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Topiramat

С Википедије, слободне енциклопедије
Topiramat
Klinički podaci
Prodajno imeTopamax, Topamax Sprinkle
Drugs.comMonografija
Način primeneOralno
Farmakokinetičkipodaci
Poluvreme eliminacije19 - 23 h
Identifikatori
CAS broj97240-79-4ДаY
ATC kodN03AX11(WHO)
PubChemCID5284627
DrugBankDB00273ДаY
ChemSpider4447672ДаY
KEGGC07502ДаY
ChEMBLCHEMBL220492ДаY
Hemijski podaci
FormulaC12H21NO8S
Molarna masa339,362
  • [H][C@@]12CO[C@@]3(COS(N)(=O)=O)OC(C)(C)O[C@@]3([H])[C@]1([H])OC(C)(C)O2
  • InChI=1S/C12H21NO8S/c1-10(2)18-7-5-16-12(6-17-22(13,14)15)9(8(7)19-10)20-11(3,4)21-12/h7-9H,5-6H2,1-4H3,(H2,13,14,15)/t7-,8-,9+,12+/m1/s1ДаY
  • Key:KJADKKWYZYXHBB-XBWDGYHZSA-NДаY

Topiramatjeorgansko jedinjenje,koje sadrži 12atomaugljenikai imamolekulsku masuod 339,362Da.[1][2][3]

Osobina Vrednost
Broj akceptora vodonika 8
Broj donora vodonika 1
Broj rotacionih veza 3
Particioni koeficijent[4](ALogP) -1,9
Rastvorljivost[5](logS,log(mol/L)) -0,9
Polarna površina[6](PSA,Å2) 123,9
  1. ^Blum D, Meador K, Biton V, Fakhoury T, Shneker B, Chung S, Mills K, Hammer A, Isojarvi J: Cognitive effects of lamotrigine compared with topiramate in patients with epilepsy. Neurology. 2006 Aug 8;67(3):400-6.PMID16894098
  2. ^Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS (2011).„DrugBank 3.0: a comprehensive resource for omics research on drugs”.Nucleic Acids Res.39(Database issue): D1035—41.PMC3013709Слободан приступ.PMID21059682.doi:10.1093/nar/gkq1126.уреди
  3. ^David S. Wishart; Craig Knox; An Chi Guo; Dean Cheng; Savita Shrivastava; Dan Tzur; Bijaya Gautam; Murtaza Hassanali (2008).„DrugBank: a knowledgebase for drugs, drug actions and drug targets”.Nucleic acids research.36(Database issue): D901—6.PMC2238889Слободан приступ.PMID18048412.doi:10.1093/nar/gkm958.уреди
  4. ^Ghose, A.K.; Viswanadhan V.N. & Wendoloski, J.J. (1998).„Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragment Methods: An Analysis of AlogP and CLogP Methods”.J. Phys. Chem. A.102:3762—3772.doi:10.1021/jp980230o.
  5. ^Tetko IV, Tanchuk VY, Kasheva TN, Villa AE (2001).„Estimation of Aqueous Solubility of Chemical Compounds Using E-State Indices”.Chem Inf. Comput. Sci.41:1488—1493.PMID11749573.doi:10.1021/ci000392t.уреди
  6. ^Ertl P.; Rohde B.; Selzer P. (2000).„Fast calculation of molecular polar surface area as a sum of fragment based contributions and its application to the prediction of drug transport properties”.J. Med. Chem.43:3714—3717.PMID11020286.doi:10.1021/jm000942e.уреди
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