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1 otubule depolymerizing drugs (colchicine and podophyllotoxin).
2 he important antiviral and anticancer agent, podophyllotoxin.
3 ymerization is retarded but not prevented by podophyllotoxin.
4 synthetic epimerization and demethylation of podophyllotoxin.
8 e of the potent antimitotic natural products podophyllotoxin and combretastatin A-4 and to that of NS
9 ve evolved in vascular plants; some, such as podophyllotoxin and enterodiol, have important roles in
10 first catalytic, asymmetric synthesis of (-)-podophyllotoxin and its C(2)-epimer, (-)-picropodophylli
17 Polygamain has structural similarities to podophyllotoxin, and molecular modeling simulations were
20 cation of enzymes putatively involved in (-)-podophyllotoxin biosynthesis and underscores the deducti
21 genes previously established as involved in podophyllotoxin biosynthesis as well as other candidate
22 ace similar to the trimethoxyphenyl group of podophyllotoxin but with distinct interactions within th
24 bited the binding of crocin to tubulin while podophyllotoxin did not inhibit the crocin binding indic
25 nacol (7beta-OH) series behaved similarly to podophyllotoxin in all the assays and proved to be the m
26 8-8'-lignans, including the antiviral agent podophyllotoxin in Podophyllum species and its semi-synt
27 (lactonization, SEM deprotection) or to (-)-podophyllotoxin, in three steps, through the introductio
28 GTP and taxol or DMSO, is very sensitive to podophyllotoxin inhibition, and can overcome urea-mediat
30 xol, colchicine, or other MBAs (vincristine, podophyllotoxin, nocodazole) stimulated the activity of
34 ran derivatives of alpha-conidendrin (ACON), podophyllotoxin (PT), and sikkimotoxin (SK) were prepare
36 y bullatacin and various antimitotic agents (podophyllotoxin, vinblastine, and colchicine), but only
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