to consequent stimulation of dopamine receptors. GBR 12909 also inhibits pyrilamine binding to the histamine H1 receptor (IC50 = 18 nM) but poorly inhibits ligand binding to dopamine, adrenergic, acetylcholine, serotonin, and γ-aminobutyric acid receptors. It also blocks ligand binding to sigma receptors in rat brain (IC50 = 48 nM).

Использование

Vanoxerine dihydrochloride is a Dopamine reuptake inhibitor that is developed for treatment of Parkinson's disease and depression but has no effect on these diseases.

Определение

ChEBI: Vanoxerine dihydrochloride is a hydrochloride salt that is obtained by reaction of vanoxerine with two equivalents of hydrogen chloride. Potent, competitive inhibitor of dopamine uptake (Ki = 1 nM for inhibition of striatal dopamine uptake). Has > 100-fold lower affinity for the noradrenalin and 5-HT uptake carriers. Also a potent sigma ligand (IC50 = 48 nM). Centrally active following systemic administration. It has a role as a dopamine uptake inhibitor. It contains a vanoxerine(2+).

Общее описание

Vanoxerine dihydrochloride is a potent inhibitor of dopamine active transporter (DAT, Ki = 1 nM, IC50 = 40 and 51 nM) with >100 fold selectivity over noradrenalin and 5-HT re-uptake transporter. Shown to produce behavioral profile in mice for bipolar mania disease model and ADHD disease models.

Опасность

A poison.

Биологическая активность

Potent, competitive inhibitor of dopamine uptake (K i = 1 nM for inhibition of striatal dopamine uptake). Has > 100-fold lower affinity for the noradrenalin and 5-HT uptake carriers. Also a potent sigma ligand (IC 50 = 48 nM). Centrally active following systemic administration.

Ваноксерин дигидрохлорид препаратная продукция и сырье

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Ваноксерин дигидрохлорид поставщик

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