Timin

Timin
	5-Metilpirimidin-2,4(1H,3H)-dion
Drugi nazivi	5-metiluracil
Identifikacija
CAS registarski broj	65-71-4
PubChem	1135
ChemSpider	1103
UNII	QR26YLT7LT
MeSH	Thymine
ChEBI	17821
ChEMBL	CHEMBL993
Jmol-3D slike	Slika 1
SMILES
	Cc1c[nH]c(=O)[nH]c1=O
InChI
	InChI=1S/C5H6N2O2/c1-3-2-6-5(9)7-4(3)8/h2H,1H3,(H2,6,7,8,9) ; Kod: RWQNBRDOKXIBIV-UHFFFAOYSA-N InChI=1/C5H6N2O2/c1-3-2-6-5(9)7-4(3)8/h2H,1H3,(H2,6,7,8,9); Kod: RWQNBRDOKXIBIV-UHFFFAOYAL
Svojstva
Molekulska formula	C5H6N2O2
Molarna masa	126.11 g mol−1
Gustina	1,23 g cm−3 (izračunata)
Tačka topljenja	316-317 °C, 589-590 K, 601-603 °F
Tačka ključanja	335 °C, 608 K, 635 °F (razlaže se)
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Timin, takođe poznat kao 5-metiluracil, je pirimidinska nukleobaza. Nalazi se u nukleinskoj kiselini DNK. U RNK timin zamenjuje uracil u većini slučajeva. Timin gradi bazni par sa adeninom.

Timin povezan sa dezoksiribozom gradi nukleozid timidin. Timidin se može vezati sa jednom, dve ili tri grupe fosforne kiseline, gradeći redom TMP, TDP or TTP (timidin mono- di- ili trifosfat).

Reference uredi

↑ 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.
↑ 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
↑ 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

Spoljašnje veze uredi

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Computational Chemistry Wiki Arhivirano 2006-06-29 na Wayback Machine-u

[1] 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

[2] 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.

[3] 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

[4] 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

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