Levonorgestrelis a synthetic progesterone analog; binds to the progesterone receptor (relative binding affinities are < 0.02, 7.5, 17, 58 and 323 % for estrogen receptors, glucocorticoid receptors, mineralocorticoid receptors, androgen receptors and progesterone receptors respectively).
More Information Supplier PageCalcium Folinate, Pentahydrate supplies cells with tetrahydrofolate and diminishes methotrexate toxicity without abolishing antitumor effect.
More Information Supplier PageCalcium Folinate, Pentahydrate supplies cells with tetrahydrofolate and diminishes methotrexate toxicity without abolishing antitumor effect.
More Information Supplier PageLBH589 is a hydroxamic acid and acts as a non-selective HDAC inhibitor with IC5o of HDAC1 to be 0.23 nM.
More Information Supplier PageLBH589 is a hydroxamic acid and acts as a non-selective HDAC inhibitor with IC5o of HDAC1 to be 0.23 nM.
More Information Supplier PageL-Ascorbyl 6-palmitate (Ascorbyl palmitate) is an ester formed from ascorbic acid and palmitic acid creating a fat-soluble form of vitamin C.
More Information Supplier PageL-Ascorbyl 6-palmitate (Ascorbyl palmitate) is an ester formed from ascorbic acid and palmitic acid creating a fat-soluble form of vitamin C.
More Information Supplier PageL-Ascorbyl 6-palmitate (Ascorbyl palmitate) is an ester formed from ascorbic acid and palmitic acid creating a fat-soluble form of vitamin C.
More Information Supplier PageL-Ascorbyl 6-palmitate (Ascorbyl palmitate) is an ester formed from ascorbic acid and palmitic acid creating a fat-soluble form of vitamin C.
More Information Supplier PageLAQ824 (NVP-LAQ824) is a potent novel histone deacetylase inhibitor with significant activity against multiple myeloma.
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