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1 otubule depolymerizing drugs (colchicine and podophyllotoxin).
2 the disassembly-inducing reagents Ca(2+) and podophyllotoxin.
3 he important antiviral and anticancer agent, podophyllotoxin.
4 ymerization is retarded but not prevented by podophyllotoxin.
5 dihydroindenolactone compound instead of (-)-podophyllotoxin.
6 synthetic epimerization and demethylation of podophyllotoxin.
7 immediate precursor of etoposide and, unlike podophyllotoxin, a potent topoisomerase inhibitor.
8       Podophyllum species are sources of (-)-podophyllotoxin, an aryltetralin lignan used for semi-sy
9                                 In addition, podophyllotoxin and CA-4 inhibited the binding of compou
10 e of the potent antimitotic natural products podophyllotoxin and combretastatin A-4 and to that of NS
11 ve evolved in vascular plants; some, such as podophyllotoxin and enterodiol, have important roles in
12 first catalytic, asymmetric synthesis of (-)-podophyllotoxin and its C(2)-epimer, (-)-picropodophylli
13                                              Podophyllotoxin and nocodazole, other colchicine site li
14  short chemoenzymatic total synthesis of (-)-podophyllotoxin and related aryltetralin lignans.
15 stereo and chemoselective transformations of podophyllotoxin and several amino alcohols.
16 38067 and the noncovalent agents colchicine, podophyllotoxin, and 2-methoxyestradiol.
17 ent antimitotic natural products colchicine, podophyllotoxin, and combretastatin A-4.
18 g effects comparable to those of colchicine, podophyllotoxin, and combretastatin A-4.
19 ent antimitotic natural products colchicine, podophyllotoxin, and combretastatin A-4.
20 ent antimitotic natural products colchicine, podophyllotoxin, and combretastatin A-4.
21 molecules such as stanozolol, (-)-ambroxide, podophyllotoxin, and dideoxyribose.
22    Polygamain has structural similarities to podophyllotoxin, and molecular modeling simulations were
23            Derivatives of alpha-conidendrin, podophyllotoxin, and sikkimotoxin were prepared to evalu
24               Several pinacol derivatives of podophyllotoxins bearing different side chains and funct
25 cation of enzymes putatively involved in (-)-podophyllotoxin biosynthesis and underscores the deducti
26  genes previously established as involved in podophyllotoxin biosynthesis as well as other candidate
27 ace similar to the trimethoxyphenyl group of podophyllotoxin but with distinct interactions within th
28                                      A novel podophyllotoxin derivative, XWL-1-48, was synthesized as
29 bited the binding of crocin to tubulin while podophyllotoxin did not inhibit the crocin binding indic
30         Our study used a ternary phycocyanin-podophyllotoxin-IDO1 self-assembled nanoplatform to inve
31 nacol (7beta-OH) series behaved similarly to podophyllotoxin in all the assays and proved to be the m
32  8-8'-lignans, including the antiviral agent podophyllotoxin in Podophyllum species and its semi-synt
33  (lactonization, SEM deprotection) or to (-)-podophyllotoxin, in three steps, through the introductio
34  GTP and taxol or DMSO, is very sensitive to podophyllotoxin inhibition, and can overcome urea-mediat
35                                          (-)-Podophyllotoxin is one of the most potent microtubule de
36                                              Podophyllotoxin is the natural product precursor of the
37 xol, colchicine, or other MBAs (vincristine, podophyllotoxin, nocodazole) stimulated the activity of
38 bited by the antimicrotubule drugs Colcemid, podophyllotoxin, nocodazole, and vinblastine.
39 bioactive small molecules including AZD6244, podophyllotoxin, paclitaxel, and docetaxel.
40 apple) to identify biosynthetic genes in the podophyllotoxin pathway.
41 ran derivatives of alpha-conidendrin (ACON), podophyllotoxin (PT), and sikkimotoxin (SK) were prepare
42                   A short total synthesis of podophyllotoxin, the prototypical aryltetralin lignan na
43 y bullatacin and various antimitotic agents (podophyllotoxin, vinblastine, and colchicine), but only