Green chemistry approach towards Piperazine: anticancer agents

V Sharma, R Das, D Sharma, S Mujwar… - Journal of Molecular …, 2023 - Elsevier
Through the exploitation of several conventional strategies in subdisciplines of chemistry
and the molecular sciences became challenging due to toxic chemicals in last few years. As …

Poly (ADP-ribose) polymerase (PARP) inhibitors as anticancer agents: An outlook on clinical progress, synthetic strategies, biological activity, and structure-activity …

PK Das, GSP Matada, R Pal, L Maji, PS Dhiwar… - European Journal of …, 2024 - Elsevier
Abstract Poly (ADP-ribose) polymerase (PARP) is considered an essential component in
case of DNA (Deoxyribonucleic acid) damage, response by sensing DNA damage and …

Synthesis of Azabicyclic Isosteres of Piperazine 2S-Carboxylic Acid

M Vaillancourt, A Mishra, E Duchamp… - The Journal of Organic …, 2024 - ACS Publications
Methods have been developed for the stereocontrolled synthesis of bicyclic diaza [3.3. 0]
octane carboxylic acids as possible isosteres of piperazine 2 S-carboxylic acid. In the first …

Bacterial tyrosinase inhibition, hemolytic and thrombolytic screening, and in silico modeling of rationally designed tosyl piperazine-engrafted dithiocarbamate …

AF Zahoor, F Hafeez, A Mansha, S Kamal, MN Anjum… - Biomedicines, 2023 - mdpi.com
Piperazine is a privileged moiety that is a structural part of many clinical drugs. Piperazine-
based scaffolds have attracted the attention of pharmaceutical and medicinal scientists to …

Discovery of novel tranylcypromine-based derivatives as LSD1 inhibitors for gastric cancer treatment

QS Ma, YF Zhang, CY Li, WX Zhang, L Yuan… - European Journal of …, 2023 - Elsevier
As an important epigenetic regulator, histone lysine specific demethylase 1 (LSD1) has
become an attractive target for the discovery of anticancer agents. In this work, a series of …

Discovery of novel hydroxyimine-tethered benzenesulfonamides as potential human carbonic anhydrase IX/XII inhibitors

MN Peerzada, D Vullo, N Paoletti… - ACS Medicinal …, 2023 - ACS Publications
To discover novel carbonic anhydrase (CA, EC 4.2. 1.1) inhibitors for cancer treatment, a
series of 4-{4-[(hydroxyimino) methyl] piperazin-1-yl} benzenesulfonamides were designed …

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 …

Therapeutic Targeting of Lung Adenocarcinoma with Mannose-Coated Chitosan/Copper Nanocluster–Levocetirizine Nanocomposite

K Choudhury, A Chattopadhyay… - ACS Applied Nano …, 2023 - ACS Publications
Lung adenocarcinoma is regarded as the most common form of lung cancer, per the latest
epidemiological data. The combined efforts from chemotherapy and radiotherapy have done …

Design and synthesis of pyrrolo[2,3-d]pyrimidine linked hybrids as α-amylase inhibitors: molecular docking, MD simulation, ADMET and antidiabetic screening

AR Zala, R Tiwari, HN Naik, I Ahmad, H Patel… - Molecular Diversity, 2024 - Springer
Abstract Novel pyrrolo [2, 3-d] pyrimidine-based analogues were designed, synthesized,
and evaluated for their ability to inhibit the α-amylase enzyme in order to treat diabetes. In …

Novel sulfonamides unveiled as potent anti-lung cancer agents via tumor pyruvate kinase M2 activation

R Das, DR Chatterjee, S Kapoor, H Vyas… - RSC Medicinal …, 2024 - pubs.rsc.org
This rational pursuit led to the identification of a novel sulfonamide derivative as a potent anti-
lung cancer (LC) compound. Considering these results, we synthesized 38 novel …