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VitaMin D4

VitaMin D4 ??? ???
?? ??:
511-28-4
???:
VitaMin D4
???(??):
VITAMIN D;COLECALCIFEROL;CALCIOL;RACUMIN D;Duphafral;Vtamin D4;vitamin D4;VITAMINE D4;OLEOVITAMIN D3;CHOLECALCIFEROLUM
CBNumber:
CB3104866
???:
C28H46O
??? ??:
398.66
MOL ??:
511-28-4.mol

VitaMin D4 ??

???
83-86 °C(lit.)
??
D18 +89.3° (c = 0.47 in acetone)
?? ?
504.9±29.0 °C(Predicted)
??
0.96
?? ??
2-8°C
???
?????? ???
??? ??
??
?? ?? (pKa)
14.74±0.20(Predicted)
??
Off-white to light yellow
???
???, ??? ???
InChIKey
DIPPFEXMRDPFBK-JPWDPSJFSA-N
SMILES
[C@H]1(O)CCC(=C)/C(=C\C=C2/CCC[C@@]3(C)[C@@]/2([H])CC[C@@H]3[C@H](C)CC[C@H](C)C(C)C)/C1
CAS ??????
511-28-4(CAS DataBase Reference)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? T+
?? ???? ?? 24/25-26-48/25
????? 28-36/37
????(UN No.) UN 2811 6.1/PG 2
WGK ?? 2
RTECS ?? VS2900000
F ?????? 8-10-23
???? ??? 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard Classifications Acute Tox. 2 Inhalation
Acute Tox. 3 Dermal
Acute Tox. 3 Oral
STOT RE 1 Oral
????(GHS): Skull and Crossbones (GHS06)Health Hazard (GHS08)
?? ?: Danger
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H330 ???? ???? ?? ?? ?? ?? ?? 1, 2 ?? P260, P271, P284, P304+P340, P310,P320, P403+P233, P405, P501
H372 ??? ?? ?? ???? ??(??, ??? ?? ??? ?? ??? ??)? ??? ??? ?? ???? ?? - ?? ?? ?? 1 ?? P260, P264, P270, P314, P501
??????:
P280 ????/???/???/?????? ?????.
P314 ???? ??? ???? ??·??? ????.
NFPA 704
0
4 0

VitaMin D4 C??? ??, ??, ??

??

Derived from cholesterol, vitamin D is biosynthesized from its prohormone cholecalciferol (D3), the product of solar ultraviolet irradiation of 7-dehydrocholesterol in the skin. In 1966, it was first recognized that vitamin D must undergo activation via two oxidative metabolic steps. The first oxidation to 25-hydroxycholecalciferol (25(OH)D3: calcifediol; Calderol) occurs in the endoplasmic reticulum of the liver and is catalyzed by vitamin D 25-hydroxylase. This activation step is not regulated by plasma calcium concentrations. The major circulating form (10–80 μg/mL) is 25(OH)D3, which also is the primary storage form of vitamin D.

??? ??

Pale Yellow Oil

??

Vitamin D4 is the active analogue of Vitamin D.

Biological Functions

Sterol-specific cytoplasmic receptor proteins (vitamin D receptor) mediate the biological action of vitamin D. The active hormone is transported from the cytoplasm to the nucleus via the vitamin D receptor, and as a result of the interaction of the hormone with target genes, a variety of proteins are produced that stimulate the transport of calcium in each of the target tissues Active vitamin D works in concert with PTH to enhance active intestinal absorption of calcium, to stimulate bone resorption, and to prohibit renal excretion of calcium. If serum calcium or 1,25-calcitriol concentrations are elevated, then vitamin D 24-hydroxylase (in renal mitochondria) is activated to oxidize 25(OH)D3 to inactive 24,25-dihydroxy-cholecalciferol and to further oxidize active vitamin D to the inactive 1,24,25-trihydroxylated derivative. Both the 1,24,25-trihydroxylated and the 24,25-dihydroxylated products have been found to suppress PT H secretion as well. The biosynthesis of vitamin D is tightly regulated based on the serum concentrations of calcium, phosphate, PTH, and active vitamin D.

Source

Vitamin D is a 9,10-secosteroid and 6 forms have been identified. The importance of vitamin D in bone (calcium homeostasis) is well established, and vitamin D has been the subject of increased attention in recent years for its role in muscle function, immunology, heart and cardiovascular disease, cancer, and insulin secretion. The vitamin D4 precursor 22,23-dihydroergosterol was present in all mushroom composites. The levels were not correlated with vitamin D4, but differed among species. Enoki mushrooms had a notably higher 22,23-dihydroergosterol content, with an average of 16.5 mg/100g compared to 4.49–8.89 mg/ 100 g in other types of mushrooms.

VitaMin D4 ?? ?? ? ???

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VitaMin D4 ?? ??

???( 208)?? ??
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VitaMin D4 ?? ??:

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