Flurbiprofen
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| Klinički podaci | |||
|---|---|---|---|
| Robne marke | Adfeed, Ansaid, Antadys, Apo-Flurbiprofen | ||
| AHFS/Drugs.com | Monografija | ||
| Identifikatori | |||
| CAS broj | 5104-49-4 | ||
| ATC kod | M01AE09 , S01BC04 | ||
| PubChem[1][2] | 3394 | ||
| DrugBank | DB00712 | ||
| ChemSpider[3] | 3277 | ||
| ChEBI | CHEBI:5130 
| ||
| ChEMBL[4] | CHEMBL563
| ||
| Hemijski podaci | |||
| Formula | C15H13FO2 | ||
| Mol. masa | 244,261 | ||
| SMILES | eMolekuli & PubHem | ||
| |||
| Fizički podaci | |||
| Tačka topljenja | 110-111 °C (-58 °F) | ||
| Farmakokinetički podaci | |||
| Poluvreme eliminacije | 4,7 h | ||
| Izlučivanje | Renalno | ||
| Farmakoinformacioni podaci | |||
| Trudnoća | ? | ||
| Pravni status | |||
| Način primene | Oftalmički, oralno | ||
Flurbiprofen (po IUPACu 2-(3-fluoro-4-fenil-fenil)propionska kiselina) spada u grupu nesteroidnih antiupalnih lijekova. Hemijska formula mu je C15H13FO2. Spada u porodicu derivata fenilalkanoične kiseline. Upotrebljava se za ublažavanje upale i bola kod artritisa.[5][6] Također je poznat po trgovačkom imenu ANSAID kojeg proizvodi farmaceutska kompanija Pfizer.
R-flurbiprofen je jedini enantiomer flurbiprofena. Ovaj spoj se trenutno ispituje za upotrebu prilikom tretmana metastatičkog raka prostate i Alzheimerove bolesti.
Flurbiprofen je organsko jedinjenje, koje sadrži 15 atoma ugljenika i ima molekulsku masu od 244,261 Da.
Osobine[uredi | uredi kod]
| Osobina | Vrednost |
|---|---|
| Broj akceptora vodonika | 2 |
| Broj donora vodonika | 1 |
| Broj rotacionih veza | 3 |
| Particioni koeficijent[7] (ALogP) | 3,7 |
| Rastvorljivost[8] (logS, log(mol/L)) | -4,6 |
| Polarna površina[9] (PSA, Å2) | 37,3 |
Reference[uredi | uredi kod]
- ↑ 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.
- ↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594.
- ↑ 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 AC, Wishart DS (2011). „DrugBank 3.0: a comprehensive resource for omics research on drugs”. Nucleic Acids Res. 39 (Database issue): D1035-41. DOI:10.1093/nar/gkq1126. PMC 3013709. PMID 21059682.
- ↑ David S. Wishart, Craig Knox, An Chi Guo, Dean Cheng, Savita Shrivastava, Dan Tzur, Bijaya Gautam, and Murtaza Hassanali (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. Nucleic Acids Res 36 (Database issue): D901-6. DOI:10.1093/nar/gkm958. PMC 2238889. PMID 18048412.
- ↑ Ghose, A.K., Viswanadhan V.N., and Wendoloski, J.J. (1998). „Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragment Methods: An Analysis of AlogP and CLogP Methods”. J. Phys. Chem. A 102: 3762-3772. DOI:10.1021/jp980230o.
- ↑ Tetko IV, Tanchuk VY, Kasheva TN, Villa AE. (2001). „Estimation of Aqueous Solubility of Chemical Compounds Using E-State Indices”. Chem Inf. Comput. Sci. 41: 1488-1493. DOI:10.1021/ci000392t. PMID 11749573.
- ↑ 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”. J. Med. Chem. 43: 3714-3717. DOI:10.1021/jm000942e. PMID 11020286.
Literatura[uredi | uredi kod]
- Hardman JG, Limbird LE, Gilman AG. (2001). Goodman & Gilman's The Pharmacological Basis of Therapeutics (10 izd.). New York: McGraw-Hill. DOI:10.1036/0071422803. ISBN 0-07-135469-7.
- Thomas L. Lemke, David A. Williams, ur. (2007). Foye's Principles of Medicinal Chemistry (6 izd.). Baltimore: Lippincott Willams & Wilkins. ISBN 0-7817-6879-9.
