Activin and Inhibin

BSH-IN-1 is a potent and covalent inhibitor of gut bacterial recombinant bile salt hydrolases ( BSH s) with IC 50 s of 108 nM and 427 nM for B. longum BSH (Gram positive) and B. theta BSH (Gram negative), respectively.In VitroBSH-IN-1 (Compound 7)

BSH-IN-1 is a potent and covalent inhibitor of gut bacterial recombinant bile salt hydrolases ( BSH s) with IC 50 s of 108 nM and 427 nM for B. longum BSH (Gram positive) and B. theta BSH (Gram negative), respectively.In VitroBSH-IN-1 (Compound 7)

BSH-IN-1 is a potent and covalent inhibitor of gut bacterial recombinant bile salt hydrolases ( BSH s) with IC 50 s of 108 nM and 427 nM for B. longum BSH (Gram positive) and B. theta BSH (Gram negative), respectively.In VitroBSH-IN-1 (Compound 7)

BSH-IN-1 is a potent and covalent inhibitor of gut bacterial recombinant bile salt hydrolases ( BSH s) with IC 50 s of 108 nM and 427 nM for B. longum BSH (Gram positive) and B. theta BSH (Gram negative), respectively.In VitroBSH-IN-1 (Compound 7)

BSJ-04-122 is a covalent MKK4/7 dual inhibitor. BSJ-04-122 inhibits MKK4 and MKK7 with IC 50 values of 4 nM and 181 nM, respectively. BSJ-04-122 can be used for the research of cancerIn VitroBSJ-04-122 has inhibitory activity for MKK4 and MKK7 with

BSJ-04-122 is a covalent MKK4/7 dual inhibitor. BSJ-04-122 inhibits MKK4 and MKK7 with IC 50 values of 4 nM and 181 nM, respectively. BSJ-04-122 can be used for the research of cancerIn VitroBSJ-04-122 has inhibitory activity for MKK4 and MKK7 with

BSJ-04-122 is a covalent MKK4/7 dual inhibitor. BSJ-04-122 inhibits MKK4 and MKK7 with IC 50 values of 4 nM and 181 nM, respectively. BSJ-04-122 can be used for the research of cancerIn VitroBSJ-04-122 has inhibitory activity for MKK4 and MKK7 with

BSJ-04-122 is a covalent MKK4/7 dual inhibitor. BSJ-04-122 inhibits MKK4 and MKK7 with IC 50 values of 4 nM and 181 nM, respectively. BSJ-04-122 can be used for the research of cancerIn VitroBSJ-04-122 has inhibitory activity for MKK4 and MKK7 with

BSJ-04-122 is a covalent MKK4/7 dual inhibitor. BSJ-04-122 inhibits MKK4 and MKK7 with IC 50 values of 4 nM and 181 nM, respectively. BSJ-04-122 can be used for the research of cancerIn VitroBSJ-04-122 has inhibitory activity for MKK4 and MKK7 with

Budesonide impurity C is an impurity of Budesonide. Budesonide, an inhaled glucocortical steroid, is an orally active glucocorticoid receptor agonist.In VitroBudesonide is selective for human glucocorticoid receptor (hGR: EC 50 =45.7 pM) over

Budesonide impurity C is an impurity of Budesonide. Budesonide, an inhaled glucocortical steroid, is an orally active glucocorticoid receptor agonist.In VitroBudesonide is selective for human glucocorticoid receptor (hGR: EC 50 =45.7 pM) over

Bufuralol (Ro 3-4787) hydrochloride is a potent non-selective, orally active β-adrenoreceptor antagonist with partial agonist activity. Bufuralol hydrochloride is a CYP2D6 probe substrateIn VitroBufuralol (Ro 3-4787) hydrochloride is widely used in