Wikipedia:WikiProject Chemicals/Chembox validation/VerifiedDataSandbox and Acetohexamide: Difference between pages

(Difference between pages)
Page 1
Page 2
Content deleted Content added
Saving copy of the {{drugbox}} taken from revid 457487337 of page Acetohexamide for the Chem/Drugbox validation project (updated: 'DrugBank').
 
→‎Risks: removed instructional language per MOS:INSTRUCT
Tags: Mobile edit Mobile web edit Advanced mobile edit
 
Line 1: Line 1:
{{Short description|Chemical compound}}
{{ambox | text = This page contains a copy of the infobox ({{tl|drugbox}}) taken from revid [{{fullurl:Acetohexamide|oldid=457487337}} 457487337] of page [[Acetohexamide]] with values updated to verified values.}}
{{distinguish|acetazolamide}}
{{Drugbox
{{Drugbox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 457457565
| verifiedrevid = 477239096
| IUPAC_name = 4-acetyl-''N''-(cyclohexylcarbamoyl)benzenesulfonamide
| IUPAC_name = 1-[(4-acetylbenzene)sulfonyl]-3-cyclohexylurea
| image = Acetohexamide.svg


4-acetyl-''N''-(cyclohexylcarbamoyl)benzenesulfonamide
| image = Acetohexamide.svg
| image2 = Acetohexamide_ball-and-stick.png
<!--Clinical data-->
<!--Clinical data-->
| tradename = Dymelor
| tradename = Dymelor
Line 13: Line 16:
| legal_status =
| legal_status =
| routes_of_administration =
| routes_of_administration =

<!--Pharmacokinetic data-->
<!--Pharmacokinetic data-->
| bioavailability =
| bioavailability =
Line 19: Line 21:
| metabolism =
| metabolism =
| elimination_half-life =
| elimination_half-life =

<!--Identifiers-->
<!--Identifiers-->
| IUPHAR_ligand = 6793
| CASNo_Ref = {{cascite|correct|CAS}}
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 968-81-0
| CAS_number = 968-81-0
Line 28: Line 29:
| ATC_supplemental =
| ATC_supplemental =
| PubChem = 1989
| PubChem = 1989
| DrugBank_Ref = {{drugbankcite|changed|drugbank}}
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = DB00414
| DrugBank = DB00414
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
Line 40: Line 41:
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 1589
| ChEMBL = 1589

<!--Chemical data-->
<!--Chemical data-->
| C=15 | H=20 | N=2 | O=4 | S=1
| C=15 | H=20
| N=2 | O=4
| S=1
| molecular_weight = 324.395 g/mol
| smiles = O=C(NC1CCCCC1)NS(=O)(=O)c2ccc(C(=O)C)cc2
| smiles = O=C(NC1CCCCC1)NS(=O)(=O)c2ccc(C(=O)C)cc2
| InChI = 1/C15H20N2O4S/c1-11(18)12-7-9-14(10-8-12)22(20,21)17-15(19)16-13-5-3-2-4-6-13/h7-10,13H,2-6H2,1H3,(H2,16,17,19)
| InChIKey = VGZSUPCWNCWDAN-UHFFFAOYAN
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C15H20N2O4S/c1-11(18)12-7-9-14(10-8-12)22(20,21)17-15(19)16-13-5-3-2-4-6-13/h7-10,13H,2-6H2,1H3,(H2,16,17,19)
| StdInChI = 1S/C15H20N2O4S/c1-11(18)12-7-9-14(10-8-12)22(20,21)17-15(19)16-13-5-3-2-4-6-13/h7-10,13H,2-6H2,1H3,(H2,16,17,19)
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = VGZSUPCWNCWDAN-UHFFFAOYSA-N
| StdInChIKey = VGZSUPCWNCWDAN-UHFFFAOYSA-N
| melting_point = 188
| melting_high = 190
}}
}}

'''Acetohexamide''' (trade name '''Dymelor''') is a first-generation [[sulfonylurea]] [[medication]] used to treat [[diabetes mellitus type 2]], particularly in people whose diabetes cannot be controlled by diet alone.<ref name="pmid14216839">{{cite journal | vauthors = Montgomery DA | title = Current Therapeutics. CCII. Acetohexamide | journal = The Practitioner | volume = 193 | issue = | pages = 555–60 | date = October 1964 | pmid = 14216839 | doi = | url = }}</ref>

==Mechanism of action==

Acetohexamide bind to an [[ATP-sensitive potassium channel|ATP-sensitive K<sup>+</sup>]] (K<sub>ATP</sub>) channel on the cell membrane of [[pancreatic beta cell]]s. This inhibits the out flux of [[potassium in biology|potassium]], which causes the [[membrane potential]] to become more positive. This depolarization in turn opens [[voltage-gated calcium channel]]s. The rise in intracellular [[calcium in biology|calcium]] leads to increased fusion of [[Granule_(cell_biology)#Insulin_granules_in_beta_cells|insulin granulae]] with the cell membrane, and therefore increased secretion of insulin.<ref>{{cite web | title = Acetohexamide | url = https://go.drugbank.com/drugs/DB00414 | work = DrugBank }}</ref>

==Risks==
Oral hypoglycemic drugs, including acetohexamide, have been associated with increased [[cardiovascular]] mortality. Qualified healthcare professionals should consulted for possible risks, benefits, and alternatives of using this drug for treatment of type 2 diabetes.<ref>{{cite web | title = Acetohexamide | url = https://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a682478.html | work = Medline Plus | archive-url = https://web.archive.org/web/20050911024428/http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a682478.html | archive-date = 11 September 2005 }}</ref>

==References==
{{Reflist}}


{{Oral hypoglycemics}}
{{Ion channel modulators}}

[[Category:Potassium channel blockers]]
[[Category:1-(Benzenesulfonyl)-3-cyclohexylureas]]
[[Category:Aromatic ketones]]

{{Gastrointestinal-drug-stub}}