24,25-Dihidroksiholekalciferol

24,25-Dihidroksiholekalciferol
Nazivi
	IUPAC naziv (6R)-6-[(1R,3aS,4E,7aR)-4-[(2Z)-2-[(5S)-5-hidroksi-2-metilencikloheksiliden]etiliden]-7a-metil-2,3,3a,5,6,7-heksahidro-1H-inden-1-il]-2-metilheptan-2,3-diol
	Drugi nazivi 24,25-dihidroksivitamin D3; (24R)-hidroksikalcifediol; (24R)-hidroksikalcidiol
Identifikacija
CAS broj	40013-87-4 ;
3D model (Jmol)	interaktivna slika;
ChemSpider	4939193 ;
ECHA InfoCard	100.049.754
PubChem C ID	6434253;
	SMILES O[C@@H]1CC(\C(=C)CC1)=C\C=C2/CCC[C@]3([C@H]2CC[C@@H]3[C@H](C)CCC(O)C(O)(C)C)C; ; ; ; ; ;
Svojstva
Hemijska formula	C27H44O3
Molarna masa	416,63 g/mol
	Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
	verifikuj (šta je ?)
	Reference infokutije

24,25-Dihidroksiholekalciferol (24,25-dihidroksivitamin D₃, (24R)-hidroksikalcidiol, 24(R),25-(OH)₂D₃)^[3] je jedinjenje koje je blisko srodno sa 1,25-dihidroksivitamin D₃, aktivnom formom vitamina D₃, ali je poput samog vitamina D₃ i 25-hidroksivitamina D₃ neaktivan kao hormon in vitro^[4] i in vivo.^[5]^[6]

Reference[уреди | уреди извор]

^ 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.
^ "Nomenclature of Vitamin D. Recommendations 1981. IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN) Архивирано на сајту Wayback Machine (23. август 2017)" reproduced at the Queen Mary, University of London website. Retrieved 21 March 2010.
^ Sørnes, S.; Bjøro, T.; Berg, J. P.; Torjesen, P. A.; Haug, E. (1994). „Calcitriol attenuates the basal and vasoactive intestinal peptide-stimulated cAMP production in prolactin-secreting rat pituitary (GH4C1) cells”. Molecular and cellular endocrinology. 101 (1–2): 183—188. PMID 9397951.
^ Mortensen, B. M.; Gautvik, K. M.; Gordeladze, J. O. (1993). „Bone turnover in rats treated with 1,25-dihydroxyvitamin D3, 25-hydroxyvitamin D3 or 24,25-dihydroxyvitamin D3”. Bioscience reports. 13 (1): 27—39. PMID 8392394.
^ Holick, MF; Schnoes, HK; Deluca, HF; Gray, RW; Boyle, IT; Suda, T (1972). „Isolation and identification of 24,25-dihydroxycholecalciferol, a metabolite of vitamin D made in the kidney”. Biochemistry. 11 (23): 4251—5. PMID 4342902. doi:10.1021/bi00773a009.

Literatura[уреди | уреди извор]

Mata-Granados, J. M.; Luque De Castro, M. D.; Quesada Gomez, J. M. (2008). „Inappropriate serum levels of retinol, α-tocopherol, 25 hydroxyvitamin D3 and 24,25 dihydroxyvitamin D3 levels in healthy Spanish adults: Simultaneous assessment by HPLC”. Clinical Biochemistry. 41: 676—680. PMID 18313404. doi:10.1016/j.clinbiochem.2008.02.003.

Spoljašnje veze[уреди | уреди извор]

[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] "Nomenclature of Vitamin D. Recommendations 1981. IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN) Архивирано на сајту Wayback Machine (23. август 2017)" reproduced at the Queen Mary, University of London website. Retrieved 21 March 2010.

[4] Sørnes, S.; Bjøro, T.; Berg, J. P.; Torjesen, P. A.; Haug, E. (1994). „Calcitriol attenuates the basal and vasoactive intestinal peptide-stimulated cAMP production in prolactin-secreting rat pituitary (GH4C1) cells”. Molecular and cellular endocrinology. 101 (1–2): 183—188. PMID 9397951.

[5] Mortensen, B. M.; Gautvik, K. M.; Gordeladze, J. O. (1993). „Bone turnover in rats treated with 1,25-dihydroxyvitamin D3, 25-hydroxyvitamin D3 or 24,25-dihydroxyvitamin D3”. Bioscience reports. 13 (1): 27—39. PMID 8392394.

[6] Holick, MF; Schnoes, HK; Deluca, HF; Gray, RW; Boyle, IT; Suda, T (1972). „Isolation and identification of 24,25-dihydroxycholecalciferol, a metabolite of vitamin D made in the kidney”. Biochemistry. 11 (23): 4251—5. PMID 4342902. doi:10.1021/bi00773a009.

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