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Амоксапин

Амоксапин структура
14028-44-5
CAS №
14028-44-5
Химическое название:
Амоксапин
английское имя:
Amoxapine
Синонимы:
amoxan;Defanyl;Moxadil;Asendin;Asendis;cl67772;Demolox;Ascendin;CL 67772;AMOXAPINE
CBNumber:
CB5375947
Формула:
C17H16ClN3O
молекулярный вес:
313.78
MOL File:
14028-44-5.mol

Амоксапин атрибут

Температура плавления: 175-1760C
Температура кипения: 469.9±55.0 °C(Predicted)
плотность: 1.2613 (rough estimate)
показатель преломления: 1.5800 (estimate)
Fp: 9℃
температура хранения: Keep in dark place,Inert atmosphere,Room temperature
растворимость: метанол: растворим
форма: Твердый
пка: pKa 7.6 (Uncertain)
цвет: Кристаллы из бензола/петроэфира
Мерк: 14,576
Стабильность:: Stable under recommended storage conditions., Stable Under Recommended Storage C
Справочник по базе данных CAS: 14028-44-5(CAS DataBase Reference)
FDA UNII: R63VQ857OT
Справочник по химии NIST: Amoxapine(14028-44-5)
Предложение 65 Список: Amoxapine
Код УВД: N06AA17
UNSPSC Code: 41116107
NACRES: NA.77
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
Коды опасности Xn
Заявления о рисках 22
Заявления о безопасности 36
РИДАДР 3249
WGK Германия 3
RTECS HQ4025500
Класс опасности 6.1(b)
Группа упаковки III
кода HS 2934990002
Токсичность LD50 in mice (mg/kg): 122 i.p.; 112 orally (Howell, 1972)
символ(GHS) GHS hazard pictograms
сигнальное слово Warning
Заявление об опасности
пароль Заявление об опасности Класс опасности категория сигнальное слово пиктограмма предупреждение
H302 Вредно при проглатывании. Острая токсичность, пероральная Категория 4 Предупреждение GHS hazard pictograms P264, P270, P301+P312, P330, P501
Внимание
P264 После работы тщательно вымыть кожу.
P270 При использовании продукции не курить, не пить, не принимать пищу.
P301+P312 ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии.
P501 Удалить содержимое/ контейнер на утвержденных станциях утилизации отходов.

Амоксапин MSDS


Amoxapine

Амоксапин химические свойства, назначение, производство

Описание

Amoxapine is a tetracyclic antidepressant with a wide range of pharmacological effects. It inhibits norepinephrine and serotonin reuptake, binding the respective transporters with Kd values of 16 and 58 nM. It has also been shown to act as either an antagonist or inverse agonist at serotonin 5-HT2A, 2B, 2C, 3, 6, 7 (Kis = 1 and 2 nM for 5-HT2A and 5-HT2C, respectively), dopamine D2, 3, 4 (Kd = 160 nM for D2), α1-adrenergic (Kd = 50 nM), and histamine H1 (Kd = 25 nM) receptors.

Химические свойства

Crystalline Solid

Использование

Amoxapine is intended more for relieving symptoms in patients with neurotic or situational depression. It has a number of serious side effects.

Определение

ChEBI: A dibenzooxazepine compound having a chloro substituent at the 2-position and a piperazin-1-yl group at the 11-position.

Общее описание

Consideration of the structure of amoxapine, 2-chloro-11-(1-piperazinyl)dibenz-[b,f] [1,4]oxazepine (Asendin), reinforcesthe fact that many antidepressants are very closelyrelated to antipsychotics. Indeed, some, including amoxapine,have significant effects at D2 receptors. The Nmethyl–substituted relative of amoxapine is the antipsychoticloxapine (Loxitane). The 8-hydroxy metabolite ofamoxapine is reportedly active as an antidepressant and asa D2 receptor blocker.

Механизм действия

Additionally, it is the N-desmethyl metabolite of the antipsychotic loxapine. Amoxapine differs structurally from the other secondary TCAs in that it has both a nitrogen and an oxygen atom in its 7-membered central ring and a piperazinyl ring rather than a propylamino side chain attached to the central ring.Amoxapine is a less potent inhibitor of neuronal NE reuptake compared with the other secondary TCAs, with a mechanism of action similar to that of desipramine.

Фармаколо?гия

The antidepressant action of amoxapine is comparable to that of imipramine and amitriptyline. It exhibits antagonistic activity on dopamine (D2) receptors.

Фармакокине?тика

Amoxapine shares the toxic potentials of the TCAs, and the usual precautions of TCA administration should be observed. Amoxapine resembles the atypical antipsychotic drugs in its intermediate affinity as an antagonist of dopamine-2 and of 5-HT2 receptors. Amoxapine is rapidly and almost completely absorbed from the gastrointestinal (GI) tract. Amoxapine and its 8-hydroxyamoxapine metabolite have been detected in human milk at concentrations below steady-state therapeutic concentrations.

Клиническое использование

Amoxapine is a dibenzoxazepine TCA with antidepressant and antipsychotic effects that has shown therapeutic effectiveness in patients with delusional depression.

Профиль безопасности

Poison by ingestion andintraperitoneal routes. Human systemic effects byingestion: acute renal failure, acute tubular necrosis, BPlowering, coma, convulsions, decreased body temperature,EKG changes, excitement, fasciculations, heart ratechanges, hype

Метаболизм

Amoxapine has the shortest elimination time (~8 hours) of the secondary TCAs. It is metabolized in the liver principally to 8-hydroxyamoxapine and to 7-hydroxyamoxapine. Both of these metabolites are pharmacologically active and have half-lives of 30 and 6.5 hours, respectively. The hydroxylation of amoxapine is inhibited by ketoconazole, suggesting the involvement of CYP3A4."

Амоксапин препаратная продукция и сырье

сырьё

препарат


Амоксапин поставщик

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