ジクロフェナミド
- 関
- diclofenamide
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/08/03 21:59:53」(JST)
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Diclofenamide
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Systematic (IUPAC) name |
4,5-dichlorobenzene-1,3-disulfonamide
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Clinical data |
AHFS/Drugs.com |
International Drug Names |
MedlinePlus |
a601233 |
Pharmacokinetic data |
Protein binding |
55% |
Identifiers |
CAS Registry Number |
120-97-8 Y |
ATC code |
S01EC02 |
PubChem |
CID: 3038 |
IUPHAR/BPS |
6807 |
DrugBank |
DB01144 N |
ChemSpider |
2930 Y |
UNII |
VVJ6673MHY Y |
KEGG |
D00518 Y |
ChEBI |
CHEBI:101085 Y |
ChEMBL |
CHEMBL17 Y |
Chemical data |
Formula |
C6H6Cl2N2O4S2 |
Molecular mass |
305.16 g/mol |
SMILES
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Clc1c(cc(cc1Cl)S(=O)(=O)N)S(=O)(=O)N
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InChI
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InChI=1S/C6H6Cl2N2O4S2/c7-4-1-3(15(9,11)12)2-5(6(4)8)16(10,13)14/h1-2H,(H2,9,11,12)(H2,10,13,14) Y
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Key:GJQPMPFPNINLKP-UHFFFAOYSA-N Y
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N (what is this?) (verify) |
Diclofenamide (or dichlorphenamide) is a sulfonamide and a carbonic anhydrase inhibitor of the meta-disulfamoylbenzene class.
Uses
Diclofenamide is used to treat glaucoma[1][2] and therapy-resistant epilepsy.[3]
References
- ^ International Drug Names: Diclofenamide
- ^ Kanski, J. J. (1968). "Carbonic anhydrase inhibitors and osmotic agents in glaucoma. Carbonic anhydrase inhibitors". The British journal of ophthalmology 52 (8): 642–643. doi:10.1136/bjo.52.8.642. PMC 506660. PMID 5724852. edit
- ^ Rucquoy, M.; Sorel, L. (1978). "Diclofenamide in the treatment of therapy-resistant epilepsy". Acta neurologica Belgica 78 (3): 174–182. PMID 352085. edit
Drugs used for glaucoma preparations and miosis (S01E)
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Sympathomimetics |
- Apraclonidine
- Brimonidine (+timolol)
- Clonidine
- Dipivefrine
- Epinephrine
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Parasympathomimetics |
muscarinic |
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muscarinic/nicotinic |
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Acetylcholinesterase inhibitors |
- Demecarium
- Ecothiopate
- Stigmine (Fluostigmine
- Neostigmine
- Physostigmine)
- Paraoxon
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Carbonic anhydrase inhibitors/
(sulfonamides) |
- Acetazolamide
- Brinzolamide (+timolol)
- Diclofenamide
- Dorzolamide (+timolol)
- Methazolamide
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Beta blocking agents |
- Befunolol
- Betaxolol
- Carteolol
- Levobunolol
- Metipranolol
- Timolol
- Mepindolol
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Prostaglandin analogues (F2α) |
- Bimatoprost (+timolol)
- Latanoprost (+timolol)
- Tafluprost
- Travoprost (+timolol)
- Unoprostone
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Other agents |
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Index of the eye
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Description |
- Anatomy
- Physiology
- Phenomena
- appearance
- visual
- optical illusions
- proteins
- Development
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Disease |
- Congenital
- Corneal dystrophy
- Neoplasms and cancer
- Other
- Symptoms and signs
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Treatment |
- Procedures
- Drugs
- infection
- glaucoma and miosis
- mydriatics
- vascular
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UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- Emerging role of calcium-activated potassium channel in the regulation of cell viability following potassium ions challenge in HEK293 cells and pharmacological modulation.
- Tricarico D1, Mele A, Calzolaro S, Cannone G, Camerino GM, Dinardo MM, Latorre R, Conte Camerino D.
- PloS one.PLoS One.2013 Jul 16;8(7):e69551. doi: 10.1371/journal.pone.0069551. Print 2013.
- Emerging evidences suggest that Ca(2+)activated-K(+)-(BK) channel is involved in the regulation of cell viability. The changes of the cell viability observed under hyperkalemia (15 mEq/L) or hypokalemia (0.55 mEq/L) conditions were investigated in HEK293 cells expressing the hslo subunit (hslo-HEK29
- PMID 23874973
- Methazolamide is a new hepatic insulin sensitizer that lowers blood glucose in vivo.
- Konstantopoulos N1, Molero JC, McGee SL, Spolding B, Connor T, de Vries M, Wanyonyi S, Fahey R, Morrison S, Swinton C, Jones S, Cooper A, Garcia-Guerra L, Foletta VC, Krippner G, Andrikopoulos S, Walder KR.
- Diabetes.Diabetes.2012 Aug;61(8):2146-54. doi: 10.2337/db11-0578. Epub 2012 May 14.
- We previously used Gene Expression Signature technology to identify methazolamide (MTZ) and related compounds with insulin sensitizing activity in vitro. The effects of these compounds were investigated in diabetic db/db mice, insulin-resistant diet-induced obese (DIO) mice, and rats with streptozot
- PMID 22586591
- Evaluation of the therapeutic potential of carbonic anhydrase inhibitors in two animal models of dystrophin deficient muscular dystrophy.
- Giacomotto J1, Pertl C, Borrel C, Walter MC, Bulst S, Johnsen B, Baillie DL, Lochmüller H, Thirion C, Ségalat L.
- Human molecular genetics.Hum Mol Genet.2009 Nov 1;18(21):4089-101. doi: 10.1093/hmg/ddp358. Epub 2009 Jul 31.
- Duchenne Muscular Dystrophy is an inherited muscle degeneration disease for which there is still no efficient treatment. However, compounds active on the disease may already exist among approved drugs but are difficult to identify in the absence of cellular models. We used the Caenorhabditis elegans
- PMID 19648295
Japanese Journal
- Crystal Structure of Dichlorphenamide
- Analytical Sciences: X-ray Structure Analysis Online 19, X35-X36, 2003
- NAID 130004442513
- 表面プラズモン共鳴センサーを用いる薬物スクリーニングと初期薬物動態の同時解析(<特集>生体関連機能と分析化学)
- 内科療法のみにて長期間眼圧を制御できた緑内障罹患犬の1例(短報)(臨床病理学)
- The journal of veterinary medical science 63(12), 1323-1325, 2001-12-25
- NAID 110003920797
Related Links
- Physician reviewed dichlorphenamide patient information - includes dichlorphenamide description, dosage and directions. ... Dichlorphenamide dosing information Usual Adult Dose for Primary Periodic Paralysis:-Initial dose: 50 mg ...
- Pregnancy Category C. Dichlorphenamide has been shown to be teratogenic in the rat (skeletal anomalies) when given in doses 100 times the human dose. There are no adequate and well-controlled studies in pregnant ...
Related Pictures
★リンクテーブル★
[★]
- 英
- diuretic, diuretics
- 関
- 尿細管
適応
利尿薬の種類 (GOO.744)
利尿薬の例
-
利尿薬の作用部位
- ホルモンと利尿薬の作用部位についての簡単なまとめは→尿細管
参照
- http://hobab.fc2web.com/sub4-Diuretics.htm
[★]
- 英
- carbonic anhydrase inhibitor, carbonate dehydratase inhibitor
- 関
[★]
ジクロフェナミド
- 関
- dichlorphenamide
[★]
- 英
- dichlorphenamide、diclofenamide