Etilevodopa
Etilevodopa je dopaminergički agens koji se koristi za lečenje Parkinsonove bolesti.[5] Ovo jedinjenje je etil estar levodope.
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(IUPAC) ime | |||
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etil (2S)-2-amino-3-(3,4-dihidroksifenil)propanoat | |||
Klinički podaci | |||
Identifikatori | |||
CAS broj | 37178-37-3 | ||
ATC kod | N04BA06 | ||
PubChem[1][2] | 170345 | ||
ChemSpider[3] | 148944 | ||
UNII | 895X917GYE ![]() | ||
KEGG[4] | D04097 ![]() | ||
Hemijski podaci | |||
Formula | C11H15NO4 | ||
Mol. masa | 225,241 g/mol | ||
SMILES | eMolekuli & PubHem | ||
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Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status |
Reference Uredi
- ↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519.
- ↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
- ↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846.
- ↑ Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
- ↑ Djaldetti Ruth, Giladi Nir, Hassin-Baer Sharon, Shabtai Hertzel, Melamed Eldad (November 2003). „Pharmacokinetics of Etilevodopa Compared to Levodopa in Patient's With Parkinson's Disease: An Open-label, Randomized, Crossover Study”. Clinical Neuropharmacology 26 (6): 322-326.