Pyrrole: An emerging scaffold for construction of valuable therapeutic agents

SS Gholap - European journal of medicinal chemistry, 2016 - Elsevier
Pyrrole derivatives comprise a class of biologically active heterocyclic compounds which
can serve as promising scaffolds for antimicrobial, antiviral, antimalarial, antitubercular, anti …

The Role of VEGF receptors as molecular target in nuclear medicine for cancer diagnosis and combination therapy

K Masłowska, PK Halik, D Tymecka, A Misicka… - Cancers, 2021 - mdpi.com
Simple Summary The rapid development of diagnostic and therapeutic methods of the
cancer treatment causes that these diseases are becoming better known and the fight …

Design and synthesis of pyrazole–oxindole conjugates targeting tubulin polymerization as new anticancer agents

A Kamal, AB Shaik, N Jain, C Kishor… - European journal of …, 2015 - Elsevier
A series of twenty one compounds with pyrazole and oxindole conjugates were synthesized
by Knoevenagel condensation and investigated for their antiproliferative activity on different …

3-Alkenyl-2-oxindoles: Synthesis, antiproliferative and antiviral properties against SARS-CoV-2

AS Girgis, SS Panda, AM Srour, A Abdelnaser… - Bioorganic …, 2021 - Elsevier
Abstract Sets of 3-alkenyl-2-oxindoles (6, 10, 13) were synthesized in a facile synthetic
pathway through acid dehydration (EtOH/HCl) of the corresponding 3-hydroxy-2 …

Synthesis and initial preclinical evaluation of the P2X7 receptor antagonist [11C]A‐740003 as a novel tracer of neuroinflammation

B Janssen, DJ Vugts, U Funke… - Journal of Labelled …, 2014 - Wiley Online Library
Neuroinflammation, in particular activation of microglia, is thought to play an important role
in the progression of neurodegenerative diseases. In activated microglia, the purinergic …

Exploration for novel inhibitors showing back-to-front approach against VEGFR-2 kinase domain (4AG8) employing molecular docking mechanism and molecular …

S Rampogu, A Baek, A Zeb, KW Lee - BMC cancer, 2018 - Springer
Background Angiogenesis is a process of formation of new blood vessels and is an
important criteria demonstrated by cancer cells. Over a period of time, these cancer cells …

Design, synthesis and biological evaluation of 1, 4-dihydro indeno [1, 2-c] pyrazole linked oxindole analogues as potential anticancer agents targeting tubulin and …

I Khan, KR Garikapati, AB Shaik, VKK Makani… - European Journal of …, 2018 - Elsevier
Abstract A series of 1, 4-dihydroindeno-[1, 2-c] pyrazole linked oxindole conjugates have
been synthesized by using Knoevenagel condensation method and further evaluated for …

Novel receptor tyrosine kinase pathway inhibitors for targeted radionuclide therapy of glioblastoma

J Bolcaen, S Nair, CHS Driver, TMG Boshomane… - Pharmaceuticals, 2021 - mdpi.com
Glioblastoma (GB) remains the most fatal brain tumor characterized by a high infiltration rate
and treatment resistance. Overexpression and/or mutation of receptor tyrosine kinases is …

An expedient synthesis of C3-arylidene-oxindole derivatives using calcite nanoflowers as an efficient heterogeneous catalyst

D Sanap, L Avhad, S Ghotekar, ND Gaikwad - Inorganic Chemistry …, 2023 - Elsevier
Abstract α-β unsaturated heterocyclic compounds such as C3-arylidene-oxindoles, with five-
member rings containing nitrogen, have an important role in the realm of medicine. This …

Discovery of N-(2-phenyl-1H-benzo [d] imidazol-5-yl) quinolin-4-amine derivatives as novel VEGFR-2 kinase inhibitors

L Shi, TT Wu, Z Wang, JY Xue, YG Xu - European Journal of Medicinal …, 2014 - Elsevier
Inhibition of the VEGF signaling pathway has become a valuable approach in the treatment
of cancers. In this work, a series of N-(2-phenyl-1H-benzo [d] imidazol-5-yl) quinolin-4-amine …