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Rebeccamycin analogues as anti-cancer agents
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12620658
retrieved
6 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Rebeccamycin analogues as anti-cancer agents
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12620658
retrieved
6 August 2017
author name string
Michelle Prudhomme
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12620658
retrieved
6 August 2017
publication date
1 February 2003
1 reference
stated in
Europe PubMed Central
PubMed ID
12620658
retrieved
6 August 2017
published in
European Journal of Medicinal Chemistry
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stated in
Europe PubMed Central
PubMed ID
12620658
retrieved
6 August 2017
volume
38
1 reference
stated in
Europe PubMed Central
PubMed ID
12620658
retrieved
6 August 2017
page(s)
123-140
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stated in
Europe PubMed Central
PubMed ID
12620658
retrieved
6 August 2017
issue
2
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stated in
Europe PubMed Central
PubMed ID
12620658
retrieved
6 August 2017
cites work
Production and biological activity of rebeccamycin, a novel antitumor agent.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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inferred from DOI database lookup
Isolation and structure of rebeccamycin - a new antitumor antibiotic from nocardia aerocoligenes
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reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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inferred from DOI database lookup
Discovery of antitumor indolocarbazoles: rebeccamycin, NSC 655649, and fluoroindolocarbazoles
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Synthesis of Rebeccamycin and 11-Dechlororebeccamycin
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reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Water soluble derivatives of rebeccamycin
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Syntheses and biological activities (topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group.
1 reference
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Recent developments of rebeccamycin analogues as topoisomerase I inhibitors and antitumor agents
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reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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DNA cleavage by topoisomerase I in the presence of indolocarbazole derivatives of rebeccamycin
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reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Recognition of specific sequences in DNA by a topoisomerase I inhibitor derived from the antitumor drug rebeccamycin
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reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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A new antitumor substance, BE-13793C, produced by a streptomycete. Taxonomy, fermentation, isolation, structure determination and biological activity
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Crossref
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Indolocarbazole poisons of human topoisomerase I: regioisomeric analogues of ED-110
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Synthesis and biological activities of NB-506 analogues modified at the glucose group
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reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Enhanced binding to DNA and topoisomerase I inhibition by an analog of the antitumor antibiotic rebeccamycin containing an amino sugar residue
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Formaldehyde-induced alkylation of a 2'-aminoglucose rebeccamycin derivative to both A.T and G.C base pairs in DNA.
1 reference
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent
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reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Binding of two novel bisdaunorubicins to DNA studied by NMR spectroscopy
1 reference
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Crossref
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7 January 2021
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Sequence-selective intercalation of antitumour bis-naphthalimides into DNA. Evidence for an approach via the major groove.
1 reference
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Dimers from dechlorinated rebeccamycin: synthesis, interaction with DNA, and antiproliferative activities.
1 reference
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Syntheses, biochemical and biological evaluation of staurosporine analogues from the microbial metabolite rebeccamycin
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Syntheses and antiproliferative activities of new rebeccamycin derivatives with the sugar unit linked to both indole nitrogens
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Rebeccamycin analogues from indolo[2,3-c]carbazole
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Crossref
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Syntheses and antiproliferative activities of rebeccamycin analogues bearing two 7-azaindole moieties
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Syntheses and antiproliferative activities of 7-azarebeccamycin analogues bearing one 7-azaindole moiety
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Crossref
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https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Cellular uptake and interaction with purified membranes of rebeccamycin derivatives.
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reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
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Recognition and cleavage of DNA by rebeccamycin- or benzopyridoquinoxaline conjugated of triple helix-forming oligonucleotides
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
based on heuristic
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Triple helix-forming oligonucleotides conjugated to indolocarbazole poisons direct topoisomerase I-mediated DNA cleavage to a specific site.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
based on heuristic
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Design of new anti-cancer agents based on topoisomerase poisons targeted to specific DNA sequences
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0223-5234%2803%2900011-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0223-5234(03)00011-4
1 reference
stated in
Europe PubMed Central
PubMed ID
12620658
retrieved
6 August 2017
PubMed ID
12620658
1 reference
stated in
Europe PubMed Central
PubMed ID
12620658
retrieved
6 August 2017
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