Zotarolimus
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Klinički podaci | |||
---|---|---|---|
AHFS/Drugs.com | Monografija | ||
Identifikatori | |||
CAS broj | 221877-54-9 | ||
ATC kod | nije dodeljen | ||
ChemSpider[1] | 21468821 | ||
UNII | H4GXR80IZE ![]() | ||
KEGG[2] | D06669 ![]() | ||
ChEMBL[3] | CHEMBL1614661 ![]() | ||
Hemijski podaci | |||
Formula | C52H79N5O12 | ||
Mol. masa | 966,210 | ||
SMILES | eMolekuli & PubHem | ||
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Sinonimi | (42S)-42-Deoxy-42-(1H-tetrazol-1-yl)-rapamycin | ||
Fizički podaci | |||
Rastvorljivost u voda | sciencedirect.com /> mg/mL (20 °C) | ||
Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status |
Zotarolimus je organsko jedinjenje, koje sadrži 52 atoma ugljenika i ima molekulsku masu od 966,210 Da.
Osobine
Osobina | Vrednost |
---|---|
Broj akceptora vodonika | 15 |
Broj donora vodonika | 2 |
Broj rotacionih veza | 7 |
Particioni koeficijent[4] (ALogP) | 5,8 |
Rastvorljivost[5] (logS, log(mol/L)) | -11,1 |
Polarna površina[6] (PSA, Å2) | 218,8 |
Reference
- ↑ 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. edit
- ↑ 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 |
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Zotarolimus na Wikimedijinoj ostavi
- Zotarolimus