Metronidazol
Изглед
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Klinički podaci | |
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Prodajno ime | Orvagil, Metronidazol |
Drugs.com | Monografija |
Način primene | Oralno, intravaginalno, topikalno |
Farmakokinetički podaci | |
Poluvreme eliminacije | 6-8 h |
Identifikatori | |
CAS broj | 443-48-1 ![]() |
ATC kod | A01AB17 (WHO), P01AB01 |
PubChem | CID 4173 |
DrugBank | DB00916 ![]() |
ChemSpider | 4029 ![]() |
ChEBI | CHEBI:6909 ![]() |
ChEMBL | CHEMBL137 ![]() |
Hemijski podaci | |
Formula | C6H9N3O3 |
Molarna masa | 171,154 |
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Fizički podaci | |
Tačka topljenja | 1.605 °C (2.921 °F) |
Metronidazol je organsko jedinjenje, koje sadrži 6 atoma ugljenika i ima molekulsku masu od 171,154 Da.[1][2][3][4][5][6]
Osobine
[уреди | уреди извор]Osobina | Vrednost |
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Broj akceptora vodonika | 4 |
Broj donora vodonika | 1 |
Broj rotacionih veza | 3 |
Particioni koeficijent[7] (ALogP) | -0,3 |
Rastvorljivost[8] (logS, log(mol/L)) | -1,3 |
Polarna površina[9] (PSA, Å2) | 83,9 |
Reference
[уреди | уреди извор]- ^ Shennan A, Crawshaw S, Briley A, Hawken J, Seed P, Jones G, Poston L (јануар 2006). „A randomised controlled trial of metronidazole for the prevention of preterm birth in women positive for cervicovaginal fetal fibronectin: the PREMET Study. BJOG”. 113 (1): 65—74. PMID 16398774.
- ^ Lamont RF: Can antibiotics prevent preterm birth--the pro and con debate. BJOG. 2005 Mar;112 Suppl. 1 67–73
- ^ Williams CS, Woodcock KR (фебруар 2000). „Do ethanol and metronidazole interact to produce a disulfiram-like reaction? Ann Pharmacother”. 34 (2): 255—7. PMID 10676835.
- ^ Visapaa JP, Tillonen JS, Kaihovaara PS, Salaspuro MP (јун 2002). „Lack of disulfiram-like reaction with metronidazole and ethanol. Ann Pharmacother”. 36 (6): 971—4. PMID 12022894.
- ^ 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 3013709
. PMID 21059682. doi:10.1093/nar/gkq1126.
- ^ 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 2238889
. PMID 18048412. doi:10.1093/nar/gkm958.
- ^ 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.
- ^ 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.
- ^ 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.
Literatura
[уреди | уреди извор]- Hardman JG, Limbird LE, Gilman AG (2001). Goodman & Gilman's The Pharmacological Basis of Therapeutics (10. изд.). New York: McGraw-Hill. ISBN 0071354697. doi:10.1036/0071422803.
- Thomas L. Lemke; David A. Williams, ур. (2007). Foye's Principles of Medicinal Chemistry (6. изд.). Baltimore: Lippincott Willams & Wilkins. ISBN 0781768799.
Spoljašnje veze
[уреди | уреди извор]
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