Fenspiride hydrochloride
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Fenspiride hydrochloride
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CAS No:
5053-08-7
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Formula:
C15H20N2O2.ClH
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Chemical Name:
Fenspiride hydrochloride
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Synonyms:
1-Oxa-3,8-diazaspiro[4.5]decan-2-one,8-(2-phenylethyl)-,hydrochloride (1:1);1-Oxa-3,8-diazaspiro[4.5]decan-2-one,8-phenethyl-,monohydrochloride;1-Oxa-3,8-diazaspiro[4.5]decan-2-one,8-(2-phenylethyl)-,monohydrochloride;Fenspiride hydrochloride;JP 428;8-Phenethyl-1-oxa-3,8-diazaspiro[4.5]decan-2-one hydrochloride;Decaspiride;Fluiden;Viarespan;NAT 333;Decaspir;Tegencia;NDR 5998A;Pneumorel;Erespal
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CAS No:
Description
Fenspiride Hcl is an α adrenergic and H1 histamine receptor antagonist.IC50 value:Target: Adrenergic receptor; H1 receptorFenspiride hydrochloride is a bronchodilator with anti-inflammatory properties. Fenspiride hydrochloride inhibits mucus secretion and reduces the release of tachykinins at a prejunctional level. Fenspiride hydrochloride also may be an antagonist at α adrenergic and H1 histamine receptors.
Fenspiride hydrochloride Basic Attributes
296.79
296.12900
225-752-9
832NBX878V
757825
DTXSID3045770
Characteristics
41.6
2.87220
white powder
1.19g/cm3
235-238°C (dec.)
474.3ºC at 760mmHg
240.6ºC
>44.5 [ug/mL]
Refrigerator
LD50 i.v. in mice: 106 mg/kg; orally in rats: 437 mg/kg (LeDouarec)
148.9 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]
Safety Information
NONH for all modes of transport
3
20/21/22
36
RO0375000
Xn
P280
H302-H312-H332
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, and P501|Aggregated GHS information provided by 42 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Agents that cause an increase in the expansion of a bronchus or bronchial tubes. (See all compounds classified as Bronchodilator Agents.)
3612 S
Fenspiride hydrochloride Use and Manufacturing
Bronchodilator with anti-inflammatory properties. Inhibits mucus secretion and reduces the release of tachykinins at a prejunctional level by its anti-muscarinic action. It also may be an antagonist at α adrenergic and H1 histamine receptors.
Computed Properties
Molecular Weight:296.79
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:296.1291556
Monoisotopic Mass:296.1291556
Topological Polar Surface Area:41.6
Heavy Atom Count:20
Complexity:318
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
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