Temokapril
(IUPAC) ime | |||
---|---|---|---|
[(2S)-6[(1S)-1-(etoksikarbonil)-3-fenilpropil]amino5-okso-2-(2-tienil)-1,4-tiazepan-4-il]sirćetna kiselina | |||
Klinički podaci | |||
AHFS/Drugs.com | Internacionalno ime leka | ||
Identifikatori | |||
CAS broj | 111902-57-9 | ||
ATC kod | C09AA14 | ||
PubChem[1][2] | 71323 | ||
UNII | 18IZ008EU6 Y | ||
KEGG[3] | D08566 Y | ||
Hemijski podaci | |||
Formula | C23H28N2O5S2 | ||
Mol. masa | 476,608 g/mol | ||
SMILES | eMolekuli & PubHem | ||
| |||
Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status |
Temokapril (Temokaprilum, Acecol) je ACE inhibitor.[4] On nije odobren za upotrebu u SAD.
Osobine
Osobina | Vrednost |
---|---|
Broj akceptora vodonika | 7 |
Broj donora vodonika | 2 |
Broj rotacionih veza | 11 |
Particioni koeficijent[5] (ALogP) | 0,8 |
Rastvorljivost[6] (logS, log(mol/L)) | -5,6 |
Polarna površina[7] (PSA, Å2) | 149,5 |
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.
- ↑ Hisao Oguchi1, Masuo Tokoo, Shinichi Tokunaga, Makoto Higuchi, Kazuhiko Hora, Seiichi Furuta (1995). Temocapril, A Novel Angiotensin-Converting Enzyme Inhibitor with Preferential Biliary Excretion. 13. pp. 66–85. DOI:10.1111/j.1527-3466.1995.tb00214.x.
- ↑ 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. edit
- ↑ 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. edit
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 |
Temokapril na Wikimedijinoj ostavi
- Temocapril
- p
- r
- u
("-pril")
Sulfhidril: Kaptopril • Zofenopril
Dikarboksilat: Enalapril# • Ramipril • Kvinapril • Perindopril • Lisinopril • Benazepril
Ostali/negrupisani: Alacepril • Cilazapril • Delapril • Imidapril • Moeksipril • Rentiapril • Spirapril • Temokapril • Trandolapril("-sartan")
Azilsartan • Kandesartan • Eprosartan • Irbesartan • Losartan • Olmesartan • Tasosartan • Telmisartan • Valsartan
("-kiren")
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