Dekametonijum

Dekametonijum
(IUPAC) ime
	trimetil-(10-trimetilamoniodecil)amonijum
Klinički podaci
Identifikatori
CAS broj	156-74-1
ATC kod	nije dodeljen
PubChem	10921
DrugBank	DB01245
ChemSpider	10459
UNII	C1CG1S3T2W
ChEMBL	CHEMBL1134
Hemijski podaci
Formula	C16H38N2 +
Mol. masa	258,486 g/mol
SMILES	eMolekuli & PubHem
InChI
	InChI=1S/C16H38N2.2BrH/c1-17(2,3)15-13-11-9-7-8-10-12-14-16-18(4,5)6;;/h7-16H2,1-6H3;2*1H/q+2;;/p-2 ; Key: HLXQFVXURMXRPU-UHFFFAOYSA-L
Farmakoinformacioni podaci
Trudnoća	?
Pravni status

Dekametonijum (Syncurine) je depolarizujući mišićni relaksant ili neuromaskularno blokirajući agens.^[5] On se koristi u anesteziji za indukovanje paralize.

Farmakologija

Dekametonijum, koji ima kratko vreme dejstva, je sličan acetilholinu i deluje kao parcijalni agonist nikotinskog acetilholinskog receptora. On uzrokuje depolarizaciju, čime sprečava dalje dejstvo normalnog oslobađanja acetilholina iz presinaptičkih terminala, i stoga sprečava nervne stimuluse u mišićima.

Povezano

Reference

↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
↑ Lee C, Jones T (May 2002). „Molecular conformation-activity relationship of decamethonium congeners”. Br J Anaesth 88 (5): 692–9. DOI:10.1093/bja/88.5.692. PMID 12067008.

Spoljašnje veze

	Portal Medicina
	Portal Hemija

[1] Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[2] Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.

[3] Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[4] Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[pmid12067008-5] Lee C, Jones T (May 2002). „Molecular conformation-activity relationship of decamethonium congeners”. Br J Anaesth 88 (5): 692–9. DOI:10.1093/bja/88.5.692. PMID 12067008.

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