Biologically Active Small Molecules

A prominent member of a class of reactive LO-catalyzed peroxidative decomposition products of unsaturated fatty acids that are formed when diatoms are crushed or eaten.

A prominent member of a class of reactive LO-catalyzed peroxidative decomposition products of unsaturated fatty acids that are formed when diatoms are crushed or eaten.

A prominent member of a class of reactive LO-catalyzed peroxidative decomposition products of unsaturated fatty acids that are formed when diatoms are crushed or eaten.

A mechanism-based, irreversible inhibitor of CYP4A2, an enzyme that predominantly synthesizes 20-HETE in the mammalian kidney.

A mechanism-based, irreversible inhibitor of CYP4A2, an enzyme that predominantly synthesizes 20-HETE in the mammalian kidney.

A mechanism-based, irreversible inhibitor of CYP4A2, an enzyme that predominantly synthesizes 20-HETE in the mammalian kidney.

A selective DDR1 inhibitor (IC₅₀ = 105 nM EC₅₀ = 87 nM inhibits colorectal cancer cell lines when used in combination with the PI3K/mTOR inhibitor, GSK2126458.

A selective DDR1 inhibitor (IC₅₀ = 105 nM EC₅₀ = 87 nM inhibits colorectal cancer cell lines when used in combination with the PI3K/mTOR inhibitor, GSK2126458.

A selective DDR1 inhibitor (IC₅₀ = 105 nM EC₅₀ = 87 nM inhibits colorectal cancer cell lines when used in combination with the PI3K/mTOR inhibitor, GSK2126458.

A NO donor with a half-life of 2 minutes at 37&degC, pH 7.4 liberates 1.5 moles of NO per mole of parent compound.

A NO donor with a half-life of 2 minutes at 37&degC, pH 7.4 liberates 1.5 moles of NO per mole of parent compound.

A NO donor with a half-life of 2 minutes at 37&degC, pH 7.4 liberates 1.5 moles of NO per mole of parent compound.