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 …
available intermediates in organic synthesis, including total synthesis of natural products. 1 …
Medicinal chemistry of oxazines as promising agents in drug discovery
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 …
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 …
hepatocellular carcinoma (HCC), and blockade of NF-κB signaling could be a potential …
Novel synthetic coumarins that targets NF-κB in Hepatocellular carcinoma
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 …
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
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 …
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 …
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 …
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 …
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 …
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 …
new difluoromethylated analogs of imidazolidinone-based PDE4 inhibitor CMPI in a …