Substance

ID:633

Names and Identifiers
IUPAC Traditional name
epinastine
IUPAC name
2,4-diazatetracyclo[12.4.0.0^{2,6}.0^{7,12}]octadeca-1(14),3,7(12),8,10,15,17-heptaen-3-amine
Synonyms
Epinastinum [Latin]EpinastineEpinastina [Spanish]epinastine
Brand Name
Elestat
Registration numbers
PubChem CID
PubChem SID
CAS Number
Properties
Physical Property
Hydrophobicity(logP)
3.1
Molecule Details
Drug Groups
approved; investigational
Description
Epinastine is used for the prevention of itching associated with allergic conjunctivitis. It has a multi-action effect that inhibits the allergic response in 3 ways: 1. stabilizes mast cells by preventing mast cell degranulation to control the allergic response, 2. prevents histamine binding to both the H1- and H2-receptors to stop itching and provide lasting protection, and 3. prevents the release of proinflammatory chemical mediators from the blood vessel to halt progression of the allergic response.
Indication
For the prevention of itching associated with allergic conjunctivitis.
Pharmacology
Epinastine is an antihistamine and an inhibitor of histamine release from the mast cell for topical administration to the eyes. Epinastine is indicated for the prevention of itching associated with allergic conjunctivitis. Epinastine is a topically active, direct H1-receptor antagonist and an inhibitor of the release of histamine from the mast cell. Epinastine is selective for the histamine H1-receptor and has affinity for the histamine H2 receptor. Epinastine also possesses affinity for the a1-, a2-, and 5-HT2 -receptors. Epinastine does not penetrate the blood/brain barrier and, therefore, is not expected to induce side effects of the central nervous system.
Affected Organisms
Humans and other mammals
Biotransformation
Mainly excreted unchanged, less than 10% metabolized.
Absorption
The absolute bioavailability of epinastine is about 40%.
Half Life
12 hours
Protein Binding
64%
Elimination
Epinastine is mainly excreted unchanged. The renal elimination is mainly via active tubular secretion.
Clearance
* 56 L/hr [patients with allergic conjunctivitis receiving one drop of ELESTAT? ophthalmic solution in each eye twice daily for seven days]
References
• Walther G, Daniel H, Bechtel WD, Brandt K: New tetracyclic guanidine derivatives with H1-antihistaminic properties. Chemistry of epinastine. Arzneimittelforschung. 1990 Apr;40(4):440-6. [Pubmed]
• Schilling JC, Adamus WS, Kuthan H: Antihistaminic activity and side effect profile of epinastine and terfenadine in healthy volunteers. Int J Clin Pharmacol Ther Toxicol. 1990 Dec;28(12):493-7. [Pubmed]
Molecular Spectra
No Data Available
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References
• Schilling JC, Adamus WS, Kuthan H: Antihistaminic activity and side effect profile of epinastine and terfenadine in healthy volunteers. Int J Clin Pharmacol Ther Toxicol. 1990 Dec;28(12):493-7. Pubmed
• Walther G, Daniel H, Bechtel WD, Brandt K: New tetracyclic guanidine derivatives with H1-antihistaminic properties. Chemistry of epinastine. Arzneimittelforschung. 1990 Apr;40(4):440-6. Pubmed