Mersalyl acid: Difference between revisions

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Mersalyl acid
Names
	Other names Mersalyl acid, salyrganic acid
Identifiers
CAS Number	486-67-9 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL1201330 ;
ChemSpider	11337655 ;
ECHA InfoCard	Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value).
PubChem CID	443130;
UNII	5X1IO031V8;
	InChI InChI=1S/C13H16NO5.Hg.H2O/c1-9(18-2)7-14-13(17)10-5-3-4-6-11(10)19-8-12(15)16;;/h3-6,9H,1,7-8H2,2H3,(H,14,17)(H,15,16);;1H2/q;+1;/p-1 Key: HQRSUIDICNOLPX-UHFFFAOYSA-M ; InChI=1/C13H16NO5.Hg.H2O/c1-9(18-2)7-14-13(17)10-5-3-4-6-11(10)19-8-12(15)16;;/h3-6,9H,1,7-8H2,2H3,(H,14,17)(H,15,16);;1H2/q;+1;/p-1/rC13H17HgNO6/c1-20-9(6-14-19)7-15-13(18)10-4-2-3-5-11(10)21-8-12(16)17/h2-5,9,19H,6-8H2,1H3,(H,15,18)(H,16,17) Key: HQRSUIDICNOLPX-SCJHNVIKAK;
	SMILES O[Hg]CC(OC)CNC(=O)c1ccccc1OCC(O)=O;
Properties
Chemical formula	C13H18HgNO6
Molar mass	484.87512
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

VisualWikitext

Latest revision as of 01:28, 25 July 2014

Template:Chembox E number

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Mersalyl (Mersal) is an organomercury compound. It is only rarely used as a drug, having been superseded by diuretic medications that do not contain mercury and are therefore less toxic. It features a Hg(II) centre. Mersalyl was originally adapted from calomel (HgCl), a diuretic discovered by Paracelsus.

References

@@ Line 1: / Line 1: @@
-[[Image:Mersalyl_svg.png|thumb|220px|[[Chemical structure]] of mersalyl]]
+{{Chembox
+| Verifiedfields = changed
+| verifiedrevid = 400297609
+|ImageFile=MersalylLinearHg.png
+|ImageSize=
+|IUPACName=
+|OtherNames=Mersalyl acid, salyrganic acid
+|Section1={{Chembox Identifiers
+| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
+| ChemSpiderID = 11337655
+| ChEMBL_Ref = {{ebicite|changed|EBI}}
+| ChEMBL = 1201330
+| InChI = 1/C13H16NO5.Hg.H2O/c1-9(18-2)7-14-13(17)10-5-3-4-6-11(10)19-8-12(15)16;;/h3-6,9H,1,7-8H2,2H3,(H,14,17)(H,15,16);;1H2/q;+1;/p-1/rC13H17HgNO6/c1-20-9(6-14-19)7-15-13(18)10-4-2-3-5-11(10)21-8-12(16)17/h2-5,9,19H,6-8H2,1H3,(H,15,18)(H,16,17)
+| InChIKey = HQRSUIDICNOLPX-SCJHNVIKAK
+| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
+| StdInChI = 1S/C13H16NO5.Hg.H2O/c1-9(18-2)7-14-13(17)10-5-3-4-6-11(10)19-8-12(15)16;;/h3-6,9H,1,7-8H2,2H3,(H,14,17)(H,15,16);;1H2/q;+1;/p-1
+| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
+| StdInChIKey = HQRSUIDICNOLPX-UHFFFAOYSA-M
+| CASNo_Ref = {{cascite|correct|??}}
+| CASNo=486-67-9
+| UNII = 5X1IO031V8
+| PubChem=443130
+| SMILES = O[Hg]CC(OC)CNC(=O)c1ccccc1OCC(O)=O
+| ATCCode_prefix = C03
+| ATCCode_suffix = BC01
+}}
+|Section2={{Chembox Properties
+|  Formula=C<sub>13</sub>H<sub>18</sub>HgNO<sub>6</sub>
+|  MolarMass=484.87512
+|  Appearance=
+|  Density=
+|  MeltingPt=
+|  BoilingPt=
+|  Solubility=
+  }}
+|Section3={{Chembox Hazards
+|  MainHazards=
+|  FlashPt=
+|  Autoignition=
+  }}
+}}
+__NOTOC__
+{{SI}}
 {{CMG}}
-{{Editor Join}}
+==Overview==
+'''Mersalyl''' (Mersal) is an organomercury compound.  It is only rarely used as a drug, having been superseded by [[diuretic|diuretic medications]] that do not contain [[mercury (element)|mercury]] and are therefore less toxic.  It features a Hg(II) centre. Mersalyl was originally adapted from calomel (HgCl), a diuretic discovered by Paracelsus.
-'''Mersalyl acid''' (Mersal) is a [[mercurial diuretic]].  It is only rarely used, having been superseded by [[diuretic|diuretic medications]] that do not contain [[mercury (element)|mercury]] and are therefore less toxic.
+==References==
+{{reflist|2}}
-{{Antihypertensives and diuretics}}
 [[Category:Diuretics]]
-[[Category:Mercury compounds]]
+[[Category:Cardiovascular Drugs]]
-[[Category:Drugs]]
+[[Category:Drug]]
-{{WikiDoc Help Menu}}
-{{WikiDoc Sources}}

Mersalyl acid: Difference between revisions

Latest revision as of 01:28, 25 July 2014

Overview

References

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