Levocabastine hydrochloride
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Levocabastine hydrochloride
structure -
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CAS No:
79547-78-7
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Formula:
C26H29FN2O2.ClH
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Chemical Name:
Levocabastine hydrochloride
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Synonyms:
4-Piperidinecarboxylic acid,1-[cis-4-cyano-4-(4-fluorophenyl)cyclohexyl]-3-methyl-4-phenyl-,hydrochloride (1:1),(3S,4R)-;4-Piperidinecarboxylic acid,1-[4-cyano-4-(4-fluorophenyl)cyclohexyl]-3-methyl-4-phenyl-,monohydrochloride,[3S-[1(cis),3α,4β]]-;4-Piperidinecarboxylic acid,1-[cis-4-cyano-4-(4-fluorophenyl)cyclohexyl]-3-methyl-4-phenyl-,monohydrochloride,(3S,4R)-;Levocabastine hydrochloride;Livostin
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CAS No:
Description
White or almost white powder.
Livostin (TN) is a member of piperidines.|Levocabastine Hydrochloride is the hydrochloride salt form of levocabastine, a synthetic piperidine derivative with antihistaminic properties. Levocabastine is a second generation histamine-1 receptor antagonist. When applied locally to the eye as a topical solution, this agent reduces itching, rhinorrhea, and symptoms of allergic rhinitis or conjunctivitis.
Levocabastine hydrochloride Basic Attributes
456.98
456.19800
124XMA6YEI
DTXSID9045508
C47582
2933399090
Characteristics
64.33000
5.63398
white solid
611ºC at 760 mmHg
323.3ºC
DMSO: ~10 mg/mL, soluble
2-8°C
Safety Information
NONH for all modes of transport
3
36/37/38
26-36
Xi
P305 + P351 + P338
H315-H319-H335
|Warning|H315 (97.5%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, 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
A class of non-sedating drugs that bind to but do not activate histamine receptors (DRUG INVERSE AGONISM), thereby blocking the actions of histamine or histamine agonists. These antihistamines represent a heterogenous group of compounds with differing chemical structures, adverse effects, distribution, and metabolism. Compared to the early (first generation) antihistamines, these non-sedating antihistamines have greater receptor specificity, lower penetration of BLOOD-BRAIN BARRIER, and are less likely to cause drowsiness or psychomotor impairment. (See all compounds classified as Histamine H1 Antagonists, Non-Sedating.)
1-(4-cyano-4-(4-fluorophenyl)cyclohexyl)-3-methyl-4-phenyl-4-piperidinecarboxylic acid
Levocabastine hydrochloride Use and Manufacturing
A histamine H1 receptor antagonist
Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients
Computed Properties
Molecular Weight:457.0
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:456.1979841
Monoisotopic Mass:456.1979841
Topological Polar Surface Area:64.3
Heavy Atom Count:32
Complexity:681
Defined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Levocabastine hydrochloride is a potent, long-acting, highly selective histamine H1 receptor antagonist. When applied topically to the nose, it takes effect almost immediately, eliminating the typical symptoms of allergic rhinitis (sneezing, itchy nose, runny nose), and the effect can last for several hours.
Registered Holders
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Guangzhou Tosun Pharmaceutical Ltd
Active
China
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JANSSEN PHARMACEUTICA NV
Active
European Union
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KATSURA CHEMICAL CO., LTD.
Active
European Union
Recommended Suppliers of Levocabastine hydrochloride
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