Gabapentin

Gabapentin
Klinički podaci
Prodajno imeAclonium, Neurontin, Novo-Gabapentin
Drugs.comMonografija
Način primeneOralno
Identifikatori
CAS broj60142-96-3 Зелена квачицаДа
ATC kodN03AX12 (WHO)
PubChemCID 3446
DrugBankDB00996 Зелена квачицаДа
ChemSpider3328 Зелена квачицаДа
ChEMBLCHEMBL940 Зелена квачицаДа

Gabapentin je organsko jedinjenje, koje sadrži 9 atoma ugljenika i ima molekulsku masu od 171,237 Da.[1][2][3][4][5][6][7][8][9]

Osobine

Osobina Vrednost
Broj akceptora vodonika 3
Broj donora vodonika 2
Broj rotacionih veza 3
Particioni koeficijent[10] (ALogP) -1,5
Rastvorljivost[11] (logS, log(mol/L)) -2,0
Polarna površina[12] (PSA, Å2) 63,3

Reference

  1. ^ Mathew, N. T.; Rapoport, A.; Saper, J.; Magnus, L.; Klapper, J.; Ramadan, N.; Stacey, B.; Tepper, S. (фебруар 2001). „Efficacy of gabapentin in migraine prophylaxis”. Headache.. 41 (2): 119—28. PMID 11251695. doi:10.1046/j.1526-4610.2001.111006119.x. 
  2. ^ Backonja, M. M.; Serra, J. (2004). „Pharmacologic management part 1: Better-studied neuropathic pain diseases”. Pain Medicine (Malden, Mass.). 5 Suppl 1: S28—47. PMID 14996228. doi:10.1111/j.1526-4637.2004.04020.x. 
  3. ^ Choudhuri, I.; Sarvananthan, N.; Gottlob, I. (септембар 2007). „Survey of management of acquired nystagmus in the United Kingdom”. Eye. 21 (9): 1194—7. PMID 16732211. doi:10.1038/sj.eye.6702434. 
  4. ^ Pande, A. C.; Crockatt, J. G.; Janney, C. A.; Werth, J. L.; Tsaroucha, G. (2000). „Gabapentin in bipolar disorder: A placebo-controlled trial of adjunctive therapy. Gabapentin Bipolar Disorder Study Group”. Bipolar Disorders. 2 (3 Pt 2): 249—255. PMID 11249802. doi:10.1034/j.1399-5618.2000.20305.x. 
  5. ^ Su, T. Z.; Feng, M. R.; Weber ML. (јун 2005). „Mediation of highly concentrative uptake of pregabalin by L-type amino acid transport in Chinese hamster ovary and Caco-2 cells.”. J Pharmacol Exp Ther.. 313 (3): 1406—15. PMID 15769862. doi:10.1124/jpet.104.082255. . Epub 2005 Mar 15. .
  6. ^ 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, A. C.; Wishart, D. S. (2011). „DrugBank 3.0: A comprehensive resource for 'omics' research on drugs”. Nucleic Acids Research. 39 (Database issue): D1035—41. PMC 3013709Слободан приступ. PMID 21059682. doi:10.1093/nar/gkq1126. 
  7. ^ Wishart, D. S.; Knox, C.; Guo, A. C.; Cheng, D.; Shrivastava, S.; Tzur, D.; Gautam, B.; Hassanali, M. (2008). „DrugBank: A knowledgebase for drugs, drug actions and drug targets”. Nucleic Acids Research. 36 (Database issue): D901—6. PMC 2238889Слободан приступ. PMID 18048412. doi:10.1093/nar/gkm958. 
  8. ^ Khademi S, Ghaffarpasand F, Heiran HR, Asefi A (2010). „Effects of preoperative gabapentin on postoperative nausea and vomiting after open cholecystectomy: A prospective randomized double-blind placebo-controlled study”. Med Princ Pract. 19 (1): 57—60. PMID 19996621. doi:10.1159/000252836. 
  9. ^ Bashir F, Bhat KM, Qazi S, Hashia AM (2009). „A randomized, double blind, placebo controlled study evaluating preventive role of gabapentin for PONV in patients undergoing laparascopic cholecystectomy”. JK Sci. 11: 190—3. 
  10. ^ Ghose, Arup K.; Viswanadhan, Vellarkad N.; Wendoloski, John J. (1998). „Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragmental Methods: An Analysis of ALOGP and CLOGP Methods”. The Journal of Physical Chemistry A. 102 (21): 3762—3772. Bibcode:1998JPCA..102.3762G. doi:10.1021/jp980230o. 
  11. ^ Tetko, I. V.; Tanchuk, V. Y.; Kasheva, T. N.; Villa, A. E. (2001). „Estimation of aqueous solubility of chemical compounds using E-state indices”. Journal of Chemical Information and Computer Sciences. 41 (6): 1488—1493. PMID 11749573. doi:10.1021/ci000392t. 
  12. ^ 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”. Journal of Medicinal Chemistry. 43 (20): 3714—3717. PMID 11020286. doi:10.1021/jm000942e. 

Literatura

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