- 日
- 関
- 同
- Calciferol, Drisdol
- 同
- vitamin D2
- 同
- Calciferol, Drisdol
- 同
- vitamin D2
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/05/07 12:10:46」(JST)
[Wiki en表示]
"Calcidol" redirects here. For the form of vitamin D3 sometimes called "calcidiol", see Cholecalciferol.
Ergocalciferol |
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IUPAC name
(3β,5Z,7E,22E)-9,10-secoergosta-5,7,10(19),22-tetraen-3-ol
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Other names
Drisdol (Sanofi-Synthelabo), Calcidol (Patrin Pharma)
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Identifiers |
CAS number |
50-14-6 Y |
PubChem |
5280793 |
ChemSpider |
4444351 Y |
UNII |
VS041H42XC Y |
DrugBank |
DB00153 |
KEGG |
C05441 Y |
ChEBI |
CHEBI:28934 Y |
ChEMBL |
CHEMBL1536 Y |
ATC code |
A11CC01 |
Jmol-3D images |
Image 1 |
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O[C@@H]1CC(\C(=C)CC1)=C\C=C2/CCC[C@]3([C@H]2CC[C@@H]3[C@@H](/C=C/[C@H](C)C(C)C)C)C
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InChI=1S/C28H44O/c1-19(2)20(3)9-10-22(5)26-15-16-27-23(8-7-17-28(26,27)6)12-13-24-18-25(29)14-11-21(24)4/h9-10,12-13,19-20,22,25-27,29H,4,7-8,11,14-18H2,1-3,5-6H3/b10-9+,23-12+,24-13-/t20-,22+,25-,26+,27-,28+/m0/s1 Y
Key: MECHNRXZTMCUDQ-RKHKHRCZSA-N Y
InChI=1/C28H44O/c1-19(2)20(3)9-10-22(5)26-15-16-27-23(8-7-17-28(26,27)6)12-13-24-18-25(29)14-11-21(24)4/h9-10,12-13,19-20,22,25-27,29H,4,7-8,11,14-18H2,1-3,5-6H3/b10-9+,23-12+,24-13-/t20-,22+,25-,26+,27-,28+/m0/s1
Key: MECHNRXZTMCUDQ-RKHKHRCZBW
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Properties |
Molecular formula |
C28H44O |
Molar mass |
396.65 g/mol |
Melting point |
114–118 °C
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Y (verify) (what is: Y/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
Infobox references |
Ergocalciferol is a provitamin form of vitamin D, also called vitamin D2. In isolated manufactured formats, it is marketed under various names including Deltalin (Eli Lilly and Company), discontinued Drisdol (Sanofi-Synthelabo), and Calcidol (Patrin Pharma). Ergocalciferol is created when ultraviolet light activates ergosterol.[citation needed]
Ergocalciferol may be used as a vitamin D supplement, and a 2011 clinical guideline[1] considered it to be as effective as cholecalciferol (vitamin D3), which is produced naturally by the skin when exposed to ultraviolet light. Conflicting evidence exists for how similarly D2 and D3 behave in the body and whether they are equally active, with preliminary studies suggesting D3 is more potent,[2][3] while others report equal efficacy.[1][4][5] Cholecalciferol (vitamin D3) is sensitive to UV radiation and rapidly, but reversibly, forms other sterols which can further irreversibly convert to ergosterol.[citation needed]
Contents
- 1 Sources
- 2 Preliminary research
- 3 References
- 4 External links
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Sources [edit]
Lichen
- Cladina arbuscula specimens grown under different natural conditions: The contents of vitamin D3 range from 0.67 to 2.04 μg/g dry matter in the thalli of C. arbuscula specimens grown under different natural conditions, while provitamin D3 could not be detected. The ranges for provitamin D2 and vitamin D2 were 89-146 and 0.22-0.55 μg/g dry matter, respectively, while the contents of provitamin D3 were below the detection limit (0.01 μg/g dry matter).[6]
Fungus, from USDA nutrient database[7]
- Mushrooms, portabella, exposed to ultraviolet light, raw: Vitamin D (D2 + D3): 11.2 mcg (446 IU)
- Mushrooms, portabella, exposed to ultraviolet light, grilled: Vitamin D (D2 + D3): 13.1 mcg (524 IU)
- Mushrooms, shiitake, dried: Vitamin D (D2 + D3): 3.9 μg (154 IU)
- Mushrooms, shiitake, raw: Vitamin D (D2 + D3): 0.4 μg (18 IU)
- Mushrooms, portabella, raw: Vitamin D (D2 + D3): 0.3 μg (10 IU)
Plantae
- Alfalfa (Medicago sativa subsp. sativa), shoot: 4.8 μg (192 IU) vitamin D2, 0.1 μg (4 IU) vitamin D3[8]
Ergocalciferol is produced in fungi synthetically through irradiation of ergosterol.[9] Human bioavailability of vitamin D2 from vitamin D2-enhanced button mushrooms via UV-B irradiation is effective in improving vitamin D status and not different to a vitamin D2 supplement.[10] Vitamin D2 from UV-irradiated yeast baked into bread is bioavailable.[11] By visual assessment or using a chromometer, no significant discoloration of irradiated mushrooms, as measured by the degree of "whiteness", was observed.[12] Claims have been made that a normal serving (approx. 3 oz or 1/2 cup, or 60 grams) of mushrooms treated with ultraviolet light provides vitamin D content to levels of 3,476 IU if exposed to just 5 minutes of UV light after being harvested.[13]
Preliminary research [edit]
One study found low vitamin D2 levels in patients with Alzheimer's disease,[14] but this observational study did not prove cause or effect related to ergocalciferol and vitamin D2 deficiency in the diet.
