Synthesis and antiproliferative evaluation of glucosylated pyrazole analogs of K252c-Reference-Cited by-同舟云学术

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Synthesis and antiproliferative evaluation of glucosylated pyrazole analogs of K252c

Published:2018-02 Issue:8 Volume:74 Page:892-901
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Douara Bachir,Esvan Yannick J.,Pereira Elisabeth,Giraud Francis,Volodina Yulia L.,Kaluzhny Dmitry N.,Shtil Alexander A.,Anizon Fabrice,Moreau Pascale

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Biological Targets of Antitumor Indolocarbazoles Bearing a Sugar Moiety

2. A new alkaloid AM-2282 of Streptomyces origin taxonomy, fermentation, isolation and preliminary characterization.

3. A quantitative analysis of kinase inhibitor selectivity

4. https://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm555756.htm (accessed November 13, 2017).

5. Synthesis and biological activity of pyrazole analogues of the staurosporine aglycon K252c

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1. Synthesis, kinase inhibition and anti-leukemic activities of diversely substituted indolopyrazolocarbazoles;European Journal of Medicinal Chemistry;2024-04

2. Recent synthetic strategies for the construction of functionalized carbazoles and their heterocyclic motifs enabled by Lewis acids;RSC Advances;2023

3. Sequential Metal Catalysis towards 7‐Oxostaurosporine and Its Non‐Natural Septanose Analogue;Angewandte Chemie;2021-12

4. Sequential Metal Catalysis towards 7‐Oxostaurosporine and Its Non‐Natural Septanose Analogue;Angewandte Chemie International Edition;2021-11-30

5. Carbazole scaffolds in cancer therapy: a review from 2012 to 2018;Journal of Enzyme Inhibition and Medicinal Chemistry;2019-01-01

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