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1.
Modular and quasimodular solutions of a specific second order differential equation in the upper-half plane, which originates from a study of supersingular j-invariants in the first author's work with Don Zagier, are given explicitly. Positivity of Fourier coefficients of some of the solutions as well as a characterization of the differential equation are also discussed. 相似文献
2.
Sachiko Yamada Keiko Nakayama Hiroaki Takayama Toshimasa Shinki Tatsuo Suda 《Tetrahedron letters》1984,25(30):3239-3242
(25)-25,26-Dihydroxy-23-oxovitamin D3 was synthesized efficiently and stereoselectively, and it was converted enzymatically to (25)-1α,25,26-trihydroxy-23-oxovitamin D3, a putative metabolite of 1α,25-dihydroxyvitamin D3. The spectral and chemical properties of (25)-25,26-dihydroxy-23-oxovitamin D3 and its 1α,hydroxylated derivative disagree with those reported for the isolated metabolite. 相似文献
3.
The Pictet-Spengler reaction of tryptamine type 1,2-dihydropyridine 5c derived from the cycloaddition of the sec-nitrodienamine 3c with acetaldehyde afforded the indoloquinolizine derivatives 6 and 7. 相似文献
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H Miyazaki N Ohkawa N Nakamura T Ito T Sada T Oshima H Koike 《Chemical & pharmaceutical bulletin》1989,37(9):2379-2390
Six-membered lactone and tetrahydropyran analogues of platelet-activating factor (PAF), 4-11, and related antagonistic derivatives 41-46 were synthesized. None of the delta-lactones 4-7 showed PAF-like activities, while the corresponding cyclic ethers 8, 9 and 11 were slightly active. Some of the cyclic antagonists showed more potent inhibitory activities than the open chain antagonist CV-3988 against platelet aggregation (rabbit platelet-rich plasma, IC50) and hypotension (rat, ID50) induced by C16-PAF: e.g. dl-3-[6-[O-(trans-3-heptadecylcarbamoyloxytetrahydropyran-2- yl)methyl]phosphonoxy]hexylthiazolium (inner salt) (41d) (IC50 5.5 x 10(-7) M, ID50 0.046 mg/kg, i.v.); dl-3-[5-[O-(cis-3-heptadecylcarbamoylthiotetrahydropyran-2- yl)methyl]phosphonoxy]pentylthiazolium (inner salt) (43c) (IC50 5.7 x 10(-7) M, ID50 0.076 mg/kg, i.v.). 相似文献
10.
Tamura S Fukamiya N Okano M Koyama J Koike K Tokuda H Aoi W Takayasu J Kuchide M Nishino H 《Chemical & pharmaceutical bulletin》2003,51(4):385-389
Three new quassinoids, ailantinol E (1), ailantinol F (2), and ailantinol G (3), and related compounds were isolated from Ailanthus altissima grown in Taiwan. Their structures were elucidated from spectral evidence. Each new quassinoid was evaluated for its antitumor promoting effects against Epstein-Barr virus early antigen activation introduced by 12-O-tetradecanoylphorbol-13-acetate in Raji cells. The new quassinoids were found to show potent activity without showing any cytotoxicity. The screening for inhibitors against nitric oxide donor action was also conducted using the new quassinoids and some standard samples. 相似文献