Kalendinska kiselina

Kalendinska kiselina
	(8E,10E,12Z)-oktadeka-8,10,12-trienoinska kiselina
Drugi nazivi	alfa-kalendinska kiselina, 8E,10E,12Z-oktadekatrienoinska kiselina, trans-8-trans-10-cis-12-oktadekatrienoinska kiselina
Identifikacija
CAS registarski broj	5204-87-5
PubChem	5282818
ChemSpider	4445945
Jmol-3D slike	Slika 1
SMILES
	O=C(O)CCCCCC\C=C\C=C\C=C/CCCCC
InChI
	InChI=1S/C18H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h6-11H,2-5,12-17H2,1H3,(H,19,20)/b7-6-,9-8+,11-10+ ; Kod: DQGMPXYVZZCNDQ-KBPWROHVSA-N InChI=1/C18H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h6-11H,2-5,12-17H2,1H3,(H,19,20)/b7-6-,9-8+,11-10+; Kod: DQGMPXYVZZCNDQ-KBPWROHVBR
Svojstva
Molekulska formula	C18H30O2
Molarna masa	278.43 g mol−1
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Kalendinska kiselina (α-kalendinska kiselina) je nezasićena masna kiselina, koja je dobila ime po biljci Calendula officinalis (rod Calendula), iz koje je dobijena. Ona je hemijski slična sa konjugovanim linolnim kiselinama.^[4]

Biosinteza

Kalendinska kiselina je omega-6 masna kiselina,^[5] mada se obično ne svrstava u tu grupu.

Kalendinska kiselina se sintetiše u Calendula officinalis iz linoleata posredstvom neobične Δ12-oleat desaturaze (FAD 2 varijante) koja konvertuje cis-dvostruku vezu u poziciji 9 do trans,trans-konjugovanog sistema dvostrukih veza.^[6] Sve-trans beta izomer je takođe poznat.^[4]

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.
↑ 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
↑ ^4,0 ^4,1 Yasui Y, Hosokawa M, Kohno H, Tanaka T, Miyashita K (2006). „Growth inhibition and apoptosis induction by all-trans-conjugated linolenic acids on human colon cancer cells”. Anticancer Res 26 (3A): 1855–60. PMID 16827117.
↑ Kinney, Tony. „Metabolism in Plants to Produce Healthier Food Oils” (PDF). Arhivirano iz originala na datum 2006-09-29. Pristupljeno 11. 01. 2007.
↑ Christie, William W. „Fatty Acids: Polyunsaturated with other than Methylene-Interrupted Double Bonds”. Lipid Library. Pristupljeno 11. 01. 2007.

Spoljašnje veze

Portal Hemija

[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

[Yasui-4] 4,0 ^4,1 Yasui Y, Hosokawa M, Kohno H, Tanaka T, Miyashita K (2006). „Growth inhibition and apoptosis induction by all-trans-conjugated linolenic acids on human colon cancer cells”. Anticancer Res 26 (3A): 1855–60. PMID 16827117.

[Kinney-5] Kinney, Tony. „Metabolism in Plants to Produce Healthier Food Oils” (PDF). Arhivirano iz originala na datum 2006-09-29. Pristupljeno 11. 01. 2007.

[lipd_library-6] Christie, William W. „Fatty Acids: Polyunsaturated with other than Methylene-Interrupted Double Bonds”. Lipid Library. Pristupljeno 11. 01. 2007.

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