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MTEP

Izvor: Wikipedija
MTEP
(IUPAC) ime
3-[(2-metil-1,3-tiazol-4-il)etinil]piridin
Klinički podaci
Identifikatori
CAS broj 329205-68-7
ATC kod nije dodeljen
PubChem[1][2] 9794218
Hemijski podaci
Formula C11H8N2S
Mol. masa 200,260 g/mol
SMILES eMolekuli&PubHem
Farmakoinformacioni podaci
Trudnoća ?
Pravni status

3-[(2-Metil-4-tiazolil)etinil]piridin(MTEP) je lek koji se koristi u naučnim istraživanjima. Razvila ga je kompanijaMerck & Co..On je selektivanalosteranantagonistmetabotropnog glutamatnog receptoramGluR5.On je identifikovan putem studijaodnosa strukture i aktivnostistarijeg mGluR5 antagonistaMPEP.[3]MTEP je naknadno korišten kaovodeće jedinjenjeza novije i potentnije lekiva.[4][5]

Reference

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  1. Li Q, Cheng T, Wang Y, Bryant SH (2010).„PubChem as a public resource for drug discovery.”.Drug Discov Today15(23-24): 1052-7.DOI:10.1016/j.drudis.2010.10.003.PMID20970519.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 Chemistry4:217-241.DOI:10.1016/S1574-1400(08)00012-1.
  3. Cosford ND, Tehrani L, Roppe J,et al.(January 2003). „3-[(2-Methyl-1,3-thiazol-4-yl)ethynyl]-pyridine: a potent and highly selective metabotropic glutamate subtype 5 receptor antagonist with anxiolytic activity”.J. Med. Chem.46(2): 204–6.DOI:10.1021/jm025570j.PMID12519057.
  4. Iso Y, Grajkowska E, Wroblewski JT,et al.(February 2006). „Synthesis and structure-activity relationships of 3-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyridine analogues as potent, noncompetitive metabotropic glutamate receptor subtype 5 antagonists; search for cocaine medications”.J. Med. Chem.49(3): 1080–100.DOI:10.1021/jm050570f.PMID16451073.
  5. Kulkarni SS, Newman AH (June 2007).„Discovery of heterobicyclic templates for novel metabotropic glutamate receptor subtype 5 antagonists”.Bioorg. Med. Chem. Lett.17(11): 2987–91.DOI:10.1016/j.bmcl.2007.03.066.PMC1973162.PMID17446071.

Spoljašnje veze

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