Antazoline hydrochloride
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Antazoline hydrochloride
structure -
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CAS No:
2508-72-7
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Formula:
C17H19N3.ClH
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Chemical Name:
Antazoline hydrochloride
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Synonyms:
1H-Imidazole-2-methanamine,4,5-dihydro-N-phenyl-N-(phenylmethyl)-,hydrochloride (1:1);1H-Imidazole-2-methanamine,4,5-dihydro-N-phenyl-N-(phenylmethyl)-,monohydrochloride;2-Imidazoline,2-[(N-benzylanilino)methyl]-,monohydrochloride;Antazoline hydrochloride;Antistine hydrochloride;2-(N-Benzylanilinomethyl)-2-imidazoline hydrochloride;Phenazoline hydrochloride;Antazoline chloride;Antistina;Antistin;Antastan;Histostab;Antihistal;Imidamine;Azalone;Antasten;Dibistin;5512M;Fenazolina;Histazine;Ben-a-hist
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Categories:
Active Pharmaceutical Ingredients > Circulatory System Drugs
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CAS No:
Description
Antazoline hydrochloride is a 1st generation antihistamine with also anticholinergic properties used to relieve nasal congestion and in eye drops.
An antagonist of histamine H1 receptors.
Antazoline hydrochloride Basic Attributes
301.81
301.134583
219-719-8
FP8Q8F72JH
DTXSID1047782
2933290090
Characteristics
27.6
3.26130
White or almost white crystalline powder
237-241 °C
475.5°C at 760 mmHg
241.4ºC
>45.3 [ug/mL]
Store at RT
3.31E-09mmHg at 25°C
Safety Information
NONH for all modes of transport
3
20/21/22-36/37/38
26-36
NJ2150000
Xn,Xi
P261-P280-P305 + P351 + P338
H302-H312-H315-H319-H332-H335
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 41 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Agents that are used to treat allergic reactions. Most of these drugs act by preventing the release of inflammatory mediators or inhibiting the actions of released mediators on their target cells. (From AMA Drug Evaluations Annual, 1994, p475) (See all compounds classified as Anti-Allergic Agents.)|Drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine. Included here are the classical antihistaminics that antagonize or prevent the action of histamine mainly in immediate hypersensitivity. They act in the bronchi, capillaries, and some other smooth muscles, and are used to prevent or allay motion sickness, seasonal rhinitis, and allergic dermatitis and to induce somnolence. The effects of blocking central nervous system H1 receptors are not as well understood. (See all compounds classified as Histamine H1 Antagonists.)
Analergine
Computed Properties
Molecular Weight:301.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:301.1345753
Monoisotopic Mass:301.1345753
Topological Polar Surface Area:27.6
Heavy Atom Count:21
Complexity:314
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
It has antiarrhythmic effects, and its mechanism of action is to interfere with the permeability of myocardial cell membranes to sodium and potassium ions, slowing down myocardial conduction; at the same time, it has a mild sympathetic nerve blocking effect, thereby increasing peripheral vascular resistance and reducing cardiac output, with no effect on blood pressure and heart rate, and the action time can last for 4 to 6 hours.
Registered Holders
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Shanghai Yurui BIOTECHNOLOGY (Anyang) Pharmaceutical Co., Ltd.
Active
China
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METROCHEM API PRIVATE LIMITED
Active
European Union
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