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Medchemexpress LLC Z-VAD(OMe)-FMK | 187389-52-2 | 98.2% | 467.49 | 50 MG
SDP

Catalog No. 5000391710
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Z-VAD(OMe)-FMK is a cell-permeable and irreversible pan-caspase inhibitor. It is also an ubiquitin carboxy-terminal hydrolase L1 (UCHL1) inhibitor, irreversibly modifying UCHL1 by targeting its active site.

  • Cell-permeable and irreversible pan-caspase inhibitor.
  • Inhibits ubiquitin carboxy-terminal hydrolase L1 (UCHL1).
  • Suppresses caspase-3 activity in lung tissues and decreases the number of terminal dUTP nick-end labeling-positive cells (in vitro).
  • Reduces blood-brain barrier permeability, relieves vasospasm, abolishes brain edema, and improves neurological outcome in subarachnoid hemorrhage (in vitro).
  • Efficiently blocks cell death induced by SMN deficiency (in vitro).
  • Prolongs the survival rate of mice in models of lipopolysaccharide-induced acute lung injury (in vivo).

Catalog No. 50-003-91710 Supplier Medchemexpress LLC Supplier No. HY1665850MG
May include imposed supplier surcharges.
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Z-VAD(OMe)-FMK is a cell-permeable and irreversible pan-caspase inhibitor. It is also an ubiquitin carboxy-terminal hydrolase L1 (UCHL1) inhibitor, irreversibly modifying UCHL1 by targeting its active site.

  • Cell-permeable and irreversible pan-caspase inhibitor.
  • Inhibits ubiquitin carboxy-terminal hydrolase L1 (UCHL1).
  • Suppresses caspase-3 activity in lung tissues and decreases the number of terminal dUTP nick-end labeling-positive cells (in vitro).
  • Reduces blood-brain barrier permeability, relieves vasospasm, abolishes brain edema, and improves neurological outcome in subarachnoid hemorrhage (in vitro).
  • Efficiently blocks cell death induced by SMN deficiency (in vitro).
  • Prolongs the survival rate of mice in models of lipopolysaccharide-induced acute lung injury (in vivo).

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