Design, synthesis and anticancer studies of novel aminobenzazolyl pyrimidines as tyrosine kinase inhibitors

R Chikhale, S Thorat, RK Choudhary, N Gadewal… - Bioorganic …, 2018 - Elsevier
Abnormal signalling from the Protein tyrosine kinases (PTKs) like receptor tyrosine kinases
and intracellular tyrosine kinases can lead to diseases such as cancer especially non-small …

Benzothiazoles: Search for anticancer agents

MN Noolvi, HM Patel, M Kaur - European journal of medicinal chemistry, 2012 - Elsevier
Novel derivatives of 2-amino benzothiazoles 4 (a–j) have been synthesized and tested for
their antitumor activity using National Cancer Institute (NCI) disease oriented antitumor …

Preparation of Novel Pyrazolo[4,3-e]tetrazolo[1,5-b][1,2,4]triazine Sulfonamides and Their Experimental and Computational Biological Studies

M Kciuk, S Mujwar, A Szymanowska… - International Journal of …, 2022 - mdpi.com
Pyrazolo [4, 3-e] tetrazolo [1, 5-b][1, 2, 4] triazine sulfonamides constitute a novel class of
heterocyclic compounds with broad biological activity, including anticancer properties …

Structural-based design, synthesis, and antitumor activity of novel alloxazine analogues with potential selective kinase inhibition

WH Malki, AM Gouda, HEA Ali, R Al-Rousan… - European Journal of …, 2018 - Elsevier
Protein kinases are promising therapeutic targets for cancer therapy. Here, we applied
multiple approaches to optimize the potency and selectivity of our reported alloxazine …

Quinazolin-4(3H)-one based potential multiple tyrosine kinase inhibitors with excellent cytotoxicity

TO Mirgany, AN Abdalla, M Arifuzzaman… - Journal of Enzyme …, 2021 - Taylor & Francis
Abstract A series of quinazolin-4 (3 H)-one derivatives were synthesised and evaluated for
their cytotoxicity against human Caucasian breast adenocarcinoma (MCF-7) and human …

One Pot Single Step Synthesis and Biological Evaluation of Some Novel Bis(1,3,4-thiadiazole) Derivatives as Potential Cytotoxic Agents

SM Gomha, NA Kheder, AO Abdelhamid, YN Mabkhot - Molecules, 2016 - mdpi.com
A novel series of bis (1, 3, 4-thiadiazole) derivatives were synthesized in one step
methodology with good yields by condensation reaction between bis-hydrazonoyl chloride 1 …

Design, synthesis and evaluation of new bioactive oxadiazole derivatives as anticancer agents targeting bcl-2

R Hamdy, SA Elseginy, NI Ziedan, M El-Sadek… - International Journal of …, 2020 - mdpi.com
A series of 2-(1 H-indol-3-yl)-5-substituted-1, 3, 4-oxadiazoles, 4a–m, were designed,
synthesized and tested in vitro as potential pro-apoptotic Bcl-2 inhibitory anticancer agents …

Synthesis, antiproliferative, antioxidant activities, in silico studies, DFT analysis and molecular dynamics simulation of novel 1-(4-chlorobenzhydryl) piperazine …

NA Al-Masoudi, RS Jihad, NA Abdul-Rida… - Journal of Molecular …, 2024 - Elsevier
Abstract A series of 1-(4-chlorobenzhydryl) piperazine derivatives 3–10 were synthesized
and characterized both spectroscopically and structurally to investigate their antiproliferative …

Assessment of elementary derivatives of 1, 5-benzodiazepine as anticancer agents with synergy potential

SJ Gawandi, VG Desai, S Joshi, S Shingade… - Bioorganic …, 2021 - Elsevier
Herein, we designed and synthesized 1, 5-benzodiazepines as a lead molecule for
anticancer activity and as potent synergistic activity with drug Methotrexate. Working under …

Synthesis, in silico studies and in vitro cytotoxicity evaluation of novel posaconazole derivative as a ALK TK inhibitor

RD Jawarkar, P Sharma, S Jain, U Shah… - Journal of Taibah …, 2024 - Taylor & Francis
Oncology research progresses, yet cancer remains the largest medical need. The use of a
medication with an accessible lead molecule shows great potential for long-term cancer …