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1 References  














Dimaprit






تۆرکجه
فارسی
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From Wikipedia, the free encyclopedia
 


Dimaprit
Names
Preferred IUPAC name

3-(Dimethylamino)propyl carbamimidothioate

Other names

3-dimethylaminopropyl sulfanylmethanimidamide

Identifiers

CAS Number

3D model (JSmol)

ChEMBL
ChemSpider

IUPHAR/BPS

KEGG

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C6H15N3S/c1-9(2)4-3-5-10-6(7)8/h3-5H2,1-2H3,(H3,7,8) ☒N

    Key: OLHQOJYVQUNWPL-UHFFFAOYSA-N ☒N

  • InChI=1/C6H15N3S/c1-9(2)4-3-5-10-6(7)8/h3-5H2,1-2H3,(H3,7,8)

    Key: OLHQOJYVQUNWPL-UHFFFAOYAQ

  • CN(C)CCCSC(=N)N

Properties

Chemical formula

C6H15N3S
Molar mass 161.2684 g/mol

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

☒N verify (what is checkY☒N ?)

Infobox references

Dimaprit is a histamine analog working as a selective H2 histamine receptor agonist.[1][2][3]

References[edit]

  1. ^ Kartzung, Betram G.; Trevor, Anthony J., eds. (2014). Basic and Clinical Pharmacology (13th ed.). New York: McGraw-Hill Education. p. 364. ISBN 978-0071825054.
  • ^ Kohno, S; Ogawa, K; Nabe, T; Yamamura, H; Ohata, K (May 1993). "Dimaprit, a Histamine H2-agonist, Inhibits Anaphylactic Histamine Release from Mast Cells and the Decreased Release is Restored by Thioperamide (H3-antagonist), but not by Cimetidine (H2-antagonist)". Japanese Journal of Pharmacology. 62 (1): 75–9. doi:10.1254/jjp.62.75. PMID 7688057.
  • ^ Nakamura, T; Ueno, Y; Goda, Y; Nakamura, A; Shinjo, K; Nagahisa, A (March 1997). "Efficacy of a Selective Histamine H2 Receptor Agonist, Dimaprit, in Experimental Models of Endotoxin Shock and Hepatitis in Mice". European Journal of Pharmacology. 322 (1): 83–89. doi:10.1016/S0014-2999(96)00987-9. PMID 9088875.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Dimaprit&oldid=1023318718"

    Categories: 
    Biogenic amines
    Amidines
    Thioethers
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    This page was last edited on 15 May 2021, at 19:05 (UTC).

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