Guanazodine sulfate monohydrate

InformationTalatisamine, a delphinine type alkaloid extracted from Aconitum talassicum, is a newly identified K+ channel blocker with hypotensive and antiarrhythmic activities.TargetsIK channel 146 μMIn vitroTalatisamine is a specific blocker for IK

InformationTalatisamine, a delphinine type alkaloid extracted from Aconitum talassicum, is a newly identified K+ channel blocker with hypotensive and antiarrhythmic activities.TargetsIK channel 146 μMIn vitroTalatisamine is a specific blocker for IK

InformationTalatisamine, a delphinine type alkaloid extracted from Aconitum talassicum, is a newly identified K+ channel blocker with hypotensive and antiarrhythmic activities.TargetsIK channel 146 μMIn vitroTalatisamine is a specific blocker for IK

InformationTalatisamine, a delphinine type alkaloid extracted from Aconitum talassicum, is a newly identified K+ channel blocker with hypotensive and antiarrhythmic activities.TargetsIK channel 146 μMIn vitroTalatisamine is a specific blocker for IK

InformationTalatisamine, a delphinine type alkaloid extracted from Aconitum talassicum, is a newly identified K+ channel blocker with hypotensive and antiarrhythmic activities.TargetsIK channel 146 μMIn vitroTalatisamine is a specific blocker for IK

Product Application:Tributyl(1-propynyl)tin can be used:As a starting material in the synthesis of phenyl-substituted pyrimidine-dione by reacting with ethyl isocyanate via cycloaddition and Stille coupling reactions.In the synthesis of 18F labeled

Product Application:Tributyl(1-propynyl)tin can be used:As a starting material in the synthesis of phenyl-substituted pyrimidine-dione by reacting with ethyl isocyanate via cycloaddition and Stille coupling reactions.In the synthesis of 18F labeled

Product Application:Tributyl(1-propynyl)tin can be used:As a starting material in the synthesis of phenyl-substituted pyrimidine-dione by reacting with ethyl isocyanate via cycloaddition and Stille coupling reactions.In the synthesis of 18F labeled

WYE-687 is an ATP-competitive and selective inhibitor of mTOR with IC50 of 7 nM: blocks mTORC1/pS6K(T389) and mTORC2/P-AKT(S473) but no effect observed on P-AKT(T308). Selectivity for mTOR is greater than PI3Kα (&gt:100-fold) and PI3Kγ

WYE-687 is an ATP-competitive and selective inhibitor of mTOR with IC50 of 7 nM: blocks mTORC1/pS6K(T389) and mTORC2/P-AKT(S473) but no effect observed on P-AKT(T308). Selectivity for mTOR is greater than PI3Kα (&gt:100-fold) and PI3Kγ

WYE-687 is an ATP-competitive and selective inhibitor of mTOR with IC50 of 7 nM: blocks mTORC1/pS6K(T389) and mTORC2/P-AKT(S473) but no effect observed on P-AKT(T308). Selectivity for mTOR is greater than PI3Kα (&gt:100-fold) and PI3Kγ

WYE-687 is an ATP-competitive and selective inhibitor of mTOR with IC50 of 7 nM: blocks mTORC1/pS6K(T389) and mTORC2/P-AKT(S473) but no effect observed on P-AKT(T308). Selectivity for mTOR is greater than PI3Kα (&gt:100-fold) and PI3Kγ