8-Azaguanin
8-Azaguanin je organsko jedinjenje, koje sadrži 4 atoma ugljenika i ima molekulsku masu od 152,114 Da.[3][4][5][6]
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| Identifikacija | |
|---|---|
3D model (Jmol)
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| ChEBI | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.004.681 |
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| Svojstva | |
| C4H4N6O | |
| Molarna masa | 152,114 |
| Tačka topljenja | 300 |
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |
 verifikuj (šta je   ?)
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| Reference infokutije | |
Osobine уреди
| Osobina | Vrednost |
|---|---|
| Broj akceptora vodonika | 6 |
| Broj donora vodonika | 3 |
| Broj rotacionih veza | 0 |
| Particioni koeficijent[7] (ALogP) | -0,1 |
| Rastvorljivost[8] (logS, log(mol/L)) | 0,3 |
| Polarna površina[9] (PSA, Å2) | 113,6 |
Reference уреди
- ^ 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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
- ^ 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.
- ^ Tong, George L.; Lee, William W.; Goodman, Leon; Frederiksen, Sune (1965). Synthesis of some 22-deoxyribosides of 8-azaadenine. Archives of Biochemistry and Biophysics (University of California: Elsevier) 112 (1): 76. Tong, George L.; Lee, William W.; Goodman, Leon; Frederiksen, Sune (1965). „Synthesis of some 2′-deoxyribosides of 8-azaadenine”. Archives of Biochemistry and Biophysics. 112: 76—81. doi:10.1016/0003-9861(65)90012-3. https://dx.doi.org/10.1016/0003-9861(65)90012-3
- ^ Michels AW, Ostrov DA, Zhang L, Nakayama M, Fuse M, McDaniel K, Roep BO, Gottlieb PA, Atkinson MA, Eisenbarth GS: Structure-based selection of small molecules to alter allele-specific MHC class II antigen presentation. J Immunol. 2011 Dec 1;187(11):5921-30. Epub 2011 Oct 31. . Michels, A. W.; Ostrov, D. A.; Zhang, L.; Nakayama, M.; Fuse, M.; McDaniel, K.; Roep, B. O.; Gottlieb, P. A.; Atkinson, M. A.; Eisenbarth, G. S. (2011). „Structure-based selection of small molecules to alter allele-specific MHC class II antigen presentation”. Journal of Immunology (Baltimore, Md. : 1950). 187 (11): 5921—5930. PMC 3221928
. PMID 22043012. doi:10.4049/jimmunol.1100746.
- ^ 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, A. C.; Wishart, D. S. (2011). „DrugBank 3.0: A comprehensive resource for 'omics' research on drugs”. Nucleic Acids Research. 39 (Database issue): D1035—41. PMC 3013709 . PMID 21059682. doi:10.1093/nar/gkq1126.
- ^ Wishart, D. S.; Knox, C.; Guo, A. C.; Cheng, D.; Shrivastava, S.; Tzur, D.; Gautam, B.; Hassanali, M. (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, I. V.; Tanchuk, V. Y.; Kasheva, T. N.; Villa, A. E. (2001). „Estimation of aqueous solubility of chemical compounds using E-state indices”. Journal of Chemical Information and Computer Sciences. 41 (6): 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”. Journal of Medicinal Chemistry. 43 (20): 3714—3717. PMID 11020286. doi:10.1021/jm000942e.
Literatura уреди
- Clayden, Jonathan; Greeves, Nick; Warren, Stuart; Wothers, Peter (2001). Organic Chemistry (I изд.). Oxford University Press. ISBN 978-0-19-850346-0.
- Smith, Michael B.; March, Jerry (2007). Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th изд.). New York: Wiley-Interscience. ISBN 0-471-72091-7.
- Katritzky A.R.; Pozharskii A.F. (2000). Handbook of Heterocyclic Chemistry (Second изд.). Academic Press. ISBN 0080429882.
