Flunoksaprofen
Klinički podaci | |||
---|---|---|---|
AHFS/Drugs.com | Monografija | ||
Identifikatori | |||
CAS broj | 66934-18-7 | ||
ATC kod | G02CC04 M01AE15 | ||
PubChem[1][2] | 68869 | ||
UNII | UKU5U19W9M Y | ||
KEGG[3] | D07219 Y | ||
ChEMBL[4] | CHEMBL1614641 Y | ||
Hemijski podaci | |||
Formula | C16H12FNO3 | ||
Mol. masa | 285,270 | ||
SMILES | eMolekuli & PubHem | ||
| |||
Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status |
Flunoksaprofen je organsko jedinjenje, koje sadrži 16 atoma ugljenika i ima molekulsku masu od 285,270 Da.
Osobine
Osobina | Vrednost |
---|---|
Broj akceptora vodonika | 3 |
Broj donora vodonika | 1 |
Broj rotacionih veza | 3 |
Particioni koeficijent[5] (ALogP) | 3,6 |
Rastvorljivost[6] (logS, log(mol/L)) | -5,0 |
Polarna površina[7] (PSA, Å2) | 63,3 |
Reference
- ↑ 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. edit
- ↑ 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.
- ↑ 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.
- ↑ 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. edit
- ↑ 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
- 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.
Spoljašnje veze
Portal Medicina | |
Portal Hemija |
Flunoksaprofen na Wikimedijinoj ostavi
- Flunoxaprofen
- p
- r
- u
Diklofenak • Aceklofenak • Acemetacin • Alklofenak • Bromfenak • Etodolak • Indometacin • Indometacin farnesil • Nabumeton • Oksametacin • Proglumetacin • Sulindac • Tolmetin
(profeni)
Ibuprofen • Alminoprofen • Benoksaprofen • Karprofen • Deksibuprofen • Deksketoprofen • Fenbufen • Fenoprofen • Flunoksaprofen • Flurbiprofen • Ibuproksam • Indoprofen† • Ketoprofen • Ketorolak • Loksoprofen • Miroprofen • Naproksen • Oksaprozin • Pirprofen • Suprofen • Tarenflurbil • Tiaprofenska kiselina
(fenaminske kiseline)
Fenilbutazon • Ampiron • Azapropazon • Klofezon • Kebuzon • Metamizol • Mofebutazon • Oksifenbutazon • Fenazon • Sulfinpirazon
Celekoksib • Derakoksib‡ • Etorikoksib • Firokoksib‡ • Lumirakoksib† • Parekoksib • Rofekoksib† • Valdekoksib†
Bendazac • Diklofenak • Etofenamat • Felbinak • Flurbiprofen • Ibuprofen • Indometacin • Ketoprofen • Naproksen • Piroksikam • Suprofen
Podebljani nazivi označavaju jedinjenja (spojeve) inicijalno razvijene u specifičnim grupama. †Lekovi povučeni sa tržišta. ‡Veterinarski lekovi.