Rituximab

Risarestat (CT-112), an aldose reductase inhibitor, is developed for the treatment of diabetic complications.In VivoRisarestat inhibits the accumulation of dulcitol in a dose-dependent manner, except for the 1.0% solution which has an activity

Ritonavir-d 6 is the deuterium labeled Ritonavir. Ritonavir (ABT 538) is an inhibitor of HIV protease used to treat HIV infection and AIDS. Ritonavir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 1.61 μM.In VitroStable heavy isotopes of

InformationTenalisib (RP6530) is a potent and selective dualPI3Kδ/γinhibitor withIC50values of 24.5 nM and 33.2 nM for PI3Kδ and PI3Kγ, respectively. Its selectivity over α and β isoforms are more than 300-fold and 100-fold,

InformationTenalisib (RP6530) is a potent and selective dualPI3Kδ/γinhibitor withIC50values of 24.5 nM and 33.2 nM for PI3Kδ and PI3Kγ, respectively. Its selectivity over α and β isoforms are more than 300-fold and 100-fold,

InformationTenalisib (RP6530) is a potent and selective dualPI3Kδ/γinhibitor withIC50values of 24.5 nM and 33.2 nM for PI3Kδ and PI3Kγ, respectively. Its selectivity over α and β isoforms are more than 300-fold and 100-fold,

InformationTenalisib (RP6530) is a potent and selective dualPI3Kδ/γinhibitor withIC50values of 24.5 nM and 33.2 nM for PI3Kδ and PI3Kγ, respectively. Its selectivity over α and β isoforms are more than 300-fold and 100-fold,

InformationTenalisib (RP6530) is a potent and selective dualPI3Kδ/γinhibitor withIC50values of 24.5 nM and 33.2 nM for PI3Kδ and PI3Kγ, respectively. Its selectivity over α and β isoforms are more than 300-fold and 100-fold,

InformationTenalisib (RP6530) is a potent and selective dualPI3Kδ/γinhibitor withIC50values of 24.5 nM and 33.2 nM for PI3Kδ and PI3Kγ, respectively. Its selectivity over α and β isoforms are more than 300-fold and 100-fold,

Trans-Chalcone is an open chain flavonoid that inhibits lung and forestomach carcinogenesis.

Trans-Chalcone is an open chain flavonoid that inhibits lung and forestomach carcinogenesis.

Trans-Chalcone is an open chain flavonoid that inhibits lung and forestomach carcinogenesis.

Trans-Chalcone is an open chain flavonoid that inhibits lung and forestomach carcinogenesis.