Dihidrofolna kiselina

Dihidrofolna kiselina
	N-(4[(2-amino-4-okso-1,4,7,8-tetrahidropteridin-6-il)metil]amino
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

benzoil)-L-glutaminska kiselina

| OtherNames = H₂folat, DH | Section1 = ! align="center" cellspacing="3" style="border: 1px solid #C0C090; background-color: #F8EABA; margin-bottom: 3px;" colspan="2" | Identifikacija |-

| CAS registarski broj | 4033-27-6 |-

| PubChem^[1]^[2] | 98792 |-

| ChemSpider^[3] | 89228^Y |-

| MeSH | dihydrofolate |- | ChEBI | 15633 |-

| ChEMBL^[4] | {{#if:46294|CHEMBL46294^Y |-

| Jmol-3D slike | {{#if:O=C(O)[C@@H](NC(=O)c1ccc(cc1)NCC/2=N/C=3C(=O)\N=C(/NC=3NC\2)N)CCC(=O)O|Slika 1 |-

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|- | Section2 = ! align="center" cellspacing="3" style="border: 1px solid #C0C090; background-color: #F8EABA; margin-bottom: 3px;" colspan="2" | Svojstva |- | Molekulska formula | C₁₉H₂₁N₇O₆ |- | Molarna masa | 443,414 g/mol |- | Section3 = }}

Dihidrofolna kiselina (dihidrofolat, vitamin B₉) je derivat folne kiseline koji se konvertuje u tetrahidrofolnu kiselinu posredstvom dihidrofolatne reduktaze. Tetrahidrofolat je neophodan za formiranje purina i pirimidina, koji su gradivni blokovi DNK i RNK. Dihidrofolat reduktaza je meta lekova koji sprečavaju sintezu nukleinskih kiselina.^[5]

↑ 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
↑ E. L R. Stokstad and T. H. Jukes (1987). „Sulfonamides and Folie Acid Antagonists: A Historical Review”. J. Nutr. 117: 1335-1341.

[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

[5] E. L R. Stokstad and T. H. Jukes (1987). „Sulfonamides and Folie Acid Antagonists: A Historical Review”. J. Nutr. 117: 1335-1341.

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Dihidrofolna kiselina

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