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Vitamin D5
	(1S,3Z)-3-[(2E)-2-[(1R,3aS,7aR)-1-[(1R,4S)-4-etil-1,5-dimetilheksil]-7a-metil-2,3,3a,5,6,7-heksahidro-1H-inden-4-iliden]etiliden]-4-metilen-1-cikloheksanol
Identifikacija
CAS registarski broj	71761-06-3
PubChem	9547700
ChemSpider	7826639
Jmol-3D slike	Slika 1
SMILES
	O[C@@H]1CC(\C(=C)CC1)=C\C=C2/CCC[C@]3([C@H]2CC[C@@H]3[C@H](C)CC[C@H](CC)C(C)C)C
InChI
	InChI=1S/C29H48O/c1-7-23(20(2)3)12-10-22(5)27-16-17-28-24(9-8-18-29(27,28)6)13-14-25-19-26(30)15-11-21(25)4/h13-14,20,22-23,26-28,30H,4,7-12,15-19H2,1-3,5-6H3/b24-13+,25-14-/t22-,23+,26+,27-,28+,29-/m1/s1 ; Kod: RMDJVOZETBHEAR-GHTRHTQZSA-N InChI=1/C29H48O/c1-7-23(20(2)3)12-10-22(5)27-16-17-28-24(9-8-18-29(27,28)6)13-14-25-19-26(30)15-11-21(25)4/h13-14,20,22-23,26-28,30H,4,7-12,15-19H2,1-3,5-6H3/b24-13+,25-14-/t22-,23+,26+,27-,28+,29-/m1/s1; Kod: RMDJVOZETBHEAR-GHTRHTQZBN
Svojstva
Molekulska formula	C29H48O
Molarna masa	412,69
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Vitamin D₅ je oblik vitamina D.

Analogna jedinjenja su predložena za upotrebu kao antitumorski agensi.^[4]^[5]^[6]

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
↑ Mehta RG, Moriarty RM, Mehta RR, et al. (February 1997). „Prevention of preneoplastic mammary lesion development by a novel vitamin D analogue, 1alpha-hydroxyvitamin D5”. J. Natl. Cancer Inst. 89 (3): 212–8. DOI:10.1093/jnci/89.3.212. PMID 9017001.
↑ Murillo G, Mehta RG (October 2005). „Chemoprevention of chemically-induced mammary and colon carcinogenesis by 1alpha-hydroxyvitamin D5”. J. Steroid Biochem. Mol. Biol. 97 (1-2): 129–36. DOI:10.1016/j.jsbmb.2005.06.008. PMID 16051482.
↑ Mehta RG (October 2004). „Stage-specific inhibition of mammary carcinogenesis by 1alpha-hydroxyvitamin D5”. Eur. J. Cancer 40 (15): 2331–7. DOI:10.1016/j.ejca.2004.05.025. PMID 15454260.