Matrix metalloproteinase 7 (MMP-7) is a member of the MMP superfamily and is able to degrade extracellular matrix proteins such as casein, gelatin, fibronectin and proteoglycan. MMP-7 is a validated target for the development of small molecule drugs against cancer. MMP-13 is within the enzyme class the most efficient contributor to type II collagen degeneration and is a validated target in arthritis and cancer. We have developed the dual MMP-7/-13 inhibitor ZHAWOC6941 with IC50-values of 2.2 μM (MMP-7) and 1.2 μM (MMP-13) that is selective over a broad range of MMP isoforms. It spares MMP-1, -2, -3, -8, -9, -12 and -14, making it a valuable modulator for targeted polypharmacology approaches
Collagen degradation and proMMP-2 activation are major functions of MT1-MMP to promote cancer cell i...
Matrix metalloproteinase-13 (MMP-13) is a key enzyme implicated in the degradation of the extracellu...
Matrix metalloproteinases (MMPs) are zinc enzymes responsible for the degradation of the extracellul...
Matrix metalloproteinase 7 (MMP-7) is a member of the MMP superfamily and is able to degrade extrace...
Matrix metalloproteinase 7 (MMP-7) is a member of the MMP superfamily and is able to degrade extrace...
Matrix metalloproteinases (MMPs) play a key role in many diseases like cancer, atherosclerosis or ar...
The matrix metalloproteinase enzyme MMP-13 plays a key role in the degradation of type II collagen i...
Matrix metalloproteinase-7 (MMP-7) has emerged as a protein playing important roles in both physiolo...
Matrix Metalloproteinases (MMPs) are a family of enzymes that are attracting growing interest as the...
MMPs are a group of metalloendopeptidases whose major role is in extracellular matrix (ECM) cataboli...
Osteoarthritis (OA) is the leading cause of joint pain and disability in middle-aged and elderly pat...
Osteoarthritis (OA) is the leading cause of joint pain and disability in middle-aged and elderly pat...
Matrix Metalloproteinases (MMPs) are multidomain zinc endopeptidases which play a central role in de...
The matrix metalloproteinases (MMPs) and their endogenous regulators, the tissue inhibitors of MMPs ...
MMP-13 (collagenase 3), a member of the matrix metalloproteinase family of zinc dependent enzymes, ...
Collagen degradation and proMMP-2 activation are major functions of MT1-MMP to promote cancer cell i...
Matrix metalloproteinase-13 (MMP-13) is a key enzyme implicated in the degradation of the extracellu...
Matrix metalloproteinases (MMPs) are zinc enzymes responsible for the degradation of the extracellul...
Matrix metalloproteinase 7 (MMP-7) is a member of the MMP superfamily and is able to degrade extrace...
Matrix metalloproteinase 7 (MMP-7) is a member of the MMP superfamily and is able to degrade extrace...
Matrix metalloproteinases (MMPs) play a key role in many diseases like cancer, atherosclerosis or ar...
The matrix metalloproteinase enzyme MMP-13 plays a key role in the degradation of type II collagen i...
Matrix metalloproteinase-7 (MMP-7) has emerged as a protein playing important roles in both physiolo...
Matrix Metalloproteinases (MMPs) are a family of enzymes that are attracting growing interest as the...
MMPs are a group of metalloendopeptidases whose major role is in extracellular matrix (ECM) cataboli...
Osteoarthritis (OA) is the leading cause of joint pain and disability in middle-aged and elderly pat...
Osteoarthritis (OA) is the leading cause of joint pain and disability in middle-aged and elderly pat...
Matrix Metalloproteinases (MMPs) are multidomain zinc endopeptidases which play a central role in de...
The matrix metalloproteinases (MMPs) and their endogenous regulators, the tissue inhibitors of MMPs ...
MMP-13 (collagenase 3), a member of the matrix metalloproteinase family of zinc dependent enzymes, ...
Collagen degradation and proMMP-2 activation are major functions of MT1-MMP to promote cancer cell i...
Matrix metalloproteinase-13 (MMP-13) is a key enzyme implicated in the degradation of the extracellu...
Matrix metalloproteinases (MMPs) are zinc enzymes responsible for the degradation of the extracellul...