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Fighting tumor cell survival: advances in the design and evaluation of Pim inhibitors

Current medicinal chemistry, 2010-12, Vol.17 (34), p.4114-4133

2010

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Synthesis of granulatimide bis-imide analogues

Tetrahedron, 2005-06, Vol.61 (23), p.5599-5614

2005

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Synthesis and antiproliferative activities of diversely substituted glycosyl-isoindigo derivatives

European journal of medicinal chemistry, 2006, Vol.41 (1), p.88-100

2006

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Synthesis of glycosyl-isoindigo derivatives

Tetrahedron letters, 2004-06, Vol.45 (25), p.4827-4830

2004

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Synthesis of bridged aza-rebeccamycin analogues

Tetrahedron, 2005-07, Vol.61 (30), p.7304-7316

2005

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Synthesis of dipyrrolo[3,4- a:3,4- c]carbazole-1,3,4,6-tetraones bearing a sugar moiety

Tetrahedron, 2006-02, Vol.62 (6), p.1116-1123

2006

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Synthesis of pyridino[3′,2′:4,5]pyrrolo[3,2- g]pyrrolo[3,4- e]indolizin-1,3-dione and pyrrolo[3,2- c]pyrazole skeletons

Tetrahedron letters, 2006-01, Vol.47 (4), p.433-436

2006

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Synthesis of a staurosporine analogue possessing a 7-azaindole unit instead of an indole moiety

Tetrahedron letters, 2004-06, Vol.45 (24), p.4643-4647

2004

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Synthesis and cytotoxicities of 7-aza rebeccamycin analogues bearing various substituents on the sugar moiety, on the imide nitrogen and on the carbazole framework

European journal of medicinal chemistry, 2005-10, Vol.40 (10), p.961-971

2005

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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

Molecular pharmacology, 1999-02, Vol.55 (2), p.377-385

1999

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Rebeccamycin analogues bearing amine substituents or other groups on the sugar moiety

Bioorganic & medicinal chemistry, 2003-08, Vol.11 (17), p.3709-3722

2003

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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

Journal of medicinal chemistry, 1997-10, Vol.40 (21), p.3456-3465

1997

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Syntheses and Antiproliferative Activities of New Rebeccamycin Derivatives with the Sugar Unit Linked to Both Indole Nitrogens

Journal of medicinal chemistry, 2002-03, Vol.45 (6), p.1330-1339

2002

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Semi-synthesis, topoisomerase I and kinases inhibitory properties, and antiproliferative activities of new rebeccamycin derivatives

Bioorganic & medicinal chemistry, 2003-11, Vol.11 (23), p.4871-4879

2003

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Bicyclic 6-6 Systems: Other Four Heteroatoms 2/2

Reference Module in Chemistry, Molecular Sciences and Chemical Engineering, 2013

2013

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Syntheses and Biological Activities of Rebeccamycin Analogues. Introduction of a Halogenoacetyl Substituent

Journal of medicinal chemistry, 1999-02, Vol.42 (4), p.584-592

1999

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Syntheses and Biological Evaluation of Indolocarbazoles, Analogues of Rebeccamycin, Modified at the Imide Heterocycle

Journal of medicinal chemistry, 1998-05, Vol.41 (10), p.1631-1640

1998

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DNA targeting of two new antitumour rebeccamycin derivatives

European journal of medicinal chemistry, 2002-12, Vol.37 (12), p.925-932

2002

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Formaldehyde-Induced Alkylation of a 2‘-Aminoglucose Rebeccamycin Derivative to Both A·T and G·C Base Pairs in DNA

Journal of medicinal chemistry, 2000-11, Vol.43 (24), p.4711-4720

2000

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Synthesis, Mode of Action, and Biological Activities of Rebeccamycin Bromo Derivatives

Journal of medicinal chemistry, 1999-05, Vol.42 (10), p.1816-1822

1999

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Syntheses, biochemical and biological evaluation of staurosporine analogues from the microbial metabolite rebeccamycin

Bioorganic & medicinal chemistry, 1998-09, Vol.6 (9), p.1597-1604

1998

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Synthesis and Characterisation of a Doxorubicin-CNGRC Peptide Conjugate that Targets Tumour Vasculature

Synthesis (Stuttgart), 2002, Vol.2002 (18), p.2733-2736

2002

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Formaldehyde-Induced Alkylation of a 2'-Aminoglucose Rebeccamycin Derivative to Both A times T and G times C Base Pairs in DNA

Journal of medicinal chemistry, 2000-11, Vol.43 (24), p.4711-4720

2000

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Formaldehyde-induced alkylation of a 2'-aminoglucose rebeccamycin derivative to both A.T and G.C base pairs in DNA

Journal of medicinal chemistry, 2000-11, Vol.43 (24), p.4711-4720

2000

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Cellular uptake and interaction with purified membranes of rebeccamycin derivatives

European journal of pharmacology, 2000-02, Vol.389 (2), p.141-146

2000

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Fighting tumor cell survival: advances in the design and evaluation of Pim inhibitors

Synthesis of granulatimide bis-imide analogues

Synthesis and antiproliferative activities of diversely substituted glycosyl-isoindigo derivatives

Synthesis of glycosyl-isoindigo derivatives

Synthesis of bridged aza-rebeccamycin analogues

Synthesis of dipyrrolo[3,4- a:3,4- c]carbazole-1,3,4,6-tetraones bearing a sugar moiety

Synthesis of pyridino[3′,2′:4,5]pyrrolo[3,2- g]pyrrolo[3,4- e]indolizin-1,3-dione and pyrrolo[3,2- c]pyrazole skeletons

Synthesis of a staurosporine analogue possessing a 7-azaindole unit instead of an indole moiety

Synthesis and cytotoxicities of 7-aza rebeccamycin analogues bearing various substituents on the sugar moiety, on the imide nitrogen and on the carbazole framework

Enhanced Binding to DNA and Topoisomerase I Inhibition by an Analog of the Antitumor Antibiotic Rebeccamycin Containing an Amino Sugar Residue

Rebeccamycin analogues bearing amine substituents or other groups on the sugar moiety

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

Syntheses and Antiproliferative Activities of New Rebeccamycin Derivatives with the Sugar Unit Linked to Both Indole Nitrogens

Semi-synthesis, topoisomerase I and kinases inhibitory properties, and antiproliferative activities of new rebeccamycin derivatives

Bicyclic 6-6 Systems: Other Four Heteroatoms 2/2

Syntheses and Biological Activities of Rebeccamycin Analogues. Introduction of a Halogenoacetyl Substituent

Syntheses and Biological Evaluation of Indolocarbazoles, Analogues of Rebeccamycin, Modified at the Imide Heterocycle

DNA targeting of two new antitumour rebeccamycin derivatives

Formaldehyde-Induced Alkylation of a 2‘-Aminoglucose Rebeccamycin Derivative to Both A·T and G·C Base Pairs in DNA

Synthesis, Mode of Action, and Biological Activities of Rebeccamycin Bromo Derivatives

Syntheses, biochemical and biological evaluation of staurosporine analogues from the microbial metabolite rebeccamycin

Synthesis and Characterisation of a Doxorubicin-CNGRC Peptide Conjugate that Targets Tumour Vasculature

Formaldehyde-Induced Alkylation of a 2'-Aminoglucose Rebeccamycin Derivative to Both A times T and G times C Base Pairs in DNA

Formaldehyde-induced alkylation of a 2'-aminoglucose rebeccamycin derivative to both A.T and G.C base pairs in DNA

Cellular uptake and interaction with purified membranes of rebeccamycin derivatives

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