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S651208-5mg(R)-Selisistat ((R)-EX-527) is a R-enantiomer of Selisistat. Selisistat (EX-527) is a potent and selective SIRT1 inhibitor with IC 50 of 98 nM.Form:SolidIC50&: Target:IC50: >: 100 μM (SIRT1).
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S656580-1ml(R)-Selisistat ((R)-EX-527) is a R-enantiomer of Selisistat. Selisistat (EX-527) is a potent and selective SIRT1 inhibitor with IC 50 of 98 nM.IC50&: Target:IC50: >: 100 μM (SIRT1).
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T650138-100mg(R)-Tegoprazan (example 3), a benzimidazole derivative, is a potent kidney H + /K + -ATPase inhibitor with an IC 50 of 98 nM of canine kidney Na + /K + -ATPase. (R)-Tegoprazan has the potential for gastrointestinal diseases research.Form:Solid.
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T650138-10mg(R)-Tegoprazan (example 3), a benzimidazole derivative, is a potent kidney H + /K + -ATPase inhibitor with an IC 50 of 98 nM of canine kidney Na + /K + -ATPase. (R)-Tegoprazan has the potential for gastrointestinal diseases research.Form:Solid.
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T650138-25mg(R)-Tegoprazan (example 3), a benzimidazole derivative, is a potent kidney H + /K + -ATPase inhibitor with an IC 50 of 98 nM of canine kidney Na + /K + -ATPase. (R)-Tegoprazan has the potential for gastrointestinal diseases research.Form:Solid.
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T650138-50mg(R)-Tegoprazan (example 3), a benzimidazole derivative, is a potent kidney H + /K + -ATPase inhibitor with an IC 50 of 98 nM of canine kidney Na + /K + -ATPase. (R)-Tegoprazan has the potential for gastrointestinal diseases research.Form:Solid.
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T650138-5mg(R)-Tegoprazan (example 3), a benzimidazole derivative, is a potent kidney H + /K + -ATPase inhibitor with an IC 50 of 98 nM of canine kidney Na + /K + -ATPase. (R)-Tegoprazan has the potential for gastrointestinal diseases research.Form:Solid.
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T646849-10mg(R)-Terazosin is an active R-enantiomer of Terazosin. (R)-Terazosin is a potent α1-adrenoceptor antagonist with K i values of 6.51 nM, 1.01 nM and 1.97 nM for α1a , α1b and α1d-adrenoceptor , respectivelyIn Vitro(R)-Terazosin is low affinity for
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T646849-50mg(R)-Terazosin is an active R-enantiomer of Terazosin. (R)-Terazosin is a potent α1-adrenoceptor antagonist with K i values of 6.51 nM, 1.01 nM and 1.97 nM for α1a , α1b and α1d-adrenoceptor , respectivelyIn Vitro(R)-Terazosin is low affinity for
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T646849-5mg(R)-Terazosin is an active R-enantiomer of Terazosin. (R)-Terazosin is a potent α1-adrenoceptor antagonist with K i values of 6.51 nM, 1.01 nM and 1.97 nM for α1a , α1b and α1d-adrenoceptor , respectivelyIn Vitro(R)-Terazosin is low affinity for
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T654769-1ml(R)-Terazosin is an active R-enantiomer of Terazosin. (R)-Terazosin is a potent α1-adrenoceptor antagonist with K i values of 6.51 nM, 1.01 nM and 1.97 nM for α1a , α1b and α1d-adrenoceptor , respectivelyIn Vitro(R)-Terazosin is low affinity for
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U647495-100mg(R)-UT-155 (compound 11) is a selective androgen receptor degrader (SARD) ligand. Less active than the S-isomer.Form:Solid.