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 …

Novel 1, 3, 4-oxadiazole induces anticancer activity by targeting NF-κB in hepatocellular carcinoma cells

CD Mohan, NC Anilkumar, S Rangappa… - Frontiers in …, 2018 - frontiersin.org
Aberrant activation of NF-κB is linked with the progression of human malignancies including
hepatocellular carcinoma (HCC), and blockade of NF-κB signaling could be a potential …

Novel synthetic coumarins that targets NF-κB in Hepatocellular carcinoma

M Neelgundmath, KR Dinesh, CD Mohan, F Li… - Bioorganic & medicinal …, 2015 - Elsevier
Hepatocellular carcinoma (HCC) is the fifth most common malignant tumor worldwide, and is
the third most common cause of cancer related death. Constitutive activation of NF-κB is the …

Synthesis and characterization of novel 2-amino-chromene-nitriles that target Bcl-2 in acute myeloid leukemia cell lines

HK Keerthy, M Garg, CD Mohan, V Madan, D Kanojia… - PloS one, 2014 - journals.plos.org
The anti-apoptotic protein Bcl-2 is a well-known and attractive therapeutic target for cancer.
In the present study the solution-phase T3P-DMSO mediated efficient synthesis of 2-amino …

Nano-Zirconium Dioxide Catalyzed Multicomponent Synthesis of Bioactive Pyranopyrazoles That Target Cyclin Dependent Kinase 1 in Human Breast Cancer Cells

B Basappa, LK Poonacha, Z Xi, D Vishwanath… - Biomedicines, 2023 - mdpi.com
Small molecules are being used to inhibit cyclin dependent kinase (CDK) enzymes in
cancer treatment. There is evidence that CDK is a drug-target for cancer therapy across …

Synthesis and characterization of novel oxazines and demonstration that they specifically target cyclooxygenase 2

V Srinivas, CD Mohan, CP Baburajeev… - Bioorganic & Medicinal …, 2015 - Elsevier
In the present study, we used solution combustion synthesis-bismuth oxide (Bi 2 O 3) as
catalyst for the simple and efficient synthesis of 1, 2-oxazine based derivatives of 6-fluoro-3 …

Preparation and use of combustion-derived Bi 2 O 3 for the synthesis of heterocycles with anti-cancer properties by Suzuki-coupling reactions

S Anusha, BS Anandakumar, CD Mohan… - RSC …, 2014 - pubs.rsc.org
Bismuth oxide was synthesized via simple, rapid and energy efficient solution combustion
synthesis (SCS) by employing sucrose as a fuel. This SCS-Bi2O3 was characterized by …

[HTML][HTML] Identification of a novel 1, 2 oxazine that can induce apoptosis by targeting NF-κB in hepatocellular carcinoma cells

C Somu, CD Mohan, S Ambekar, S Rangappa… - Biotechnology …, 2020 - Elsevier
Constitutive activation of NF-κB is associated with proinflammatory diseases and
suppression of the NF-κB signaling pathway has been considered as an effective …

Diastereoselective synthesis and profiling of bicyclic imidazolidinone derivatives bearing a difluoromethylated catechol unit as potent phosphodiesterase 4 inhibitors

VS Dorokhov, IS Golovanov, VA Tartakovsky… - Organic & …, 2018 - pubs.rsc.org
Metal-mediated C–H functionalization of cyclic N-oxides was exploited to access a series of
new difluoromethylated analogs of imidazolidinone-based PDE4 inhibitor CMPI in a …