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 …

[HTML][HTML] The Structure–Antiproliferative Activity Relationship of Pyridine Derivatives

AL Villa-Reyna, M Perez-Velazquez… - International Journal of …, 2024 - mdpi.com
Pyridine, a compound with a heterocyclic structure, is a key player in medicinal chemistry
and drug design. It is widely used as a framework for the design of biologically active …

[HTML][HTML] Synthesis, docking and biological evaluation of thiadiazole and oxadiazole derivatives as antimicrobial and antioxidant agents

MJN Khadri, AB Begum, MK Sunil, SA Khanum - Results in Chemistry, 2020 - Elsevier
A series of potential biological active substituted thiadiazoles 5a-j and oxadiazoles 6a-j were
obtained via a multistep synthesis sequence with a simple and convenient approach by …

Design, synthesis, characterization, docking studies of novel 4-phenyl acrylamide-1, 3-thiazole derivatives as anti-inflammatory and anti-ulcer agents

HM Pallavi, FH Al-Ostoot, VH Kameshwar… - Journal of Molecular …, 2023 - Elsevier
A great extent of nitrogen containing heterocyclic moiety comprising sulfur atom is
recognized as a valuable combination of therapeutics in medicinal chemistry. In particular …

BP-1T, an antiangiogenic benzophenone-thiazole pharmacophore, counteracts HIF-1 signalling through p53/MDM2-mediated HIF-1α proteasomal degradation

P Thirusangu, V Vigneshwaran, T Prashanth… - Angiogenesis, 2017 - Springer
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 …

Quinoline-and Isoindoline-Integrated Polycyclic Compounds as Antioxidant, and Antidiabetic Agents Targeting the Dual Inhibition of α-Glycosidase and α-Amylase …

M Al-Ghorbani, O Alharbi, AB Al-Odayni, NAY Abduh - Pharmaceuticals, 2023 - mdpi.com
Novel analogs of quinoline and isoindoline containing various heterocycles, such as
tetrazole, triazole, pyrazole, and pyridine, were synthesized and characterized using FT-IR …

A tumoural angiogenic gateway blocker, Benzophenone-1B represses the HIF-1α nuclear translocation and its target gene activation against neoplastic progression

P Thirusangu, V Vigneshwaran, VL Ranganatha… - Biochemical …, 2017 - Elsevier
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 …

The Golgi apparatus may be a potential therapeutic target for apoptosis-related neurological diseases

Q He, H Liu, S Deng, X Chen, D Li, X Jiang… - Frontiers in cell and …, 2020 - frontiersin.org
Increasing evidence shows that, in addition to the classical function of protein processing
and transport, the Golgi apparatus (GA) is also involved in apoptosis, one of the most …

[PDF][PDF] Dalton's lymphoma as a murine model for understanding the progression and development of t-cell lymphoma and its role in drug discovery

RK Koiri, A Mehrotra, SK Trigun - Int j immunother cancer res, 2017 - researchgate.net
Mouse models are irreplaceable tools for the study of carcinogenesis and the availability of
rodent models have enabled rational screening of drugs. Hematological malignancies have …

Synthesis, crystal structure and 3D energy frameworks of ethyl 2-[5-nitro-2-oxopyridine-1 (2H)-yl] acetate: Hirshfeld surface analysis and DFT calculations

K Kumara, FH Al-Ostoot, YHE Mohammed… - Chemical Data …, 2019 - Elsevier
Pyridine derivatives with different heterocyclic nucleus have shown potent pharmacological
properties as a part from the previously marketed drugs. The title compound, ethyl 2-[5-nitro …