Results 281 to 290 of about 3,524,198 (392)

Mangiferin potentiates the activity of antifungal agents against fluconazole-resistant <i>Candida</i> spp. [PDF]

Future Microbiol
Ferreira TL, Leitão AC, da Silva LJ, do Amaral Valente Sá LG, de Farias Cabral VP, Rodrigues DS, Barbosa SA, de Andrade Neto JB, Barbosa AD, Almeida Moreira LE, França Rios ME, Cavalcanti BC, de Moraes MO, Nobre Júnior HV, da Silva CR.   +14 more
europepmc   +1 more source

Establishment, Characterization, and Cryopreservation of Feather Follicle Fibroblast Lines From Hyacinth Macaw (Anodorhynchus hyacinthinus)

Cell Biology International, EarlyView.
ABSTRACT Cryopreservation, biobanking, and in vitro propagation of cells from endangered species represent key strategies for advancing biodiversity conservation. The Hyacinth Macaw (Anodorhynchus hyacinthinus), a flagship avian species of the Brazilian Pantanal, is among the critically vulnerable taxa that stand to benefit significantly from such ...
Iara Pastor Martins Nogueira, Rachel Castro Teixeira‐Santos, Gustavo Caldeira Cotta, Wanderson Valente, John Lennon Paiva de Coimbra, Heloísa Athaydes Seabra Ferreira, Pedro Pires Goulart Guimarães, Anderson Kenedy Santos, Fernanda Mussi Fontoura, Kefany Rodrigues de Andrade Ramalho, Neiva Maria Robaldo Guedes, Samyra Maria dos Santos Nassif Lacerda   +11 more
wiley   +1 more source

Small molecule inhibitors of fungal Δ(9) fatty acid desaturase as antifungal agents against Candida auris. [PDF]

Front Cell Infect Microbiol
Tebbji F, Menon ACT, Khemiri I, St-Cyr DJ, Villeneuve L, Vincent AT, Sellam A.   +6 more
europepmc   +1 more source

Sustainable One‐Pot Synthesis of N‐Substituted Pyrroles Using a Multifunctional Cobalt‐Based Catalyst

ChemCatChem, EarlyView.
The one‐pot synthesis of N‐substituted pyrroles from nitrobenzene and 2,5‐hexanodione is first ever reported with >99% conversion and >99% chemoselectivity, in a green solvent, using a non‐noble metal‐based catalyst and hydrogen as a reductant under mild reaction conditions simultaneously.
Jose Luis del Río‐Rodríguez, Arisbeth Tiscareño‐Ferrer, Silvia Gutiérrez‐Tarriño, Pascual Oña‐Burgos   +3 more
wiley   +1 more source

The Efficacy and Safety of Antifungal Agents for Managing Oral Candidiasis in Oncologic Patients: A Systematic Review With Network Meta-Analysis. [PDF]

Cureus
de Lima AF, Fagundes VL, Marques NB, Borba HL, Domingos EL, Tonin FS, Pontarolo R.   +6 more
europepmc   +1 more source

Monoglycerides as an Antifungal Agent

, 2020
Jumina Jumina, Febri Odel Nitbani
openaire   +3 more sources

A New Pentanorlanostane Derivative, Cladosporide A, as a Characteristic Antifungal Agent against Aspergillus fumigatus, Isolated from Cladosporium sp.

, 2000
Tomoo Hosoe, Hideaki Okada, Takeshi Itabashi, Koohei Nozawa, Kaoru Okada, Galba Maria de Campos‐Takaki, Kazutaka Fukushima, Makoto Miyaji, Ken‐ichi Kawai   +8 more
openalex   +2 more sources

CuH‐Catalyzed Asymmetric Desymmetrization of Cyclobutenes via Stereodivergent Hydroamination

ChemistryEurope, EarlyView.
The CuH‐catalyzed stereodivergent hydroamination through asymmetric desymmetrization of cyclobutenes has been achieved, yielding a range of trisubstituted aminocyclobutanes with excellent results. A series of subsequent transformations, including the first asymmetric synthesis of two pharmaceutically active molecules, have been realized, and density ...
Xiang Lei, Peng Luo, Shouang Lan, Wennan Dong, Chao Xu, Jinggong Liu, Shuang Yang, Qi Zhang, Xinqiang Fang   +8 more
wiley   +1 more source

Discovery of semisynthetic derivatives of (<i>R</i>)- and (<i>S</i>)-usnic acids as potential antifungal agents against <i>C. tropicalis</i> and <i>T. rubrum</i>. [PDF]

RSC Med Chem
Fontana A, Colleoni A, Listro R, Rossino G, Linciano P, Vigani B, Valentino C, Cavalloro V, Temporiti MEE, Tosi S, Martino E, Collina S.   +11 more
europepmc   +1 more source

Synthesis of a Functionalized Bicyclo[3.2.1]Octane: A Common Subunit to Kauranes, Grayananes, and Gibberellanes

Chemistry – A European Journal, EarlyView.
A detailed account on the synthesis of a bicyclo[3.2.1]octane scaffold, common to the kaurane, grayanane, and gibberellane diterpenoid families, is reported. Our original strategy relying on a 1,4‐sila‐Prins cyclization proved unsuccessful. Learning from that, we designed an alternative strategy relying on ring‐closing metathesis (RCM), which ...
Nicolas Fay, Camil Benbouziyane, Cyrille Kouklovsky, Aurélien de la Torre   +3 more
wiley   +1 more source