An overview of tubulin inhibitors that interact with the colchicine binding site
Tubulin dynamics is a promising target for new chemotherapeutic agents. The colchicine
binding site is one of the most important pockets for potential tubulin polymerization …
binding site is one of the most important pockets for potential tubulin polymerization …
Tubulin inhibitors targeting the colchicine binding site: a perspective of privileged structures
The vital roles of microtubule in mitosis and cell division make it an attractive target for
antitumor therapy. Colchicine binding site of tubulin is one of the most important pockets that …
antitumor therapy. Colchicine binding site of tubulin is one of the most important pockets that …
From antibacterial to antitumour agents: a brief review on the chemical and medicinal aspects of sulfonamides
H Azevedo-Barbosa, DF Dias, LL Franco… - Mini Reviews in …, 2020 - ingentaconnect.com
Sulfonamides have been in clinical use for many years, and the development of bioactive
substances containing the sulfonamide subunit has grown steadily in view of their important …
substances containing the sulfonamide subunit has grown steadily in view of their important …
Development of combretastatins as potent tubulin polymerization inhibitors
The combretastatins are isolated from South African tree combretum caffrum kuntze. The
lead compound combretastatin A-4 has displayed remarkable cytotoxic effect in a wide …
lead compound combretastatin A-4 has displayed remarkable cytotoxic effect in a wide …
Styryl group, a friend or foe in medicinal chemistry
D Bhurta, SB Bharate - ChemMedChem, 2022 - Wiley Online Library
Abstract The styryl (Ph‐CH= CH‐R) group is widely represented in medicinally important
compounds, including drugs, clinical candidates, and molecular probes as it positively …
compounds, including drugs, clinical candidates, and molecular probes as it positively …
Phenylpropanoid-based sulfonamide promotes cyclin D1 and cyclin E down-regulation and induces cell cycle arrest at G1/S transition in estrogen positive MCF-7 cell …
H Azevedo-Barbosa, GÁ Ferreira-Silva, CF Silva… - Toxicology in Vitro, 2019 - Elsevier
Cancer is one of the most critical problems of public health in the world and one of the main
challenges for medicine. Different biological effects have been reported for sulfonamide …
challenges for medicine. Different biological effects have been reported for sulfonamide …
Photocatalytic Intramolecular Alkene Hydroamination of N-Alkoxy Ureas: An Approach to Imidazolinones
K Hu, YX He, ZY Lei, Y Ran, S Geng… - The Journal of …, 2023 - ACS Publications
Imidazolinones were obtained in good yields by intramolecular hydroamination of N-alkoxy
ureas in the presence of an organic photocatalyst and an inorganic base. In this reaction, the …
ureas in the presence of an organic photocatalyst and an inorganic base. In this reaction, the …
Antitubulin sulfonamides: The successful combination of an established drug class and a multifaceted target
A Vicente‐Blázquez, M González… - Medicinal research …, 2019 - Wiley Online Library
Tubulin, the microtubules and their dynamic behavior are amongst the most successful
antitumor, antifungal, antiparasitic, and herbicidal drug targets. Sulfonamides are exemplary …
antitumor, antifungal, antiparasitic, and herbicidal drug targets. Sulfonamides are exemplary …
Design, Synthesis, In Vitro Biological Activity Evaluation and Stabilized Nanostructured Lipid Carrier Formulation of Newly Synthesized Schiff Bases-Based TMP …
A series of novel Schiff bases-based TMP moieties have been designed and synthesized as
potential anticancer agents. The target Schiff bases were screened for their cytotoxic activity …
potential anticancer agents. The target Schiff bases were screened for their cytotoxic activity …
4-(3-Alkyl-2-oxoimidazolidin-1-yl)-N-phenylbenzenesulfonamide salts: Novel hydrosoluble prodrugs of antimitotics selectively bioactivated by the cytochrome P450 …
V Ouellette, ACC Alvarez, C Bouzriba… - Bioorganic …, 2023 - Elsevier
(3-Alkyl-2-oxoimidazolidin-1-yl)-N-phenylbenzenesulfonamides (PAIB-SAs) are members of
a new family of prodrugs bioactivated by cytochrome P450 1A1 (CYP1A1) in breast cancer …
a new family of prodrugs bioactivated by cytochrome P450 1A1 (CYP1A1) in breast cancer …