A reduced form of folic acid that serves as a cofactor in methyltransferase reactions and is the major one-carbon carrier in one carbon metabolism important for the synthesis of thymidine for incorporation into DNA or the synthesis of purines, as
A reduced form of folic acid that serves as a cofactor in methyltransferase reactions and is the major one-carbon carrier in one carbon metabolism important for the synthesis of thymidine for incorporation into DNA or the synthesis of purines, as
A fibrate that acts as a lipid-lowering agent, decreasing low-density lipoprotein cholesterol and triglycerides displays high affinity for L-FABP (K<sub>i</sub> = 24 nM) exhibits EC<sub>50</sub> values of 18 and 30 µM for murine and human
A fibrate that acts as a lipid-lowering agent, decreasing low-density lipoprotein cholesterol and triglycerides displays high affinity for L-FABP (K<sub>i</sub> = 24 nM) exhibits EC<sub>50</sub> values of 18 and 30 µM for murine and human
An antioxidant and free radical scavenging compound extracted from S. miltiorrhiza that has been investigated for its cardioprotective and chemopreventative properties.
An antioxidant and free radical scavenging compound extracted from S. miltiorrhiza that has been investigated for its cardioprotective and chemopreventative properties.
Traumatic acid is a product of the hydroperoxide lyase pathway in plants. It is a wound healing agent that stimulates cell division near a wound site to form a protective callus.
Traumatic acid is a product of the hydroperoxide lyase pathway in plants. It is a wound healing agent that stimulates cell division near a wound site to form a protective callus.
An antioxidant and free radical scavenging compound extracted from S. miltiorrhiza that has been investigated for its cardioprotective and chemopreventative properties.
An antioxidant and free radical scavenging compound extracted from S. miltiorrhiza that has been investigated for its cardioprotective and chemopreventative properties.
An inhibitor of USP14 and UCHL5, two proteasome-associated deubiquitinases inhibits DUB activity in purified 19S proteasomes with an IC50 value of 2.1 µM blocks tumor progression in vivo in mice and prevents organ infiltration in mouse
An inhibitor of USP14 and UCHL5, two proteasome-associated deubiquitinases inhibits DUB activity in purified 19S proteasomes with an IC50 value of 2.1 µM blocks tumor progression in vivo in mice and prevents organ infiltration in mouse
A ribonucleotide reductase inhibitor and iron chelator with antitumor activity inhibits DNA synthesis and repair by destroying the tyrosine free radical in the R2/p53R2 subunits of ribonucleotide reductase through the formation of a redox active
A ribonucleotide reductase inhibitor and iron chelator with antitumor activity inhibits DNA synthesis and repair by destroying the tyrosine free radical in the R2/p53R2 subunits of ribonucleotide reductase through the formation of a redox active
A natural indole alkaloid with demonstrated beneficial effects in cancer, obesity, inflammation, and many other conditions an AhR antagonist (Ki = 28 nM), activator of TRPV1 (EC<sub>50</sub> = 45 nM), and inhibitor of signaling through NF-&kappaB.
A natural indole alkaloid with demonstrated beneficial effects in cancer, obesity, inflammation, and many other conditions an AhR antagonist (Ki = 28 nM), activator of TRPV1 (EC<sub>50</sub> = 45 nM), and inhibitor of signaling through NF-&kappaB.
A natural triterpene that has diverse anti-inflammatory and anti-diabetic effects, blocking NF-&kappaB activation in macrophages and altering lipid metabolism in mice, at least in part through antioxidant actions.
A natural triterpene that has diverse anti-inflammatory and anti-diabetic effects, blocking NF-&kappaB activation in macrophages and altering lipid metabolism in mice, at least in part through antioxidant actions.