Differential Effects of Non-Microbial Biostimulants on Secondary Metabolites and Nitrate Content in Organic Arugula Leaves. [PDF]
Ciriello M +8 more
europepmc +1 more source
Sulforaphane Synergies with Phytochemicals and Pharmaceuticals: Implications for Healthspan. [PDF]
Fahey JW, Liu H.
europepmc +1 more source
Extracellular DNA triggers glucosinolate-dependent defence responses against Frankliniella occidentalis. [PDF]
Rassizadeh L +4 more
europepmc +1 more source
Exosome-like nanovesicles derived from kale juice enhance collagen production by downregulating Smad7 in human skin fibroblasts. [PDF]
Hsu P +6 more
europepmc +1 more source
Quantitative dissection of Agrobacterium T-DNA expression in single plant cells reveals density-dependent synergy and antagonism. [PDF]
Alamos S +12 more
europepmc +1 more source
Elucidation of Sulforaphane-Mediated Effects on the Cellular Human Metabolome Using Metabolic Profiling. [PDF]
Bieß N +3 more
europepmc +1 more source
Evolution of Secondary Metabolites in <i>Eruca sativa</i> from the Microgreen to the Reproductive Stage: An Integrative Multi-Platform Metabolomics Approach. [PDF]
Monzillo F +7 more
europepmc +1 more source
Analysis of Different Parts of Broccoli (<i>Brassica oleracea</i> var. <i>italica</i>) Leaves and Retention of Functional Compounds Under Different Cooking Methods. [PDF]
Kim MG, Park JH, Joo N.
europepmc +1 more source
Bioavailability of Glucoraphanin and Sulforaphane from High‐Glucoraphanin Broccoli [PDF]
ScopeBroccoli accumulates 4‐methylsulphinylbutyl glucosinolate (glucoraphanin) which is hydrolyzed to the isothiocyanate sulforaphane. Through the introgression of novel alleles of the Myb28 transcription factor from Brassica villosa, broccoli genotypes have been developed that have enhanced levels of glucoraphanin.
Antonietta Melchini +2 more
exaly +7 more sources
The synthesis of isotopically labelled glucoraphanin for metabolic studies
Abstract The first synthesis of a stable isotopically labelled derivative of the glucosinolate glucoraphanin, namely [10- 13 C,11,12- 2 H 5 ]glucoraphanin, is described. This also represents the first total chemical synthesis of glucoraphanin itself.
John Morrison, Nigel P Botting
exaly +3 more sources

