about
Crystal structure of 9-amino-N-[2-(4-morpholinyl)ethyl]-4-acridinecarboxamide bound to d(CGTACG)2: implications for structure-activity relationships of acridinecarboxamide topoisomerase poisons.Acridine Derivatives as Inhibitors of the IRE1α-XBP1 Pathway Are Cytotoxic to Human Multiple Myeloma.The dual topoisomerase inhibitor A35 preferentially and specially targets topoisomerase 2α by enhancing pre-strand and post-strand cleavage and inhibiting DNA religationGold(III) macrocycles: nucleotide-specific unconventional catalytic inhibitors of human topoisomerase I.Dual inhibition: a novel promising pharmacological approach for different disease conditions.
P2860
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
Dual topoisomerase I/II poisons as anticancer drugs.
@en
Dual topoisomerase I/II poisons as anticancer drugs.
@nl
type
label
Dual topoisomerase I/II poisons as anticancer drugs.
@en
Dual topoisomerase I/II poisons as anticancer drugs.
@nl
prefLabel
Dual topoisomerase I/II poisons as anticancer drugs.
@en
Dual topoisomerase I/II poisons as anticancer drugs.
@nl
P2860
P1476
Dual topoisomerase I/II poisons as anticancer drugs.
@en
P2093
P2860
P304
P356
10.1517/13543784.6.12.1845
P407
P577
1997-12-01T00:00:00Z