Results 171 to 180 of about 111,262 (332)
Cannabinoids From Trema micranthum (L.) Blume (Cannabaceae): A Cannabinoid Profiling System
Chemistry &Biodiversity, EarlyView.ABSTRACT Trema micranthum (L.) Blume is a species from the Cannabaceae botanical family, present all over the tropics. A recent study conducted by our group identified the presence of cannabidiol (CBD), Δ9‐tetrahydrocannabinol, cannabidiolic acid, and tetrahydrocannabinolic acid‐A in T. micranthum extracts.
Yasmin Cunha‐Silva +7 more
wiley +1 more source
Chemistry &Biodiversity, EarlyView.ABSTRACT Yeasts belonging to the genus Rhodotorula are capable of synthesizing carotenoids, such as β‐carotene, γ‐carotene, torulene, torularodine, and astaxanthin. These carotenoids have been shown to offer health benefits to humans, such as immune system strengthening and a reduced risk of chronic degenerative diseases.
David Cristian Rodrigues Lucas +1 more
wiley +1 more source
Chemistry &Biodiversity, EarlyView.Synthesis of 8‐hydroxyquinoline derivatives (QD 1‐12) from different analogues of 8‐hydroxyquinoline (HQ 1‐4). The derivatives and parent compounds were evaluated for antibacterial and antibiofilm activity against Mycobacterium tuberculosis, Mycobacterium smegmatis, methicillin‐resistant Staphylococcus aureus and methicillin‐sensitive Staphylococcus ...
Namrita Lall +9 more
wiley +1 more source
A New Biaryl Synthesis Illustrating a Connection between the Ullmann Biaryl Synthesis and Copper-catalysed Decarboxylation. [PDF]
, 1966 Martin Nilsson +7 more
openalex +1 more source
Exploring Resource Recovery Technologies for Medicinal Cannabis Waste
ChemBioEng Reviews, EarlyView.This review highlights the different types of sustainable treatment methods that are available for medicinal cannabis processing. There are challenges that occur throughout processing, mainly the legislative issues that issues from handling the waste. Several methods are discussed within this article on correctly treating medicinal cannabis waste in a ...
Kerry Jack Robertson +4 more
wiley +1 more source
DETERMINATION OF ASPARTIC AND GLUTAMIC ACIDS BY ENZYMATIC DECARBOXYLATION
, 1951 Alton Meister +2 more
openalex +1 more source
ChemBioChem, EarlyView.2‐oxoglutarate (2OG) analogs are rationally designed to elucidate structure–activity relationships (SARs) in 2OG‐dependent nonheme iron (NHFe) enzymes. These analogs are tested against prolyl hydroxylase domain 2 (PHD2). Activity assays reveal that certain analogs compete with 2OG for the PHD2 active site.
Peter Windsor +3 more
wiley +1 more source
Carbonic acid production and the role of carbonic anhydrase in decarboxylation in brain [PDF]
, 1969 John W. Severinghaus +2 more
openalex +1 more source
Hazelnut: Explorations toward the Biocatalytic Synthesis of its Aroma Precursor
ChemBioChem, EarlyView.This article proposes a biosynthetic route for synthesizing filbertone, the principal flavor compound of hazelnut, through a multienzyme cascade. The pathway uses D‐amino acid oxidase, threonine deaminase, and a regioselective transketolase from Geobacillus stearothermophilus to produce a sustainable, natural hazelnut aroma precursor, addressing ...
Mireia Salvadó‐Pau +3 more
wiley +1 more source
Design and Characterization of Prodrugged Anti‐CTLA‐4 Antibodies
ChemBioChem, Accepted Article.Therapeutic antibodies are widely used to treat diseases like cancer and inflammatory conditions by binding with high specificity to their molecular targets. Masking is a strategy to mitigate undesirable activity in non‐target tissues, improving safety and pharmacokinetic (PK) profiles by reducing target‐mediated drug disposition (TMDD). In this study,
Sayumi Yamazoe +15 more
wiley +1 more source