Mizolastine
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Mizolastine
structure -
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CAS No:
108612-45-9
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Formula:
C24H25FN6O
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Chemical Name:
Mizolastine
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Synonyms:
4(3H)-Pyrimidinone,2-[[1-[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]-4-piperidinyl]methylamino]-;4(1H)-Pyrimidinone,2-[[1-[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]-4-piperidinyl]methylamino]-;2-[[1-[1-[(4-Fluorophenyl)methyl]-1H-benzimidazol-2-yl]-4-piperidinyl]methylamino]-4(3H)-pyrimidinone;Mizolastine;MKC 431;SL 850324;Zolistan;Mistamine;Mizollen;2-[[1-[1-[(4-Fluorophenyl)methyl]benzimidazol-2-yl]piperidin-4-yl]-methylamino]-1H-pyrimidin-6-one
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CAS No:
Description
White SolidMizolastine was marketed in Germany and Switzerland as Mizollen for the symptomatic relief of seasonal and perennial allergic rhinoconjunctivitis and urticaria. Mizolastine is a new long-acting, orally active antihistaminic agent with a rapid onset of action ; the two most recent H1 antagonists launched were fexofenadine, metabolite of terfenadine (Sepracor, 1996) and Olopatadine (Kyowa Hakko, 1997). Mizolastine can be prepared in 2 steps from 2-chloro 1- (4-fluorobenzyl)benzim
Mizolastine is a member of benzimidazoles.|Mizolastine is under investigation in clinical trial NCT01928316 (A Bioequivalence Study of Domestic (Made in China) and Imported Mizolastine Tablets in Healthy Volunteers).
Mizolastine Basic Attributes
432.49
432.49
1308068-626-2
244O1F90NA
DTXSID5046801
R06AX25|R - Respiratory system
2933990090
Safety Information
UW7481284
|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|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
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.)
Mistalin
Computed Properties
Molecular Weight:432.5
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:432.20738760
Monoisotopic Mass:432.20738760
Topological Polar Surface Area:65.8
Heavy Atom Count:32
Complexity:728
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
2-[[[1-[(4-Fluorophenyl)methyl]-1H-benzoimidazol-2-yl]-4-piperidinyl]methyl-amino]-4(3H)-pyrimidinone
Registered Holders
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Opella Healthcare Shanghai Ltd
Active
China
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Shenyang Sanjiu Pharmaceutical Co., Ltd.
Active
China
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Beijing Jialin Pharmaceutical Co., Ltd.
Active
China
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