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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.
5 immediate precursor of etoposide and, unlike podophyllotoxin, a potent topoisomerase inhibitor.
6       Podophyllum species are sources of (-)-podophyllotoxin, an aryltetralin lignan used for semi-sy
7                                 In addition, podophyllotoxin and CA-4 inhibited the binding of compou
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
11                                              Podophyllotoxin and nocodazole, other colchicine site li
12 38067 and the noncovalent agents colchicine, podophyllotoxin, and 2-methoxyestradiol.
13 ent antimitotic natural products colchicine, podophyllotoxin, and combretastatin A-4.
14 g effects comparable to those of colchicine, podophyllotoxin, and combretastatin A-4.
15 ent antimitotic natural products colchicine, podophyllotoxin, and combretastatin A-4.
16 ent antimitotic natural products colchicine, podophyllotoxin, and combretastatin A-4.
17    Polygamain has structural similarities to podophyllotoxin, and molecular modeling simulations were
18            Derivatives of alpha-conidendrin, podophyllotoxin, and sikkimotoxin were prepared to evalu
19               Several pinacol derivatives of podophyllotoxins bearing different side chains and funct
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
23                                      A novel podophyllotoxin derivative, XWL-1-48, was synthesized as
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
29                                              Podophyllotoxin is the natural product precursor of the
30 xol, colchicine, or other MBAs (vincristine, podophyllotoxin, nocodazole) stimulated the activity of
31 bited by the antimicrotubule drugs Colcemid, podophyllotoxin, nocodazole, and vinblastine.
32 bioactive small molecules including AZD6244, podophyllotoxin, paclitaxel, and docetaxel.
33 apple) to identify biosynthetic genes in the podophyllotoxin pathway.
34 ran derivatives of alpha-conidendrin (ACON), podophyllotoxin (PT), and sikkimotoxin (SK) were prepare
35                   A short total synthesis of podophyllotoxin, the prototypical aryltetralin lignan na
36 y bullatacin and various antimitotic agents (podophyllotoxin, vinblastine, and colchicine), but only

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