1-Piperazinylphthalazines as potential VEGFR-2 inhibitors and anticancer agents: synthesis and in vitro biological evaluation
… the development of effective VEGFR-2 inhibitors, three … evaluated in vitro for their inhibitory
activity against VEGFR-2. In particular, compounds 16k and 21d potently inhibited VEGFR-2 …
activity against VEGFR-2. In particular, compounds 16k and 21d potently inhibited VEGFR-2 …
Design, synthesis and biological evaluation of type-II VEGFR-2 inhibitors based on quinoxaline scaffold
MI Shahin, DA Abou El Ella, NSM Ismail… - Bioorganic …, 2014 - Elsevier
… In an effort to develop ATP-competitive VEGFR-2 selective inhibitors, a series of new … The
target compounds were biologically evaluated for their inhibitory activity against VEGFR-2. The …
target compounds were biologically evaluated for their inhibitory activity against VEGFR-2. The …
Design, synthesis and biological evaluation of N-phenylquinazolin-4-amine hybrids as dual inhibitors of VEGFR-2 and HDAC
FW Peng, J Xuan, TT Wu, JY Xue, ZW Ren… - European journal of …, 2016 - Elsevier
… VEGFR-2/HDAC inhibitors. Compound 6fd exhibited the most potent inhibitory activity against
HDAC with IC 50 of 2.2 nM and strong inhibitory effect against VEGFR-2 … of VEGFR-2 and …
HDAC with IC 50 of 2.2 nM and strong inhibitory effect against VEGFR-2 … of VEGFR-2 and …
Indoline ureas as potential anti-hepatocellular carcinoma agents targeting VEGFR-2: Synthesis, in vitro biological evaluation and molecular docking
In our effort to develop potent and effective agents with anti-proliferative activity towards HepG2
hepatocellular carcinoma cells with potential inhibitory activity against VEGFR-2, a novel …
hepatocellular carcinoma cells with potential inhibitory activity against VEGFR-2, a novel …
Novel 5-anilinoquinazoline-8-nitro derivatives as inhibitors of VEGFR-2 tyrosine kinase: synthesis, biological evaluation and molecular docking
L Xi, JQ Zhang, ZC Liu, JH Zhang, JF Yan… - Organic & Biomolecular …, 2013 - pubs.rsc.org
Vascular endothelial growth factor receptor-2 (VEGFR-2) kinase inhibition is a well-established
strategy to promptly tackle tumor growth by suppression of angiogenesis. We report …
strategy to promptly tackle tumor growth by suppression of angiogenesis. We report …
Identification of new theobromine-based derivatives as potent VEGFR-2 inhibitors: design, semi-synthesis, biological evaluation, and in silico studies
This study aimed to design anticancer theobromine derivatives inhibiting VEGFR-2. The new
compounds were tested in vitro to evaluate their effectiveness against MCF-7 and HepG2 …
compounds were tested in vitro to evaluate their effectiveness against MCF-7 and HepG2 …
Synthesis and biological evaluation of glycyrrhetic acid derivatives as potential VEGFR2 inhibitors
TL Yan, LF Bai, HL Zhu, WM Zhang, PC Lv - ChemMedChem, 2017 - Wiley Online Library
… Vascular endothelial growth factor receptor 2 (VEGFR2) has … synthesized and evaluated for
their VEGFR2 inhibitory activity as … In vitro biological evaluations against these human tumor …
their VEGFR2 inhibitory activity as … In vitro biological evaluations against these human tumor …
… , in silico studies, and biological evaluation of novel pyrimidine-5-carbonitrile derivatives as potential anti-proliferative agents, VEGFR-2 inhibitors and apoptotic …
AM Saleh, HA Mahdy, MA El-Zahabi, ABM Mehany… - RSC …, 2023 - pubs.rsc.org
… pyrimidine derivatives as potential VEGFR-2 TK inhibitors. Observing the results of different
biological tests (in vitro anti-proliferative activity, measurement of VEGFR-2 TK activity), we …
biological tests (in vitro anti-proliferative activity, measurement of VEGFR-2 TK activity), we …
… of Novel Cyanopyridones and Pyrido[2,3-d]pyrimidines as Anticancer Agents with Dual VEGFR-2/HER-2 Inhibitory Action: Synthesis, Biological Evaluation and …
In the current work, we designed and synthesized three families of non-fused and fused
compounds based on cyanopyridone: derivatives of 6-amino-1,2-dihydropyridine-3,5-…
compounds based on cyanopyridone: derivatives of 6-amino-1,2-dihydropyridine-3,5-…
Synthesis and Biological Evaluation of Novel Oxazolo[5,4‐d]pyrimidines as Potent VEGFR‐2 Inhibitors
YH Deng, D Xu, YX Su, YJ Cheng… - Chemistry & …, 2015 - Wiley Online Library
… good potency against VEGFR-2 (IC50 … biological evaluations against multiple kinases (Table
2). Compounds 9d and 9o exhibited selective inhibitory activities against VEGFR-2, VEGFR-…
2). Compounds 9d and 9o exhibited selective inhibitory activities against VEGFR-2, VEGFR-…