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C358747-5mgProduct Describtion:HG-10-102-01 is a potent and selective inhibitor of wild-type LRRK2 with IC50 of 23.3 nM and the G2019S mutant with IC50 of 3.2 nM.
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H610827-25mgHG-10-102-01.
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H610827-5mgHG-10-102-01.
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H413999-100mgInformationHG-9-91-01 HG-9-91-01 (SIK inhibitor 1) is a potent and highly selective inhibitor of salt-inducible kinase (SIK) with IC50 of 0.92 nM, 6.6 nM and 9.6 nM for SIK1, SIK2 and SIK3, respectively.TargetsSIK1 (Cell-free assay): SIK2 (Cell-free
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H413999-25mgInformationHG-9-91-01 HG-9-91-01 (SIK inhibitor 1) is a potent and highly selective inhibitor of salt-inducible kinase (SIK) with IC50 of 0.92 nM, 6.6 nM and 9.6 nM for SIK1, SIK2 and SIK3, respectively.TargetsSIK1 (Cell-free assay): SIK2 (Cell-free
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H413999-5mgInformationHG-9-91-01 HG-9-91-01 (SIK inhibitor 1) is a potent and highly selective inhibitor of salt-inducible kinase (SIK) with IC50 of 0.92 nM, 6.6 nM and 9.6 nM for SIK1, SIK2 and SIK3, respectively.TargetsSIK1 (Cell-free assay): SIK2 (Cell-free
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H610835-25mgHis-Leu-lopinavir.
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H610835-5mgHis-Leu-lopinavir.
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H610840-25mghistaprodifen.
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H288693-100mgSelective Epac2 inhibitor.
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H288693-10mgSelective Epac2 inhibitor.