Triampyzine

Triampyzine
Clinical data
Other names(Dimethylamino)trimethylpyrazine; W-3976B; W3976-B; W-3976-B; W3976B; 3,5,6-Trimethylampyzine
Identifiers
IUPAC name
  • N,N,3,5,6-pentamethylpyrazin-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC9H15N3
Molar mass165.240 g·mol−1
3D model (JSmol)
SMILES
  • CC1=C(N=C(C(=N1)C)N(C)C)C
InChI
  • InChI=1S/C9H15N3/c1-6-7(2)11-9(12(4)5)8(3)10-6/h1-5H3
  • Key:RKPVUWPGCFGDJO-UHFFFAOYSA-N

Triampyzine (INNTooltip International Nonproprietary Name), also known as triampyzine sulfate (USANTooltip United States Adopted Name; developmental code name W-3976B) in the case of the sulfate salt, as (dimethylamino)trimethylpyrazine, or as 3,5,6-trimethylampyzine, is a drug described as an anticholinergic and antisecretory agent which was never marketed.[1][2][3][4][5] It was first described in the literature by 1966.[1][6] The drug is the 3,5,6-trimethylated derivative of ampyzine (W-3580B), which is also a drug and is, conversely, described as a "central stimulant".[1][5][2]

References

  1. 1 2 3 Elks, J. (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 436. ISBN 978-1-4757-2085-3. Retrieved 21 October 2024.
  2. 1 2 Milne, G.W.A. (2018). Drugs: Synonyms and Properties. Routledge Revivals. Taylor & Francis. pp. 213, 547. ISBN 978-1-351-78990-5. Retrieved 21 October 2024.
  3. ↑ "TRIAMPYZINE". Inxight Drugs. Retrieved 21 October 2024.
  4. ↑ Negwer, M. (1994). Organic-chemical Drugs and Their Synonyms: (an International Survey). Akademie Verlag. p. 355. ISBN 978-3-05-500156-7. Retrieved 21 October 2024.
  5. 1 2 Lednicer, D. (2009). Strategies for Organic Drug Synthesis and Design. Wiley. p. 366. ISBN 978-0-470-39959-0. Retrieved 21 October 2024.
  6. ↑ Marler, E.E.J. (1967). Pharmacological and Chemical Synonyms: A Collection of Names of Drugs and Other Compounds Drawn from the Medical Literature of the World. Excerpta Medica. p. 322. Retrieved 21 October 2024.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.