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Ketoprofen

Ketoprofen
Klinički podaci
Prodajno imeActron, Alrheumat, Alrheumun, Capisten
Drugs.comMonografija
Način primeneOralno
Farmakokinetički podaci
Poluvreme eliminacije1,1-4 h
IzlučivanjeRenalno (80%)
Identifikatori
CAS broj22071-15-4 ДаY
ATC kodM01AE03 (WHO), M02AA10
PubChemCID 3825
DrugBankDB01009 ДаY
ChemSpider3693 ДаY
KEGGC01716 ДаY
ChEBICHEBI:6128 ДаY
ChEMBLCHEMBL571 ДаY
Hemijski podaci
FormulaC16H14O3
Molarna masa254,281
  • CC(C(O)=O)C1=CC(=CC=C1)C(=O)C1=CC=CC=C1
  • InChI=1S/C16H14O3/c1-11(16(18)19)13-8-5-9-14(10-13)15(17)12-6-3-2-4-7-12/h2-11H,1H3,(H,18,19) ДаY
  • Key:DKYWVDODHFEZIM-UHFFFAOYSA-N ДаY
Fizički podaci
Tačka topljenja94 °C (201 °F)

Ketoprofen je organsko jedinjenje, koje sadrži 16 atoma ugljenika i ima molekulsku masu od 254,281 Da.[1][2][3][4]

Osobine

Osobina Vrednost
Broj akceptora vodonika 3
Broj donora vodonika 1
Broj rotacionih veza 4
Particioni koeficijent[5] (ALogP) 3,4
Rastvorljivost[6] (logS, log(mol/L)) -4,4
Polarna površina[7] (PSA, Å2) 54,4

Reference

  1. ^ Kantor TG: Ketoprofen: a review of its pharmacologic and clinical properties. Pharmacotherapy. 1986 May-Jun;6(3):93-103. PMID 3526298
  2. ^ Mazieres B: Topical ketoprofen patch. Drugs R D. 2005;6(6):337-44. PMID 16274258
  3. ^ 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. PMC 3013709Слободан приступ. PMID 21059682. doi:10.1093/nar/gkq1126.  уреди
  4. ^ David S. Wishart; Craig Knox; An Chi Guo; Dean Cheng; Savita Shrivastava; Dan Tzur; Bijaya Gautam; Murtaza Hassanali (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. Nucleic acids research. 36 (Database issue): D901—6. PMC 2238889Слободан приступ. PMID 18048412. doi:10.1093/nar/gkm958.  уреди
  5. ^ Ghose, A.K.; Viswanadhan V.N. & 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. 
  6. ^ 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. PMID 11749573. doi:10.1021/ci000392t.  уреди
  7. ^ 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. PMID 11020286. doi:10.1021/jm000942e.  уреди

Literatura

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