References [edit]
- ^ a b Holick, M. F.; Binkley, N. C.; Bischoff-Ferrari, H. A.; Gordon, C. M.; Hanley, D. A.; Heaney, R. P.; Murad, M. H.; Weaver, C. M. (2011). "Evaluation, Treatment, and Prevention of Vitamin D Deficiency: An Endocrine Society Clinical Practice Guideline". Journal of Clinical Endocrinology & Metabolism 96 (7): 1911. doi:10.1210/jc.2011-0385. PMID 21646368. edit
- ^ Houghton, L.; Vieth, R. (2006). "The case against ergocalciferol (vitamin D2) as a vitamin supplement". The American Journal of Clinical Nutrition 84 (4): 694–697. PMID 17023693. edit
- ^ Trang, H. M.; Cole, D. E.; Rubin, L. A.; Pierratos, A.; Siu, S.; Vieth, R. (1998). "Evidence that vitamin D3 increases serum 25-hydroxyvitamin D more efficiently than does vitamin D2". The American journal of clinical nutrition 68 (4): 854–858. PMID 9771862. edit
- ^ Holick Mf, B. R.; Biancuzzo, R. M.; Chen, T. C.; Klein, E. K.; Young, A.; Bibuld, D.; Reitz, R.; Salameh, W. et al. (2007). "Vitamin D2 is as Effective as Vitamin D3 in Maintaining Circulating Concentrations of 25-Hydroxyvitamin D". Journal of Clinical Endocrinology & Metabolism 93 (3): 677–681. doi:10.1210/jc.2007-2308. PMC 2266966. PMID 18089691. edit
- ^ Biancuzzo, R. M.; Young, A.; Bibuld, D.; Cai, M. H.; Winter, M. R.; Klein, E. K.; Ameri, A.; Reitz, R. et al. (2010). "Fortification of orange juice with vitamin D2 or vitamin D3 is as effective as an oral supplement in maintaining vitamin D status in adults". American Journal of Clinical Nutrition 91 (6): 1621–1626. doi:10.3945/ajcn.2009.27972. PMC 2869510. PMID 20427729. edit
- ^ Wang, T; Bengtsson, G; Kärnefelt, I; Björn, LO (2001). "Provitamins and vitamins D₂and D₃in Cladina spp. Over a latitudinal gradient: Possible correlation with UV levels". Journal of photochemistry and photobiology. B, Biology 62 (1–2): 118–22. PMID 11693362.
- ^ "USDA nutrient database – use the keyword 'portabella' and then click submit".
- ^ "Dr. Duke's Phytochemical and Ethnobotanical Databases".
- ^ "Vitamin D: A Rapid Review: Vitamin D2 and/or Vitamin D3". Medscape.com. 2008-06-30. Retrieved 2012-08-29.
- ^ http://www.nature.com/ejcn/journal/v65/n8/full/ejcn201153a.html
- ^ Hohman, E. E.; Martin, B. R.; Lachcik, P. J.; Gordon, D. T.; Fleet, J. C.; Weaver, C. M. (2011). "Bioavailability and Efficacy of Vitamin D2from UV-Irradiated Yeast in Growing, Vitamin D-Deficient Rats". Journal of Agricultural and Food Chemistry 59 (6): 2341–2346. doi:10.1021/jf104679c. PMC 3235799. PMID 21332187. edit
- ^ Koyyalamudi, SR; Jeong, SC; Song, CH; Cho, KY; Pang, G (2009). "Vitamin D2 formation and bioavailability from Agaricus bisporus button mushrooms treated with ultraviolet irradiation". J Agric Food Chem 57 (8): 3351–5. doi:10.1021/jf803908q. PMID 19281276.
- ^ "Bringing Mushrooms Out of the Dark". MSNBC. April 18, 2006. Retrieved 2007-08-06.
