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1  used to construct the dienyne precursors of previtamin 6 possessing two methyl groups capable of par
2 nalyzed in depth, i.e., the conformations of previtamin D and the quantum effects associated with the
3 e characterization of the conformers of both previtamin D and vitamin D allowed the calculation of th
4 analogue 12 was prone to conversion into its previtamin D form by thermal equilibration, the correspo
5 or-1alpha,25-(OH)2D3, were obtained from the previtamin D precursors, constructed by either Suzuki-Mi
6         Of the large number of conformers of previtamin D that were located, there are 16 that have t
7 he thermal isomerization reaction converting previtamin D to vitamin D is an intramolecular [1,7]-sig
8 to-isomers lumisterol(2), tachysterol(2) and previtamin D(2) increased in this order.
9 ) was the most abundant product, followed by previtamin D(2), lumisterol(2) and tachysterol(2) in ord
10  study, the ergosterol-derived photoproducts previtamin D(2), lumisterol(2) and tachysterol(2) were,
11 tly between groups nor did its conversion to previtamin D(3) after irradiation in vitro.
12 ntroduced by the flexibility of the rings of previtamin D.
13      We reported previously that the rate of previtamin D3 (preD3) <==> vitamin D3 isomerization was
14 at the conversion of 7-dehydrocholesterol to previtamin D3 was reduced in children a mean of 14 month
15 n the skin, leading to its transformation to previtamin D3, which is rapidly converted to vitamin D3.
16 sterification of the 3beta-hydroxy of preD3 (previtamin D3-3beta-acetate) reduced the rate of the iso
17  nm to determine their efficiency to produce previtamin D3.

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