Betahistine mesylate
-
Betahistine mesylate
structure -
-
CAS No:
54856-23-4
-
Formula:
C8H12N2.2CH4O3S
-
Chemical Name:
Betahistine mesylate
-
Synonyms:
2-Pyridineethanamine,N-methyl-,methanesulfonate (1:2);2-Pyridineethanamine,N-methyl-,dimethanesulfonate;Betahistine mesylate;Merislon
-
Categories:
Active Pharmaceutical Ingredients > Circulatory System Drugs
-
CAS No:
Description
White or almost white, crystalline powder, very hygroscopic.
Betahistine mesilate is an aralkylamine.|A histamine analog and H1 receptor agonist that serves as a vasodilator. It is used in MENIERE DISEASE and in vascular headaches but may exacerbate bronchial asthma and peptic ulcers.
Betahistine mesylate Basic Attributes
328.41
328.076263
259-377-7
X1L0E3R43Y
DTXSID1045588
2933399090
Characteristics
150.42000
2.40400
112°C
210.9ºC at 760 mmHg
96.7ºC
almost transparency
Oral-rat LD50: 3030 mg/kg; Oral-Mouse LD50: 500 mg/kg
Flammable; burning produces toxic nitrogen oxides and sulfur oxide fumes
Safety Information
UT2970200
Ventilated, low temperature and dry
P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362
H315
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
Drug Information
Drugs that bind to and activate histamine receptors. Although they have been suggested for a variety of clinical applications histamine agonists have so far been more widely used in research than therapeutically. (See all compounds classified as Histamine Agonists.)|Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)
Aequamen
Computed Properties
Molecular Weight:328.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:328.07627871
Monoisotopic Mass:328.07627871
Topological Polar Surface Area:150
Heavy Atom Count:20
Complexity:176
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes
Drug Function and Efficacy
1. Improvement of inner ear circulation disorders: In the marmot model, blood flow increased to 148% 30 minutes after intraperitoneal administration. 2. Increased cochlear blood flow in marmots with endolymphatic edema: Cochlear blood flow increased from 5.5ml/(100g·min) to 8.1ml/(100g·min), due to the relaxation of the smooth muscle of the radial arteries of the cochlea. 3. Improvement of brain blood flow: In the rhesus monkey experiment, after intravenous injection, the blood flow of the cerebral and cerebellar tissues increased from 70.4ml/(100g·min) to 81.1ml/(100g·min) and from 73.2ml/(100g·min) to 84.0ml/(100g·min), respectively.
Registered Holders
-
China CHINO PHARMA Ltd
Active
China
-
Xiamen Encheng Tragacanth Limited Company
Active
China
-
Lanxiha Sanlian Pharmaceutical Co., Ltd.
Active
China
Recommended Suppliers of Betahistine mesylate
-
CN
4 YRS
Business licensed Certified factoryManufactory Supplier of Betahistine Mesylate,Azilsartan Medoxomil Potassium,Pimavanserin Tartrate,Iguratimod -
CN
3 YRS
Business licensedTrader Supplier of api,Intermediates,Organic Chemistry,Inorganic Chemistry,Daily Chemicals,Cosmetic Raw Materals,CATALYST AND AUXILIARY,FLAVORS AND FRAGRANCES,Chemical Pesticides,ADDITIVE
Learn More Other Chemicals
-
Benzyl oxopropyl mesylate
98518-10-6
-
Isoetharine mesylate
7279-75-6
-
Danofloxacin-d3 Mesylate
1217860-94-0
-
Des[3-[[(1-CarboxyMethyl)cyclopropyl]Methyl]thio]-2-propenyl Montelukast Mesylate Formula
1187586-82-8
-
Bitolterol mesylate Formula
30392-41-7
-
Casopitant mesylate Formula
414910-30-8
-
Safinamide mesylate Structure
202825-46-5
-
5-Chloro Bifeprunox Mesylate Structure
1217042-05-1
-
What is Pralidoxime mesylate
154-97-2
-
What is GATIFLOXACIN MESYLATE
316819-28-0