{{chembox | Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 360226931 | ImageFile = Dimaprit.svg | ImageSize = 222 | PIN = 3-(Dimethylamino)propyl carbamimidothioate | OtherNames = 3-dimethylaminopropyl sulfanylmethanimidamide

| Section1 = {{Chembox Identifiers | CASNo_Ref = {{cascite|correct|??}} | CASNo = 65119-89-3 | PubChem = 3077 | ChEMBL_Ref = {{ebicite|changed|EBI}} | ChEMBL = 12344 | IUPHAR_ligand = 1248 | UNII_Ref = {{fdacite|changed|FDA}} | UNII = ZZQ699148P | KEGG_Ref = {{keggcite|changed|kegg}} | KEGG = C17930 | SMILES = CN(C)CCCSC(=N)N | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID = 2968 | InChI = 1/C6H15N3S/c1-9(2)4-3-5-10-6(7)8/h3-5H2,1-2H3,(H3,7,8) | InChIKey = OLHQOJYVQUNWPL-UHFFFAOYAQ | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 1S/C6H15N3S/c1-9(2)4-3-5-10-6(7)8/h3-5H2,1-2H3,(H3,7,8) | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = OLHQOJYVQUNWPL-UHFFFAOYSA-N }}

| Section2 = {{Chembox Properties | Formula = C<sub>6</sub>H<sub>15</sub>N<sub>3</sub>S | MolarMass = 161.2684 g/mol | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }}

| Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}

'''Dimaprit''' is a histamine analog working as a selective H<sub>2</sub> histamine receptor agonist.<ref>{{cite book|editor1-last=Kartzung|editor1-first=Betram G.|editor2-last=Trevor|editor2-first=Anthony J.|title=Basic and Clinical Pharmacology|date=2014|publisher=McGraw-Hill Education|location=New York|isbn=978-0071825054|page=364|edition=13th}}</ref><ref>{{cite journal|last1=Kohno|first1=S|last2=Ogawa|first2=K|last3=Nabe|first3=T|last4=Yamamura|first4=H|last5=Ohata|first5=K|title=Dimaprit, a Histamine H<sub>2</sub>-agonist, Inhibits Anaphylactic Histamine Release from Mast Cells and the Decreased Release is Restored by Thioperamide (H<sub>3</sub>-antagonist), but not by Cimetidine (H<sub>2</sub>-antagonist)|journal=Japanese Journal of Pharmacology|date=May 1993|volume=62|issue=1|pages=75–9|pmid=7688057|doi=10.1254/jjp.62.75|doi-access=free}}<!--|access-date=7 January 2016--></ref><ref>{{cite journal|last1=Nakamura|first1=T|last2=Ueno|first2=Y|last3=Goda|first3=Y|last4=Nakamura|first4=A|last5=Shinjo|first5=K|last6=Nagahisa|first6=A|title=Efficacy of a Selective Histamine H<sub>2</sub> Receptor Agonist, Dimaprit, in Experimental Models of Endotoxin Shock and Hepatitis in Mice|journal=European Journal of Pharmacology|date=March 1997|volume=322|issue=1|pages=83–89|doi=10.1016/S0014-2999(96)00987-9|pmid=9088875}}<!--|access-date=7 January 2016--></ref>

==References== {{reflist}}

{{Histaminergics}}

Category:Biogenic amines Category:Amidines Category:Thioethers Category:Imidothiocarbamates Category:Dimethylamino compounds Category:Propylthio compounds