Activin and Inhibin

(S)-Carvedilol, the S-enantiomer of Carvedilol, is a non-selective β/α-1 blocker. (S)-Carvedilol exerts protection against the vascular or cardiac toxicity of Doxorubicin (DOX)In VitroThe β-receptor blocking activity of (S)-Carvedilol is about 100

(S)-Ceralasertib ((S)-AZD6738) is extracted from patent WO2011154737A1, Compound II, exhibits an IC 50 of 2.578 nM.(S)-Ceralasertib is a potent and selective sulfoximine morpholinopyrimidine ATR inhibitor with excellent preclinical physicochemical

(S)-Ceralasertib ((S)-AZD6738) is extracted from patent WO2011154737A1, Compound II, exhibits an IC 50 of 2.578 nM.(S)-Ceralasertib is a potent and selective sulfoximine morpholinopyrimidine ATR inhibitor with excellent preclinical physicochemical

(S)-Ceralasertib ((S)-AZD6738) is extracted from patent WO2011154737A1, Compound II, exhibits an IC 50 of 2.578 nM.(S)-Ceralasertib is a potent and selective sulfoximine morpholinopyrimidine ATR inhibitor with excellent preclinical physicochemical

(S)-Ceralasertib ((S)-AZD6738) is extracted from patent WO2011154737A1, Compound II, exhibits an IC 50 of 2.578 nM.(S)-Ceralasertib is a potent and selective sulfoximine morpholinopyrimidine ATR inhibitor with excellent preclinical physicochemical

(S)-Ceralasertib ((S)-AZD6738) is extracted from patent WO2011154737A1, Compound II, exhibits an IC 50 of 2.578 nM.(S)-Ceralasertib is a potent and selective sulfoximine morpholinopyrimidine ATR inhibitor with excellent preclinical physicochemical

(S)-Dolaphenine hydrochloride is a component of Dolastatin 10 ( HY-15580 ). Dolastatin 10, an antineoplastic agent, inhibits tubulin polymerization.Form:Solid.

(S)-Dolaphenine hydrochloride is a component of Dolastatin 10 ( HY-15580 ). Dolastatin 10, an antineoplastic agent, inhibits tubulin polymerization.Form:Solid.

(S)-Dolaphenine hydrochloride is a component of Dolastatin 10 ( HY-15580 ). Dolastatin 10, an antineoplastic agent, inhibits tubulin polymerization.

FTY720 (S)-Phosphate is an agonist of S1P receptor 1 (S1PR1) , used in the research of acute inflammatory diseases such as acute lung injury.In VitroFTY720 (S)-Phosphate is an agonist of S1PR1. FTY720 (S)-Phosphate (Tys, 1 μM) maintains S1PR1

FTY720 (S)-Phosphate is an agonist of S1P receptor 1 (S1PR1) , used in the research of acute inflammatory diseases such as acute lung injury.In VitroFTY720 (S)-Phosphate is an agonist of S1PR1. FTY720 (S)-Phosphate (Tys, 1 μM) maintains S1PR1

(S)-GFB-12811 (compound 596) is a potent and selective CDK5 inhibitor, with an IC 50 value less than 10 nM. (S)-GFB-12811 can be used in the research of cell cycle progression, neuronal development, tumorigenesisForm:SolidIC50&amp: Target:CDK5