Recent accomplishments on the synthetic/biological facets of pharmacologically active 1H-1, 2, 3-triazoles

S Kumar, B Sharma, V Mehra, V Kumar - European Journal of Medicinal …, 2021 - Elsevier
The continuous demand of medicinally important scaffolds has prompted the synthetic
chemists to identify simple and efficient routes for their synthesis. 1H-1, 2, 3-triazole …

Screening approaches and therapeutic targets: The two driving wheels of tuberculosis drug discovery

S Perveen, R Sharma - Biochemical Pharmacology, 2022 - Elsevier
Tuberculosis (TB) is an infectious disease, infecting a quarter of world's population. Drug
resistant TB further exacerbates the grim scenario of the drying TB drug discovery pipeline …

A specific inhibitor of ALDH1A3 regulates retinoic acid biosynthesis in glioma stem cells

J Li, S Garavaglia, Z Ye, A Moretti, OV Belyaeva… - Communications …, 2021 - nature.com
Elevated aldehyde dehydrogenase (ALDH) activity correlates with poor outcome for many
solid tumors as ALDHs may regulate cell proliferation and chemoresistance of cancer stem …

Chitosan Schiff bases-based polyelectrolyte complexes with graphene quantum dots and their prospective biomedical applications

AA Hamed, GR Saad, IA Abdelhamid… - International Journal of …, 2022 - Elsevier
Abstract Chitosan (Cs) bis-aldehyde Schiff base derivatives were synthesized by
condensation of Cs with three bis-aldehydes namely; butane-1, 4-diyl bis (4 …

Design and synthesis of triazole conjugated novel 2, 5-diaryl substituted 1, 3, 4-oxadiazoles as potential antimicrobial and anti-fungal agents

S Bitla, SR Sagurthi, R Dhanavath… - Journal of Molecular …, 2020 - Elsevier
A series of triazole conjugated novel 2, 5-diaryl 1, 3, 4-oxadiazole derivatives 8a-q are
efficiently synthesized starting from methyl salicylate. All the synthesized compounds were …

[HTML][HTML] Synthesis and structure–activity relationship of 1-(5-isoquinolinesulfonyl) piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH

V Singh, A Pacitto, S Donini, DM Ferraris… - European journal of …, 2019 - Elsevier
Tuberculosis (TB) is a major infectious disease associated increasingly with drug resistance.
Thus, new anti-tubercular agents with novel mechanisms of action are urgently required for …

Targeting Genome Integrity in Mycobacterium Tuberculosis: From Nucleotide Synthesis to DNA Replication and Repair

R Miggiano, C Morrone, F Rossi, M Rizzi - Molecules, 2020 - mdpi.com
Mycobacterium tuberculosis (MTB) is the causative agent of tuberculosis (TB), an ancient
disease which still today causes 1.4 million deaths worldwide per year. Long-term, multi …

Inhibitors of inosine 5′-monophosphate dehydrogenase as emerging new generation antimicrobial agents

K Juvale, A Shaik, S Kirubakaran - Medchemcomm, 2019 - pubs.rsc.org
Inosine 5′-monophosphate dehydrogenase (IMPDH) is a vital enzyme involved in the de
novo synthesis of guanine nucleotides. IMPDH catalyzes a crucial step of converting IMP …

Discovery of novel human inosine 5′-monophosphate dehydrogenase 2 (hIMPDH2) inhibitors as potential anticancer agents

CP Shah, PS Kharkar - European journal of medicinal chemistry, 2018 - Elsevier
The enzyme inosine 5′-monophosphate dehydrogenase (IMPDH) catalyzes an essential
step in the de novo biosynthesis of guanine nucleotides, and thus regulates the guanine …

Development, synthesis, and biological evaluation of sulfonyl‐α‐l‐amino acids as potential anti‐Helicobacter pylori and IMPDH inhibitors

AMF Galal, HS Mohamed, MM Abdel‐Aziz… - Archiv der …, 2021 - Wiley Online Library
Inosine 5ʹ‐monophosphate dehydrogenase (IMPDH) catalyzes a crucial step in the
biosynthesis of DNA and RNA, and it has been exploited as a promising target for …