About: Bepotastine

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An Entity of Type : http://linked.opendata.cz/ontology/drugbank/Drug, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	http://linked.opendata.cz/ontology/drugbank/Drug
http://linked.open...gbank/description	Bepotastine is a non-sedating, selective antagonist of the histamine 1 (H1) receptor. Bepotastine was approved in Japan for use in the treatment of allergic rhinitis and uriticaria/puritus in July 2000 and January 2002, respectively, and is marketed by Tanabe Seiyaku Co., Ltd. under the brand name Talion. It is available in oral and opthalmic dosage forms in Japan. The opthalmic solution is FDA approved since Sept 8, 2009 and is under the brand name Bepreve. (en)
http://linked.open...y/drugbank/dosage	http://linked.opendata.cz/resource/drugbank/dosage/271B5D75-363D-11E5-9242-09173F13E4C5
http://linked.open...generalReferences	# Ohashi R, Kamikozawa Y, Sugiura M, Fukuda H, Yabuuchi H, Tamai I: Effect of P-glycoprotein on intestinal absorption and brain penetration of antiallergic agent bepotastine besilate. Drug Metab Dispos. 2006 May;34(5):793-9. Epub 2006 Feb 2. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/16455807 # Andoh T, Kuraishi Y: Suppression by bepotastine besilate of substance P-induced itch-associated responses through the inhibition of the leukotriene B4 action in mice. Eur J Pharmacol. 2006 Oct 10;547(1-3):59-64. Epub 2006 Jul 25. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/16914135 # Simons FE, Simons KJ: Histamine and H1-antihistamines: celebrating a century of progress. J Allergy Clin Immunol. 2011 Dec;128(6):1139-1150.e4. doi: 10.1016/j.jaci.2011.09.005. Epub 2011 Oct 27. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/22035879 # Wingard JB, Mah FS: Critical appraisal of bepotastine in the treatment of ocular itching associated with allergic conjunctivitis. Clin Ophthalmol. 2011;5:201-7. doi: 10.2147/OPTH.S8665. Epub 2011 Feb 15. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/21386912 (en)
http://linked.open...gy/drugbank/group	approved (en)
http://linked.open...drugbank/halfLife	Elimination half life = 2.5 hours (en)
http://linked.open...ugbank/indication	For the symptomatic treatment of itchy eyes (caused by IgE-induced mast cell degranulation) due to allergic conjunctivitis. (en)
sameAs	Bepotastine Bepotastine
Title	Bepotastine (en)
adms:identifier	http://linked.opendata.cz/resource/drugbank/drug/DB04890/identifier/chemspider/2260 http://linked.opendata.cz/resource/drugbank/drug/DB04890/identifier/drugbank/DB04890 http://linked.opendata.cz/resource/drugbank/drug/DB04890/identifier/kegg-drug/D01654 http://linked.opendata.cz/resource/drugbank/drug/DB04890/identifier/pubchem-compound/2350 http://linked.opendata.cz/resource/drugbank/drug/DB04890/identifier/pubchem-substance/46504940 http://linked.opendata.cz/resource/drugbank/drug/DB04890/identifier/chebi/71204 http://linked.opendata.cz/resource/drugbank/drug/DB04890/identifier/national-drug-code-directory/54868-6299-0 http://linked.opendata.cz/resource/drugbank/drug/DB04890/identifier/pharmgkb/PA164781356 http://linked.opendata.cz/resource/drugbank/drug/DB04890/identifier/wikipedia/Bepotastine
http://linked.open...mechanismOfAction	Because of a type 1 hypersensitivity reaction cascade that is triggered by antigen exposure, allergic conjunctivitis occurs. Allergen exposure is followed by conjunctival mast cell degranulation and histamine released as a result of the formation of complementary IgE cross-links on the conjunctiva. Due to the release of histamine, symptoms such as itching can be observed. Bepotastine works to relieve itchy eyes by three primary mechanisms of action. It is a non-sedating, selective antagonist of the histamine 1 (H1) receptor, a mast cell stabilizer, and it suppresses the migration of eosinophils into inflamed tissues to prevent tissue damage and worsening of allergic inflammation of the conjunctiva. (en)
http://linked.open...drugbank/packager	Amerisource Health Services Corp.
http://linked.open...y/drugbank/patent	http://linked.opendata.cz/resource/drugbank/patent/6780877
http://linked.open...outeOfElimination	When a oral dose of 2.5 - 40 mg bepotastine is given, 75%-90% of the dose was excreted unchanged in the urine by 24 hours. (en)
http://linked.open.../drugbank/synonym	TAU-284DS (en)
http://linked.open.../drug/hasAHFSCode	http://linked.opendata.cz/resource/AHFS/52-02
http://linked.open...nk/proteinBinding	55.4% mean plasma protein binding with 10 mg oral dose. Extent of protein binding is independent of plasma drug concentration. (en)
http://linked.open...ogy/drugbank/salt	(en)
http://linked.open...ynthesisReference	Tae Hee Ha, Chang Hee Park, Won Jeoung Kim, Soohwa Cho, Han Kyong Kim, Kwee Hyun Suh, "PROCESS FOR PREPARING BEPOTASTINE AND INTERMEDIATES USED THEREIN." U.S. Patent US20100168433, issued July 01, 2010. (en)
http://linked.open...y/mesh/hasConcept	http://linked.opendata.cz/resource/mesh/concept/M0281815
foaf:page	http://www.drugs.com/cdi/bepotastine-eye-drops.html http://www.pdrhealth.com/drugs/bepreve http://www.rxlist.com/bepreve-drug.htm
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http://linked.open...ugbank/absorption	Tmax, after single dose, opthalmic = 1.2 hours; Cmax, 1.5%, opthalmic dose = 7.3 ±1.9 ng/mL; After 24 hours post-installation, levels of bepotastine are below quantifiable limit of 2 ng/mL. Minimal systemic absorption with opthalmic dosage form. (en)
http://linked.open.../affectedOrganism	Humans and other mammals (en)
http://linked.open...casRegistryNumber	125602-71-3 (en)
http://linked.open...drugbank/category	(en)
http://linked.open...gbank/containedIn	Bepreve 1.5% eye drops
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