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rdf:type
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http://linked.open...gbank/description
| - A carbonic anhydrase inhibitor that is used in the treatment of glaucoma. [PubChem] (en)
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http://linked.open...y/drugbank/dosage
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http://linked.open...generalReferences
| - # Tawil R, McDermott MP, Brown R Jr, Shapiro BC, Ptacek LJ, McManis PG, Dalakas MC, Spector SA, Mendell JR, Hahn AF, Griggs RC: Randomized trials of dichlorphenamide in the periodic paralyses. Working Group on Periodic Paralysis. Ann Neurol. 2000 Jan;47(1):46-53. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/10632100 # Okada S, Izumi W, Murai M, Komatsu H, Ishimitsu S: [Diclofenamide Reference Standard (Control 891) of National Institute of Hygienic Sciences] Eisei Shikenjo Hokoku. 1991;(109):148-50. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/1364383 (en)
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http://linked.open...gy/drugbank/group
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http://linked.open...ugbank/indication
| - For adjunctive treatment of: chronic simple (open-angle) glaucoma, secondary glaucoma, and preoperatively in acute angle-closure glaucoma where delay of surgery is desired in order to lower intraocular pressure (en)
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sameAs
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Title
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adms:identifier
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http://linked.open...mechanismOfAction
| - Carbonic anhydrase inhibitors reduce intraocular pressure by partially suppressing the secretion of aqueous humor (inflow), although the mechanism by which they do this is not fully understood. Evidence suggests that HCO<sup>3-</sup> ions are produced in the ciliary body by hydration of carbon dioxide under the influence of carbonic anhydrase and diffuse into the posterior chamber which contains more Na<sup>+</sup> and HCO<sup>3-</sup> ions than does plasma and consequently is hypertonic. Water is then attracted to the posterior chamber by osmosis, resulting in a drop in pressure. (en)
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http://linked.open.../drugbank/synonym
| - Diclofenamide (en)
- Dichlorphenamide (en)
- Dichlofenamide (en)
- Dichlorophenamide (en)
- 1,3-Disulfamyl-4,5-dichlorobenzene (en)
- 1,3-disulfamoyl-4,5-dichlorobenzene (en)
- 3,4-Dichloro-5-sulfamylbenzenesulfonamide (en)
- 4,5-DICHLOROBENZENE-1,3-disulfonamide (en)
- 4,5-Dichloro-1,3-benzenedisulfonamide (en)
- 4,5-Dichloro-benzene-1,3-disulfonic acid diamide (en)
- 4,5-dichloro-1,3-disulfamoylbenzene (en)
- 4,5-dichloro-m-benzenedisulfonamide (en)
- Diclofenamida (en)
- Diclofenamidum (en)
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http://linked.open...nk/proteinBinding
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http://linked.open...ynthesisReference
| - Schultz,E.M.; U.S.Patent 2,835,702; May 20, 1958; assigned to Merck & Co.,Inc. (en)
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foaf:page
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http://linked.open...ugbank/IUPAC-Name
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http://linked.open...gy/drugbank/InChI
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http://linked.open...Molecular-Formula
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http://linked.open.../Molecular-Weight
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http://linked.open...noisotopic-Weight
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http://linked.open...y/drugbank/SMILES
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http://linked.open.../Water-Solubility
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http://linked.open...ogy/drugbank/logP
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http://linked.open...ogy/drugbank/logS
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http://linked.open...l/drug/hasATCCode
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http://linked.open...nd-Acceptor-Count
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http://linked.open...-Bond-Donor-Count
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http://linked.open...drugbank/InChIKey
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http://linked.open...urface-Area--PSA-
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http://linked.open...nk/Polarizability
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http://linked.open...bank/Refractivity
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http://linked.open...atable-Bond-Count
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http://linked.open.../affectedOrganism
| - Humans and other mammals (en)
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http://linked.open...casRegistryNumber
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http://linked.open...drugbank/category
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http://linked.open...k/Bioavailability
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http://linked.open...bank/Ghose-Filter
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http://linked.open...nk/MDDR-Like-Rule
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http://linked.open...ank/Melting-Point
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http://linked.open...k/Number-of-Rings
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http://linked.open...siological-Charge
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http://linked.open...bank/Rule-of-Five
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http://linked.open...tional-IUPAC-Name
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http://linked.open...strongest-acidic-
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