Pyrazole-based analogs as potential antibacterial agents against methicillin-resistance staphylococcus aureus (MRSA) and its SAR elucidation

R Verma, SK Verma, KP Rakesh, YR Girish… - European journal of …, 2021 - Elsevier
Methicillin-resistant Staphylococcus aureus (MRSA) is becoming lethal to humanity due to
easy transmission and difficult-to-treat skin and flimsy diseases. The most threatening aspect …

Endophytic fungi—alternative sources of cytotoxic compounds: a review

F Uzma, CD Mohan, A Hashem, NM Konappa… - Frontiers in …, 2018 - frontiersin.org
Cancer is a major cause of death worldwide, with an increasing number of cases being
reported annually. The elevated rate of mortality necessitates a global challenge to explore …

Heterogeneous graphitic carbon nitrides in visible-light-initiated organic transformations

SK Verma, R Verma, YR Girish, F Xue, L Yan… - Green …, 2022 - pubs.rsc.org
In recent years, g-C3N4 photocatalyst-mediated organic reactions have represented an
important mode of chemical transformations and are expected to become a crucial field at …

Cyclooxygenase-2 inhibitors as a therapeutic target in inflammatory diseases

MD Ferrer, C Busquets-Cortés, X Capó… - Current medicinal …, 2019 - ingentaconnect.com
Inflammation plays a crucial role in the development of many complex diseases and
disorders including autoimmune diseases, metabolic syndrome, neurodegenerative …

A key review on oxadiazole analogs as potential methicillin-resistant Staphylococcus aureus (MRSA) activity: Structure-activity relationship studies

SK Verma, R Verma, KSS Kumar, L Banjare… - European journal of …, 2021 - Elsevier
Methicillin-resistant Staphylococcus aureus (MRSA) is becoming dangerous to human
beings due to easy transmission mode and leading to the difficult-to-treat situation. The rapid …

Benzimidazole analogues as efficient arsenals in war against methicillin-resistance staphylococcus aureus (MRSA) and its SAR studies

GF Zha, HD Preetham, S Rangappa, KSS Kumar… - Bioorganic …, 2021 - Elsevier
Small molecule based inhibitors development is a growing field in medicinal chemistry. In
recent years, different heterocyclic derivatives have been designed to counter the infections …

Structure-activity relationship studies of thiazole agents with potential anti methicillin-resistance Staphylococcus aureus (MRSA) activity

J Wang, S Long, Z Liu, KP Rakesh, R Verma… - Process …, 2023 - Elsevier
Due to the increasing resistance of methicillin-resistant Staphylococcus aureus (MRSA) to
conventional antibiotics, further efforts are needed to develop new antimicrobial agents …

Stereoselective reactions of nitro compounds in the synthesis of natural compound analogs and active pharmaceutical ingredients

AY Sukhorukov, AA Sukhanova, SG Zlotin - Tetrahedron, 2016 - Elsevier
Nitroalkanes and nitroalkenes have been always considered as convenient and readily
available intermediates in organic synthesis, including total synthesis of natural products. 1 …

Medicinal chemistry of oxazines as promising agents in drug discovery

DS Zinad, A Mahal, RK Mohapatra… - Chemical biology & …, 2020 - Wiley Online Library
Oxazines have brought much synthetic interest due to their extensive biological activities.
These are the important category of heterocycles, which may be formally derived from …

Targeting heparanase in cancer: inhibition by synthetic, chemically modified, and natural compounds

CD Mohan, S Hari, HD Preetham, S Rangappa… - Iscience, 2019 - cell.com
Heparanase is an endoglycosidase involved in remodeling the extracellular matrix and
thereby in regulating multiple cellular processes and biological activities. It cleaves heparan …