Mechanism of Candida pathogenesis: revisiting the vital drivers

IE Mba, EI Nweze - European Journal of Clinical Microbiology & Infectious …, 2020 - Springer
Candida is the most implicated fungal pathogen in the clinical setting. Several factors play
important roles in the pathogenesis of Candida spp. Multiple transcriptional circuits …

Virulence and biofilms as promising targets in developing antipathogenic drugs against candidiasis

MS Ahmad Khan, F Alshehrei, SB Al-Ghamdi… - Future science …, 2020 - Taylor & Francis
Candida albicans has remained the main etiological agent of candidiasis, challenges
clinicians with high mortality and morbidity. The emergence of resistance to antifungal drugs …

Potential targets for antifungal drug discovery based on growth and virulence in Candida albicans

X Li, Y Hou, L Yue, S Liu, J Du… - Antimicrobial agents and …, 2015 - Am Soc Microbiol
Fungal infections, especially infections caused by Candida albicans, remain a challenging
problem in clinical settings. Despite the development of more-effective antifungal drugs, their …

Inhibition of CpLIP2 lipase hydrolytic activity by four flavonols (galangin, kaempferol, quercetin, myricetin) compared to orlistat and their binding mechanisms studied …

R Nasri, LPR Bidel, N Rugani, V Perrier, F Carrière… - Molecules, 2019 - mdpi.com
The inhibition of recombinant CpLIP2 lipase/acyltransferase from Candida parapsiolosis
was considered a key model for novel antifungal drug discovery and a potential therapeutic …

Investigating virulence factors of clinical Candida isolates in relation to atmospheric conditions and genotype

M Inci, MA Atalay, AN KOÇ, E Yula… - Turkish Journal of …, 2012 - journals.tubitak.gov.tr
To investigate some virulence factors in Candida species isolated from patients with
suspected invasive fungal infection and to identify their relationship with Candida …

α-Glucosidase inhibitors: consistency of in silico docking data with in vitro inhibitory data and inhibitory effect prediction of quercetin derivatives

J Zhu, B Zhang, C Tan, Q Huang - Food & function, 2019 - pubs.rsc.org
The present study aims to investigate the relationship between in silico experimental data
and in vitro inhibitory data of polyphenols against α-glucosidase. The CDOCKER protocol in …

Molecular recognition between pancreatic lipase and natural and synthetic inhibitors

M Bello, L Basilio-Antonio, J Fragoso-Vázquez… - International journal of …, 2017 - Elsevier
Pancreatic lipase (PL) is a primary lipase critical for triacylglyceride digestion in humans and
is considered as a promising target for the treatment of obesity. Although the current …

Synthesis, structure and impact of 5-aminoorotic acid and its complexes with Lanthanum (III) and Gallium (III) on the activity of xanthine oxidase

L Todorov, L Saso, K Benarous, M Traykova, A Linani… - Molecules, 2021 - mdpi.com
The superoxide radical ion is involved in numerous physiological processes, associated
with both health and pathology. Its participation in cancer onset and progression is well …

The inhibitory kinetics of vitamins B9, C, E, and D3 on bovine xanthine oxidase: gout treatment

A Linani, K Benarous, L Bou-Salah, M Yousfi - Chemico-Biological …, 2022 - Elsevier
Background Over-consumption of foods high in purines like seafood, red meat, and
alcoholic beverages leads to hyperuricemia causing gout attacks. Xanthine oxidase was …

Stereochemical structure activity relationship studies (S-SAR) of tetrahydrolipstatin

X Liu, Y Wang, RI Duclos Jr… - ACS Medicinal Chemistry …, 2018 - ACS Publications
Tetrahydrolipstatin (THL), its enantiomer, and an additional six diastereomers were
evaluated as inhibitors of the hydrolysis of p-nitrophenyl butyrate by porcine pancreatic …