Benzophenone: A ubiquitous scaffold in medicinal chemistry
K Surana, B Chaudhary, M Diwaker, S Sharma - MedChemComm, 2018 - pubs.rsc.org
The benzophenone scaffold represents a ubiquitous structure in medicinal chemistry
because it is found in several naturally occurring molecules which exhibit a variety of …
because it is found in several naturally occurring molecules which exhibit a variety of …
Anticancer mechanism of coumarin-based derivatives
AK Yadav, RM Shrestha, PN Yadav - European Journal of Medicinal …, 2024 - Elsevier
The structural motif of coumarins is related with various biological activities and
pharmacological properties. Both natural coumarin extracted from various plants or a new …
pharmacological properties. Both natural coumarin extracted from various plants or a new …
Green synthesis and evaluation of antiangiogenic, photocatalytic, and electrochemical activities of BiVO4 nanoparticles
C Mallikarjunaswamy, S Pramila, G Nagaraju… - Journal of Materials …, 2021 - Springer
Nanocrystalline bismuth vanadate has been steadily gaining attention in recent years due to
its potential energy conversion and eco-friendly nature. Herein, we report the green …
its potential energy conversion and eco-friendly nature. Herein, we report the green …
Synthesis and tumor inhibitory activity of novel coumarin analogs targeting angiogenesis and apoptosis
A sequence of coumarin analogs 5a–j was obtained by multi step synthesis from hydroxy
benzophenones (1a–j). The in vitro antiproliferative effect of the title compounds was tested …
benzophenones (1a–j). The in vitro antiproliferative effect of the title compounds was tested …
Polyphenols with Antiulcerogenic Action from Aqueous Decoction of Mango Leaves (Mangifera indica L.)
This study was designed to determine the gastroprotective effect of a Mangifera indica leaf
decoction (AD), on different experimental models in rodents. The administration of AD up to …
decoction (AD), on different experimental models in rodents. The administration of AD up to …
Growth inhibition and pro-apoptotic activity of violacein in Ehrlich ascites tumor
N Bromberg, JL Dreyfuss, CV Regatieri… - Chemico-biological …, 2010 - Elsevier
The continuing threat to biodiversity lends urgency to the need of identification of
sustainable source of natural products. This is not so much trouble if there is a microbial …
sustainable source of natural products. This is not so much trouble if there is a microbial …
BP-1T, an antiangiogenic benzophenone-thiazole pharmacophore, counteracts HIF-1 signalling through p53/MDM2-mediated HIF-1α proteasomal degradation
Hypoxia is a feature of all solid tumours, contributing to tumour progression. Activation of HIF-
1α plays a critical role in promoting tumour angiogenesis and metastasis. Since its …
1α plays a critical role in promoting tumour angiogenesis and metastasis. Since its …
Targeting HIF-1α by newly synthesized Indolephenoxyacetamide (IPA) analogs to induce anti-angiogenesis-mediated solid tumor suppression
FH Al-Ostoot, A Sherapura, VV, G Basappa… - Pharmacological …, 2021 - Springer
Background Hypoxic microenvironment is a common feature of solid tumors, which leads to
the promotion of cancer. The transcription factor, HIF-1α, expressed under hypoxic …
the promotion of cancer. The transcription factor, HIF-1α, expressed under hypoxic …
A tumoural angiogenic gateway blocker, Benzophenone-1B represses the HIF-1α nuclear translocation and its target gene activation against neoplastic progression
Hypoxia is an important module in all solid tumours to promote angiogenesis, invasion and
metastasis. Stabilization and subsequent nuclear localization of HIF-1α subunits result in the …
metastasis. Stabilization and subsequent nuclear localization of HIF-1α subunits result in the …
Synthesis, characterization and antibacterial activity of 2-[1-(5-chloro-2-methoxy-phenyl)-5-methyl-1H-pyrazol-4-yl]-5-(substituted-phenyl)-[1, 3, 4] oxadiazoles
NP Rai, VK Narayanaswamy, S Shashikanth… - European journal of …, 2009 - Elsevier
In the present investigation a series of novel 2-[1-(5-chloro-2-methoxy-phenyl)-5-methyl-1H-
pyrazol-4-yl]-5-(substituted-phenyl)-[1, 3, 4] oxadiazoles (4a–j) were synthesized by …
pyrazol-4-yl]-5-(substituted-phenyl)-[1, 3, 4] oxadiazoles (4a–j) were synthesized by …