- ^ Iltaf Shah; Petroczi, Andrea; Tabet, Naji; Klugman, Anthony; Isaac, Mokhtar; p. Naughton, Declan (2012). "Low 25OH Vitamin D2 Levels Found in Untreated Alzheimer's Patients, Compared to Acetylcholinesterase-Inhibitor Treated and Controls". Current Alzheimer Research 9 (9): 1069–1076. doi:10.2174/156720512803568975. ISSN 1567-2050. PMID 22876849
External links [edit]
- NIST Chemistry WebBook page for ergocalciferol
Vitamins (A11)
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Fat soluble |
A
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α-Carotene · β-Carotene · Retinol# · Tretinoin
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D
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D2 (Ergosterol, Ergocalciferol#) · D3 (7-Dehydrocholesterol, Previtamin D3, Cholecalciferol, 25-hydroxycholecalciferol, Calcitriol (1,25-dihydroxycholecalciferol), Calcitroic acid) · D4 (Dihydroergocalciferol) · D5 · D analogues (Alfacalcidol, Dihydrotachysterol, Calcipotriol, Tacalcitol, Paricalcitol)
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E
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Tocopherol (Alpha, Beta, Gamma, Delta) · Tocotrienol (Alpha, Beta, Gamma, Delta) · Tocofersolan
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K
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Naphthoquinone · Phylloquinone (K1) · Menaquinones (K2) · Menadione (K3)‡ · Menadiol (K4)
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Water soluble |
B
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B1 (Thiamine#) · B2 (Riboflavin#) · B3 (Niacin, Nicotinamide#) · B5 (Pantothenic acid, Dexpanthenol, Pantethine) · B6 (Pyridoxine#, Pyridoxal phosphate, Pyridoxamine) · B7 (Biotin) · B9 (Folic acid, Dihydrofolic acid, Folinic acid, L-methylfolate) · B12 (Cyanocobalamin, Hydroxocobalamin, Methylcobalamin, Cobamamide) · Choline
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C
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Ascorbic acid# · Dehydroascorbic acid
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Combinations |
Multivitamins
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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noco, nuvi, sysi/epon, met
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Cholestanes, membrane lipids: sterols
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- Adosterol
- Cholecalciferol/Ergocalciferols
- Cholesterol
- Dihydrotachysterol
- Fusidic acid
- Lanosterol
- Phytosterols
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UpToDate Contents
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English Journal
- Effect of cholecalciferol recommended daily allowances on vitamin D status and fibroblast growth factor-23: An observational study in acute burn patients.
- Rousseau AF1, Damas P2, Ledoux D2, Cavalier E3.
- Burns : journal of the International Society for Burn Injuries.Burns.2014 Aug;40(5):865-70. doi: 10.1016/j.burns.2013.11.015. Epub 2014 Jan 23.
- OBJECTIVE: Burn patients are at risk of hypovitaminosis D. Optimal vitamin D (VD) intakes are not defined in burn nutrition guidelines and studies mostly focused on ergocalciferol (VD2) supplementation in burn children. Aim of our study was to describe adult burns VD status, to measure effects of ou
- PMID 24462294
- Vitamin D supplementation for prevention of cancer in adults.
- Bjelakovic G1, Gluud LL, Nikolova D, Whitfield K, Krstic G, Wetterslev J, Gluud C.
- The Cochrane database of systematic reviews.Cochrane Database Syst Rev.2014 Jun 23;6:CD007469. [Epub ahead of print]
- BACKGROUND: The evidence on whether vitamin D supplementation is effective in decreasing cancers is contradictory.OBJECTIVES: To assess the beneficial and harmful effects of vitamin D supplementation for prevention of cancer in adults.SEARCH METHODS: We searched the Cochrane Central Register of Cont
- PMID 24953955
- Vitamin D3, D2 and Arterial Wall Properties in Coronary Artery Disease.
- Siasos G, Tousoulis D, Oikonomou E, Maniatis K, Kioufis S, Kokkou E, Zaromitidou M, Kassi E, Miliou A, Stefanadis C1.
- Current pharmaceutical design.Curr Pharm Des.2014 Jun 19. [Epub ahead of print]
- Objectives: There are two major forms of vitamin D, vitamin D2 (ergocalciferol) and vitamin D3 (cholecalciferol). We studied the effect of the different vitamin D fractions (D3/D2) on arterial wall properties in coronary artery disease (CAD) patients. Methods: We included 252 subjects with CAD. Endo
- PMID 24947585
Japanese Journal
- Differences in outcomes between cholecalciferol and ergocalciferol supplementation in veterans with inflammatory bowel disease
- Geriatrics & gerontology international 12(3), 475-480, 2012-07-01
- NAID 10030991693
- Selective Inhibition of Mammalian DNA Polymerase α by Vitamin D_2 and D_3
Related Links
- The latest Tweets from かるしふぇ~ (@ergocalciferol). 金のごまどれ国民・超電磁砲・アニメ・ボカロ・息抜き・IAIA団. にほん ... 今ね、新SNS「tsu」というのに絶賛はまってます。やみつきになる人続出です。完全招待制のSNSなので登録は ...
- ergocalciferol /er·go·cal·cif·er·ol/ (er″go-kal-sif´er-ol) vitamin D; a sterol occurring in fungi and some fish oils or synthesized from ergosterol, with similar activity and metabolism to those of cholecalciferol; used as a dietary source of vitamin D ...
★リンクテーブル★
[★]
- 英
- calciferol
- 関
- エルゴカルシフェロール、ビタミンD2
- 関
- ergocalciferol、vitamin D2
ビタミンD
[★]
- 英
- ergocalciferol
- 同
- ビタミンD2 vitamin D2
- 関
- [[]]
[★]
25-ヒドロキシエルゴカルシフェロール
- 関
- 25-hydroxyvitamin D2