Ksantofil

Ksantofil
	; Ksantofil daje boju žumancetu
Nazivi
	IUPAC naziv 4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-(4-hidroksi-2,6,6-trimetilcikloheks-1-en-1-il)-3,7,12,16-tetrametiloktadeka-1,3,5,7,9,11,13,15,17-nonaen-1-il]-3,5,5-trimetilcikloheks-2-en-1-ol
Identifikacija
CAS broj	127-40-2 ;
3D model (Jmol)	Interactive image;
ChEBI	CHEBI:27325 ;
ChemSpider	4519703 ;
DrugBank	DB00137;
PubChem CID	5368396;
	SMILES C\C(\C=C\C=C(/C)\C=C\C1C(C)=CC(O)CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)CC(O)CC1(C)C;
Svojstva
Hemijska formula	C40H56O2
Molarna masa	568.8714
Tačka topljenja	196
Farmakologija
Načini upotrebe	Oralno
	Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25°C [77°F], 100 kPa).
	verifikuj (šta je ?)
	Reference infokutije

Ksantofili su žuti pigmenti iz karotenoidne grupe koji su široko rasprostanjeni u prirodi. Oni su između ostalog prisutni u žumancentu, algama, i laticama žutih cvetova. Ksantofili obuhvataju lutein, zeaksantin, neoksantin, violaksantin, i α- i β-kriptoksantin, od kojij je lutein primarno zastupljen u hrani.^[3]^[4]^[5]^[6]

ReferenceУреди

^ 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. уреди
^ 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.
^ Namitha KK, Negi PS: Chemistry and biotechnology of carotenoids. Crit Rev Food Sci Nutr. 2010 Sep;50(8):728-60. PMID 20830634
^ Ma L, Lin XM: Effects of lutein and zeaxanthin on aspects of eye health. J Sci Food Agric. 2010 Jan 15;90(1):2-12. PMID 20355006
^ 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 AC, Wishart DS (2011). „DrugBank 3.0: a comprehensive resource for omics research on drugs”. Nucleic Acids Res. 39 (Database issue): D1035—41. PMID 21059682.
^ Wishart DS, Knox C, Guo AC, Cheng D, Shrivastava S, Tzur D, Gautam B, Hassanali M (Nucleic Acids Res) (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. 36 (Database issue): D901—6. PMID 18048412.

Spoljašnje vezeУреди

Xanthophyll

Molimo Vas, obratite pažnju na važno upozorenje
u vezi sa temama iz oblasti medicine (zdravlja).

[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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

[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] Namitha KK, Negi PS: Chemistry and biotechnology of carotenoids. Crit Rev Food Sci Nutr. 2010 Sep;50(8):728-60. PMID 20830634

[4] Ma L, Lin XM: Effects of lutein and zeaxanthin on aspects of eye health. J Sci Food Agric. 2010 Jan 15;90(1):2-12. PMID 20355006

[5] 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 AC, Wishart DS (2011). „DrugBank 3.0: a comprehensive resource for omics research on drugs”. Nucleic Acids Res. 39 (Database issue): D1035—41. PMID 21059682.

[6] Wishart DS, Knox C, Guo AC, Cheng D, Shrivastava S, Tzur D, Gautam B, Hassanali M (Nucleic Acids Res) (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. 36 (Database issue): D901—6. PMID 18048412.

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[6]

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Nazivi

Ksantofil daje boju žumancetu
IUPAC naziv 4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-(4-hidroksi-2,6,6-trimetilcikloheks-1-en-1-il)-3,7,12,16-tetrametiloktadeka-1,3,5,7,9,11,13,15,17-nonaen-1-il]-3,5,5-trimetilcikloheks-2-en-1-ol
Identifikacija
CAS broj	127-40-2^Y
3D model (Jmol)	Interactive image
ChEBI	CHEBI:27325^Y
ChemSpider	4519703^Y
DrugBank	DB00137
PubChem^[1]^[2] CID	5368396

SMILES C\C(\C=C\C=C(/C)\C=C\C1C(C)=CC(O)CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)CC(O)CC1(C)C
Svojstva
Hemijska formula	C₄₀H₅₆O₂
Molarna masa	568.8714
Tačka topljenja	196
Farmakologija
Načini upotrebe	Oralno
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25°C [77°F], 100 kPa).
Y verifikuj (šta je ^YН ?)
Reference infokutije