Activin and Inhibin

GW779439X is a pyrazolopyridazine identified in an inhibitor of the S. aureus PASTA kinase Stk1 . GW779439X potentiates the activity of β-lactam antibiotics against various MRSA and MSSA isolates, some even crossing the breakpoint from resistant to

GW779439X is a pyrazolopyridazine identified in an inhibitor of the S. aureus PASTA kinase Stk1 . GW779439X potentiates the activity of β-lactam antibiotics against various MRSA and MSSA isolates, some even crossing the breakpoint from resistant to

GW779439X is a pyrazolopyridazine identified in an inhibitor of the S. aureus PASTA kinase Stk1 . GW779439X potentiates the activity of β-lactam antibiotics against various MRSA and MSSA isolates, some even crossing the breakpoint from resistant to

GW779439X is a pyrazolopyridazine identified in an inhibitor of the S. aureus PASTA kinase Stk1 . GW779439X potentiates the activity of β-lactam antibiotics against various MRSA and MSSA isolates, some even crossing the breakpoint from resistant to

GW779439X is a pyrazolopyridazine identified in an inhibitor of the S. aureus PASTA kinase Stk1 . GW779439X potentiates the activity of β-lactam antibiotics against various MRSA and MSSA isolates, some even crossing the breakpoint from resistant to

H-Val-Pro-Pro-OH (TFA), a milk-derived proline peptides derivative, is an inhibitor of Angiotensin I converting enzyme (ACE) , with an IC 50 of 9 μM.Appearance:SolidIC50&amp: Target:IC50: 9 μM (ACE) .In Vitro:H-Val-Pro-Pro-OH (TFA), a proline

H-Val-Pro-Pro-OH (TFA), a milk-derived proline peptides derivative, is an inhibitor of Angiotensin I converting enzyme (ACE) , with an IC 50 of 9 μM.Appearance:SolidIC50&amp: Target:IC50: 9 μM (ACE) .In Vitro:H-Val-Pro-Pro-OH (TFA), a proline

H-Val-Pro-Pro-OH (TFA), a milk-derived proline peptides derivative, is an inhibitor of Angiotensin I converting enzyme (ACE) , with an IC 50 of 9 μM.Appearance:SolidIC50&amp: Target:IC50: 9 μM (ACE) .In Vitro:H-Val-Pro-Pro-OH (TFA), a proline

H-Val-Pro-Pro-OH (TFA), a milk-derived proline peptides derivative, is an inhibitor of Angiotensin I converting enzyme (ACE) , with an IC 50 of 9 μM.Appearance:SolidIC50&amp: Target:IC50: 9 μM (ACE) .In Vitro:H-Val-Pro-Pro-OH (TFA), a proline

H3B-6545 is an oral, selective estrogen receptor covalent antagonist ( SERCA ) for the research of metastatic ER-positive, HER2-negative breast cancerIn VitroH3B-6545 is a highly selective small molecule that potently antagonizes wild-type and

H3B-6545 is an oral, selective estrogen receptor covalent antagonist ( SERCA ) for the research of metastatic ER-positive, HER2-negative breast cancerIn VitroH3B-6545 is a highly selective small molecule that potently antagonizes wild-type and

H3B-6545 is an oral, selective estrogen receptor covalent antagonist ( SERCA ) for the research of metastatic ER-positive, HER2-negative breast cancerIn VitroH3B-6545 is a highly selective small molecule that potently antagonizes wild-type and