AZD7545 10mg | ≥99%
CSNpharm
AZD7545 is a selective inhibitor of PDHK2 (PDH kinase2) with IC50s of 36.8 nM and 6.4 nM for PDHK1 and PDHK2 respectively.
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AZD7545 is a selective inhibitor of PDHK2 (PDH kinase2) with IC50s of 36.8 nM and 6.4 nM for PDHK1 and PDHK2 respectively.
More Information Supplier Page
AZD7545 is a selective inhibitor of PDHK2 (PDH kinase2) with IC50s of 36.8 nM and 6.4 nM for PDHK1 and PDHK2 respectively.
More Information Supplier Page
AZD7545 is a selective inhibitor of PDHK2 (PDH kinase2) with IC50s of 36.8 nM and 6.4 nM for PDHK1 and PDHK2 respectively.
More Information Supplier Page
AZD7545 is a selective inhibitor of PDHK2 (PDH kinase2) with IC50s of 36.8 nM and 6.4 nM for PDHK1 and PDHK2 respectively.
More Information Supplier Page
AZD7545 is a selective inhibitor of PDHK2 (PDH kinase2) with IC50s of 36.8 nM and 6.4 nM for PDHK1 and PDHK2 respectively.
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D4476 is a potent, selective, and cell-permeant CK1 (casein kinase 1) inhibitor with IC50 of 200 nM and 300 nM in a cell-free assay for CK1 from Schizosaccharomyces pombe and CK1δ, respectively. Also acts as an ALK5 inhibitor with IC50 of 500 nM.
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D4476 is a potent, selective, and cell-permeant CK1 (casein kinase 1) inhibitor with IC50 of 200 nM and 300 nM in a cell-free assay for CK1 from Schizosaccharomyces pombe and CK1δ, respectively. Also acts as an ALK5 inhibitor with IC50 of 500 nM.
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D4476 is a potent, selective, and cell-permeant CK1 (casein kinase 1) inhibitor with IC50 of 200 nM and 300 nM in a cell-free assay for CK1 from Schizosaccharomyces pombe and CK1δ, respectively. Also acts as an ALK5 inhibitor with IC50 of 500 nM.
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D4476 is a potent, selective, and cell-permeant CK1 (casein kinase 1) inhibitor with IC50 of 200 nM and 300 nM in a cell-free assay for CK1 from Schizosaccharomyces pombe and CK1δ, respectively. Also acts as an ALK5 inhibitor with IC50 of 500 nM.
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Mirabegron is an agonist of β3 adrenergic receptor with EC50 value of 22.4nM, used for the treatment of overactive bladder.
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