Etosuksimid je organsko jedinjenje, koje sadrži 7 atoma ugljenika i ima molekulsku masu od 141,168 Da.[1][2][3][4][5][6][7]
Osobine
Stereohemija
Ethosuksimid je hiralni lek s stereocenterom. Terapeutski se koristi racemat, 1: 1 smeša ( S ) i ( R ) izomera.[11]
Enantiomeri etosuksimida
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 CAS-Nummer: 39122-20-8
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 CAS-Nummer: 39122-19-5
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Reference
- ^ Patsalos PN: Properties of antiepileptic drugs in the treatment of idiopathic generalized epilepsies. Epilepsia. 2005;46 Suppl 9:140-8. . PMID 16302888.
- ^ Coulter DA, Huguenard JR, Prince DA (март 1989). „Specific petit mal anticonvulsants reduce calcium currents in thalamic neurons”. Neurosci Lett. 98 (1): 74—8. PMID 2710401.
- ^ Coulter DA, Huguenard JR, Prince DA (јун 1989). „Characterization of ethosuximide reduction of low-threshold calcium current in thalamic neurons”. Ann Neurol. 25 (6): 582—93. PMID 2545161.
- ^ Coulter DA, Huguenard JR, Prince DA (август 1990). „Differential effects of petit mal anticonvulsants and convulsants on thalamic neurones: calcium current reduction”. Br J Pharmacol. 100 (4): 800—6. PMID 2169941.
- ^ Kostyuk PG, Molokanova EA, Pronchuk NF, Savchenko AN, Verkhratsky AN: Different action of ethosuximide on low- and high-threshold calcium currents in rat sensory neurons. Neuroscience. . 51 (4). децембар 1992: 755—8. PMID 1336826.
- ^ 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—D1041. PMC 3013709
. PMID 21059682. doi:10.1093/nar/gkq1126.
- ^ Wishart, David S.; Knox, Craig; Guo, An Chi; Cheng, Dean; Shrivastava, Savita; Tzur, Dan; Gautam, Bijaya; Hassanali, Murtaza (2008). „DrugBank: A knowledgebase for drugs, drug actions and drug targets”. Nucleic Acids Research. 36 (Database issue): D901—D906. 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, 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.
- ^ 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.
- ^ Rote Liste Service GmbH (ed): Rote Liste 2017 – Arzneimittelverzeichnis für Deutschland (einschließlich EU-Zulassungen und bestimmter Medizinprodukte). Rote Liste Service GmbH, Frankfurt/Main, 2017, Aufl. 57, ISBN 978-3-946057-10-9, S. 182.
Literatura
Spoljašnje veze
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