[HTML][HTML] A New Family of Benzo[h]Chromene Based Azo Dye: Synthesis, In-Silico and DFT Studies with In Vitro Antimicrobial and Antiproliferative Assessment

AS Abd-El-Aziz, A Alsaggaf, E Assirey, A Naqvi… - International Journal of …, 2021 - mdpi.com
The high biological activity of the chromene compounds coupled with the intriguing optical
features of azo chromophores prompted our desire to construct novel derivatives of …

Using computers to ESKAPE the antibiotic resistance crisis

TH da Silva, TZ Hachigian, J Lee, MD King - Drug Discovery Today, 2022 - Elsevier
Since the discovery of penicillin, the development and use of antibiotics have promoted safe
and effective control of bacterial infections. However, the number of antibiotic-resistance …

Synthesis and evaluation of novel 1, 3, 4-thiadiazole--fluoroquinolone hybrids as antibacterial, antituberculosis, and anticancer agents

A Demirci, KG KARAYEL, E Tatar… - Turkish Journal of …, 2018 - journals.tubitak.gov.tr
Abstract A series of 5-substituted-1, 3, 4-thiadiazole-based fluoroquinolone derivatives were
designed as potential antibacterial and anticancer agents using a molecular hybridization …

β-pinene derived products with enhanced in vitro antimicrobial activity

X Feng, Z Xiao, Y Yang, S Chen… - Natural Product …, 2021 - journals.sagepub.com
The development of new antimicrobials has always been a research hotspot. In this study, β-
pinene-based derivatives were synthesized, and their antimicrobial activity was evaluated …

Quantitative structure–activity relationship methods in the discovery and development of antibacterials

B Suay‐Garcia, JI Bueso‐Bordils… - Wiley …, 2020 - Wiley Online Library
With the pressing issue of antibiotic resistance, there is a constant need for new antibiotics.
However, the fact that traditional methods of drug discovery are expensive and time …

Synthesis, characterization, molecular modeling, and potential antimicrobial and anticancer activities of novel 2-aminoisoindoline-1, 3-dione derivatives

HEA Ahmed, HA Abdel-Salam, MA Shaker - Bioorganic Chemistry, 2016 - Elsevier
In an effort to establish new drug candidates with improved antimicrobial and anticancer
activities, we report here synthesis, molecular modeling, and in vitro biological evaluation of …

Chromanyl–isoxazolidines as antibacterial agents: synthesis, biological evaluation, quantitative structure activity relationship, and molecular docking studies

G Singh, A Sharma, H Kaur… - Chemical biology & drug …, 2016 - Wiley Online Library
Regio‐and stereoselective 1, 3‐dipolar cycloadditions of C‐(chrom‐4‐one‐3‐yl)‐N‐
phenylnitrones (N) with different mono‐substituted, disubstituted, and cyclic dipolarophiles …

Synthesis and comparative carbonic anhydrase inhibition of new Schiff's bases incorporating benzenesulfonamide, methanesulfonamide, and methylsulfonylbenzene …

AS El-Azab, AM Alaa, S Bua, A Nocentini… - Bioorganic …, 2019 - Elsevier
Herein, we report the synthesis, characterization, and carbonic anhydrase (CA) inhibition of
the newly synthesized Schiff's bases 4–18 with benzenesulfonamide, methanesulfonamide …

[HTML][HTML] Poly (3-hydroxybutyrate)/poly (amine)-coated nickel oxide nanoparticles for norfloxacin delivery: antibacterial and cytotoxicity efficiency

N Salahuddin, M Gaber, M Mousa, MA Abdelwahab - RSC advances, 2020 - pubs.rsc.org
Sustained release dosage forms enable prolonged and continuous release of a drug in the
gastrointestinal tract for medication characterized by a short half lifetime. In this study, the …

4‐Quinolone Derivatives and Their Activities Against Gram‐negative Pathogens

D Jiang - Journal of Heterocyclic Chemistry, 2018 - Wiley Online Library
Gram‐negative pathogens represent a significant global health threat, while the emergency
and widespread of drug resistance make the situation even worse. As “privileged building …