Results 261 to 270 of about 372,460 (343)

Chemical Components of the Dried Latex of Euphorbia resinifera Berg and Its Medicinal Features

open access: yesChemistry &Biodiversity, EarlyView.
ABSTRACT A great deal of research has been carried out on the latex of Euphorbia resinifera Berg, which is an important source of several compounds of therapeutic and medicinal interest. Extraction, synthesis, and hemi synthesis pathways continue to reveal the existence of other new products with anticancer, antioxidant, antidiuretic, and antimalarial ...
Doaa Hammad   +5 more
wiley   +1 more source

Antiaging, Wound‐Healing Properties and Chemical Characterization of Crude Hydroalcoholic Extract and Fractions of Myrcia neoobscura

open access: yesChemistry &Biodiversity, EarlyView.
ABSTRACT The aim of this study was to characterize the phytochemical profile and potential antiaging and wound‐healing activities of 70% hydroalcoholic crude extract (CHE) from Myrcia neoobscura leaves and its fractions—insoluble (IF), ethyl acetate (EAF), and aqueous (AF)—for use in phytocosmetics for skin application.
Larissa Mascarenhas Krepsky   +17 more
wiley   +1 more source

Neutrophils from patients with acquired neutropenia exhibit alterations in serine protease immunostaining and activity. [PDF]

open access: yesBr J Haematol
Mazur A   +6 more
europepmc   +1 more source

A Tailored Phospho‐p53 Library Probes Antibody Specificity and Recognition Limitations

open access: yesChemBioChem, EarlyView.
Site‐specifically phosphorylated isoforms of the tumor suppressor p53 – encompassing all seven known phosphorylation sites within the TAD1 domain –are created upon optimization of semisynthesis protocols. This “designer" p53 library enabled validation of phosphorylation‐specific p53 antibodies and revealed epitope masking by phosphorylation in commonly
Mateusz Hess   +6 more
wiley   +1 more source

Identification of a L‐threonine‐utilizing hydrazine synthetase for thrazarine biosynthesis in Streptomyces coerulescens MH802‐fF5

open access: yesChemBioChem, Accepted Article.
Hydrazine synthetases (HSs), consisting of cupin and methionyl‐tRNA synthetase (MetRS)‐like domains, catalyze hydrazine formation in the biosynthesis of various nitrogen‐nitrogen (N‐N) bond‐containing secondary metabolites. The structural diversity of the N‐N bond‐containing secondary metabolites synthesized using this system is attributed to the ...
Yusuke Shikai   +4 more
wiley   +1 more source

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