ligands acting on targets

(+)-SHIN1 ((+)-RZ-2994) is an active (+) enantiomer of SHIN1.In Vitro(+)-SHIN1 ((+)-RZ-2994) is potent against cytosolic SHMT1 with an IC 50 for blocking growth of less than 50 nM and 870 nM in SHMT2 deletion cells and HCT-116 cells, respectively.

(+)-SHIN1 ((+)-RZ-2994) is an active (+) enantiomer of SHIN1.In Vitro(+)-SHIN1 ((+)-RZ-2994) is potent against cytosolic SHMT1 with an IC 50 for blocking growth of less than 50 nM and 870 nM in SHMT2 deletion cells and HCT-116 cells, respectively.

(+)-SHIN1 ((+)-RZ-2994) is an active (+) enantiomer of SHIN1.In Vitro(+)-SHIN1 ((+)-RZ-2994) is potent against cytosolic SHMT1 with an IC 50 for blocking growth of less than 50 nM and 870 nM in SHMT2 deletion cells and HCT-116 cells, respectively.

(+)-SHIN1 ((+)-RZ-2994) is an active (+) enantiomer of SHIN1.In Vitro(+)-SHIN1 ((+)-RZ-2994) is potent against cytosolic SHMT1 with an IC 50 for blocking growth of less than 50 nM and 870 nM in SHMT2 deletion cells and HCT-116 cells, respectively.

(+)-SHIN1 ((+)-RZ-2994) is an active (+) enantiomer of SHIN1.In Vitro(+)-SHIN1 ((+)-RZ-2994) is potent against cytosolic SHMT1 with an IC 50 for blocking growth of less than 50 nM and 870 nM in SHMT2 deletion cells and HCT-116 cells, respectively.

(+)-SJ733.

(+)-SJ733.

(+)-SKF 10.047.

(+)-SKF 10.047.

(+)-Sophoridine acts as an anti-inflammatory agent. It can be studied as a potential anticancer agent, with a promising anti-rumor effect and lower toxicity.

(+)-Sparteine is a natural alkaloid acting as a ganglionic blocking agent. (+)-Sparteine competitively blocks nicotinic ACh receptor in the neurons.

(+)-sparteine (sulfate pentahydrate) is a ganglionic blocking agent. (+)-Sparteine competitively blocks nicotinic ACh receptor in the neurons.Appearance:SolidIC50&amp: Target:nAChRIn Vitro:(+)-Sparteine (2 μM) (sulfate pentahydrate) reduces the