Biologically Active Small Molecules

An inhibitor of the initiation of translation that blocks the interaction of eIF4G with eIF4E (KD = 25 &muM) prevents the expression of oncogenic proteins in mammalian cancer cells, leading to apoptosis blocks translation in some viruses that do

An inhibitor of the initiation of translation that blocks the interaction of eIF4G with eIF4E (KD = 25 &muM) prevents the expression of oncogenic proteins in mammalian cancer cells, leading to apoptosis blocks translation in some viruses that do

An inhibitor of the initiation of translation that blocks the interaction of eIF4G with eIF4E (KD = 25 &muM) prevents the expression of oncogenic proteins in mammalian cancer cells, leading to apoptosis blocks translation in some viruses that do

An inhibitor of the initiation of translation that blocks the interaction of eIF4G with eIF4E (KD = 25 &muM) prevents the expression of oncogenic proteins in mammalian cancer cells, leading to apoptosis blocks translation in some viruses that do

A specific adenosine A2 receptor agonist with antipyretic and anticonvulsant activity stimulates the production of cyclic AMP in CHO-K1 cells with an EC₅₀ value of 5.3 &microM.

A specific adenosine A2 receptor agonist with antipyretic and anticonvulsant activity stimulates the production of cyclic AMP in CHO-K1 cells with an EC₅₀ value of 5.3 &microM.

A specific adenosine A2 receptor agonist with antipyretic and anticonvulsant activity stimulates the production of cyclic AMP in CHO-K1 cells with an EC₅₀ value of 5.3 &microM.

An intermediate in the generation of adenine and methionine that is produced by the decarboxylation of SAM a potent agonist of adenosine receptors (Kis = 0.15, 1.

An intermediate in the generation of adenine and methionine that is produced by the decarboxylation of SAM a potent agonist of adenosine receptors (Kis = 0.15, 1.

An intermediate in the generation of adenine and methionine that is produced by the decarboxylation of SAM a potent agonist of adenosine receptors (Kis = 0.15, 1.

A form of thymidine in which the hydroxyl group on carbon 5 of ribose has been replaced with hydrogen and cannot be phosphorylated competitively inhibits the cellular influx of thymidine.

A form of thymidine in which the hydroxyl group on carbon 5 of ribose has been replaced with hydrogen and cannot be phosphorylated competitively inhibits the cellular influx of thymidine.