Rivastigmin
Изглед
(преусмерено са Exelon)
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Klinički podaci | |
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Prodajno ime | Exelon, Exelon Patch |
Drugs.com | Monografija |
Način primene | Oralno |
Farmakokinetički podaci | |
Poluvreme eliminacije | 1,5 h |
Identifikatori | |
CAS broj | 123441-03-2 ![]() |
ATC kod | N06DA03 (WHO) |
PubChem | CID 77991 |
DrugBank | DB00989 ![]() |
ChemSpider | 70377 ![]() |
KEGG | C11766 ![]() |
ChEMBL | CHEMBL636 ![]() |
Hemijski podaci | |
Formula | C14H22N2O2 |
Molarna masa | 250,337 |
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Rivastigmin je organsko jedinjenje, koje sadrži 14 atoma ugljenika i ima molekulsku masu od 250,337 Da.[1][2][3][4][5]
Osobine
[уреди | уреди извор]Osobina | Vrednost |
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Broj akceptora vodonika | 3 |
Broj donora vodonika | 0 |
Broj rotacionih veza | 5 |
Particioni koeficijent[6] (ALogP) | 2,6 |
Rastvorljivost[7] (logS, log(mol/L)) | -2,4 |
Polarna površina[8] (PSA, Å2) | 32,8 |
Reference
[уреди | уреди извор]- ^ Camps, P.; Muñoz-Torrero, D. (фебруар 2002). „Cholinergic drugs in pharmacotherapy of Alzheimer's disease”. Mini Reviews in Medicinal Chemistry. 2 (1): 11—25. PMID 12369954. doi:10.2174/1389557023406638.
- ^ Rosler, M.; Anand, R.; Cicin-Sain, A.; Gauthier, S.; Agid, Y.; Dal-Bianco, P.; Stahelin, H. B.; Hartman, R.; Gharabawi, M.; Bayer, T. (март 1999). „Efficacy and safety of rivastigmine in patients with Alzheimer's disease: International randomised controlled trial Commentary: Another piece of the Alzheimer's jigsaw”. BMJ. 318 (7184): 633—8. PMC 27767
. PMID 10066203. doi:10.1136/bmj.318.7184.633.
- ^ Finkel, S. I. (јул 2004). „Effects of rivastigmine on behavioral and psychological symptoms of dementia in Alzheimer's disease”. Clinical Therapeutics. 26 (7): 980—90. PMID 15336465. doi:10.1016/s0149-2918(04)90172-5.
- ^ 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 3013709
. PMID 21059682. doi:10.1093/nar/gkq1126.
- ^ 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 2238889
. PMID 18048412. doi:10.1093/nar/gkm958.
- ^ 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.
- ^ 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.
- ^ 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
[уреди | уреди извор]- Hardman JG, Limbird LE, Gilman AG (2001). Goodman & Gilman's The Pharmacological Basis of Therapeutics (10. изд.). New York: McGraw-Hill. ISBN 0071354697. doi:10.1036/0071422803.
- Thomas L. Lemke; David A. Williams, ур. (2007). Foye's Principles of Medicinal Chemistry (6. изд.). Baltimore: Lippincott Willams & Wilkins. ISBN 0781768799.
Spoljašnje veze
[уреди | уреди извор]
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