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Iloperidon

С Википедије, слободне енциклопедије
Iloperidon
Klinički podaci
Prodajno imeFanapt, Fiapta, Zomaril
Drugs.comMonografija
Način primeneOralno
Identifikatori
CAS broj133454-47-4 Зелена квачицаДа
ATC kodN05AX14 (WHO)
PubChemCID 71360
DrugBankDB04946 Зелена квачицаДа
ChemSpider64459 Зелена квачицаДа
ChEMBLCHEMBL14376 Зелена квачицаДа

Iloperidon je organsko jedinjenje, koje sadrži 24 atoma ugljenika i ima molekulsku masu od 426,481 Da.[1][2][3][4][5][6][7][8][9]

Osobina Vrednost
Broj akceptora vodonika 5
Broj donora vodonika 0
Broj rotacionih veza 8
Particioni koeficijent[10] (ALogP) 4,0
Rastvorljivost[11] (logS, log(mol/L)) -6,3
Polarna površina[12] (PSA, Å2) 64,8
  1. ^ Strupczewski, J. T.; Bordeau, K. J.; Chiang, Y.; Glamkowski, E. J.; Conway, P. G.; Corbett, R.; Hartman, H. B.; Szewczak, M. R.; Wilmot, C. A.; Helsley, G. C. (1995). . „3-(Aryloxy)alkylpiperidinyl-1,2-benzisoxazoles as D2/5-HT2 antagonists with potential atypical antipsychotic activity: Antipsychotic profile of iloperidone (HP 873)”. Journal of Medicinal Chemistry. 38 (7): 1119—1131. PMID 7707315. doi:10.1021/jm00007a009. 
  2. ^ Kongsamut, S.; Roehr, J. E.; Cai, J.; Hartman, H. B.; Weissensee, P.; Kerman, L. L.; Tang, L.; Sandrasagra, A. (1996). . „Iloperidone binding to human and rat dopamine and 5-HT receptors”. Eur J Pharmacol. 317 (2–3): 417—423. PMID 8997630. doi:10.1016/s0014-2999(96)00840-0. 
  3. ^ Hesselink, J. M. (2002). . „Iloperidone (Novartis)”. Idrugs : The Investigational Drugs Journal. 5 (1): 84—90. PMID 12861482. 
  4. ^ Hesselink, J. M. (1999). . „Iloperidone (Hoechst Marion Roussel Inc)”. Idrugs : The Investigational Drugs Journal. 2 (6): 584—590. PMID 16127622. 
  5. ^ Szewczak, M. R.; Corbett, R.; Rush, D. K.; Wilmot, C. A.; Conway, P. G.; Strupczewski, J. T.; Cornfeldt, M. (1995). . „The pharmacological profile of iloperidone, a novel atypical antipsychotic agent”. J Pharmacol Exp Ther. 274 (3): 1404—1413. PMID 7562515. doi:10.1016/S0022-3565(25)10685-X. 
  6. ^ Bobo, W. V. (2013). . „Asenapine, iloperidone and lurasidone: Critical appraisal of the most recently approved pharmacotherapies for schizophrenia in adults”. Expert Review of Clinical Pharmacology. 6 (1): 61—91. PMID 23272794. doi:10.1586/ecp.12.70. 
  7. ^ Citrome, L. (2010). . „Iloperidone: Chemistry, pharmacodynamics, pharmacokinetics and metabolism, clinical efficacy, safety and tolerability, regulatory affairs, and an opinion”. Expert Opinion on Drug Metabolism & Toxicology. 6 (12): 1551—1564. PMID 21034370. doi:10.1517/17425255.2010.531259. 
  8. ^ 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. 
  9. ^ 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. 
  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, Igor V.; Tanchuk, Vsevolod Yu.; Kasheva, Tamara N.; Villa, Alessandro E. P. (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, Peter; Rohde, Bernhard; Selzer, Paul (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. 

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