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Medchemexpress LLC Z-L(D-Val)G-CHN2 | 00-00-0 | 99.4% | 445.51 g·mol⁻¹ | C22H31N5O5 | 5 MG
SDP

Catalog No. 5000243035
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Z-L(D-Val)G-CHN2 is a tripeptide-derived, cell-permeable, irreversible inhibitor of cysteine proteinases that mimics part of the human protease-binding center. It has reported antiviral activity, including inhibition of herpes simplex virus replication and blockade of SARS-CoV-2 3CL protease activity (reported EC50 = 190 nM). Supplied as a high-purity research reagent for in vitro studies.

  • Irreversible inhibition of cysteine proteinases.
  • Tripeptide-derived structure that mimics the protease-binding center.
  • Demonstrated antiviral activity against HSV and SARS-CoV-2 (3CL protease inhibition).
  • High purity (reported 99.35%).
  • Provided in a small laboratory-scale quantity suitable for in vitro work.
  • Molecular weight 445.51 g·mol⁻¹, characterized by analytical data.

Catalog No. 50-002-43035 Supplier Medchemexpress LLC Supplier No. HY108137A5MG
May include imposed supplier surcharges.
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Z-L(D-Val)G-CHN2 is a tripeptide-derived, cell-permeable, irreversible inhibitor of cysteine proteinases that mimics part of the human protease-binding center. It has reported antiviral activity, including inhibition of herpes simplex virus replication and blockade of SARS-CoV-2 3CL protease activity (reported EC50 = 190 nM). Supplied as a high-purity research reagent for in vitro studies.

  • Irreversible inhibition of cysteine proteinases.
  • Tripeptide-derived structure that mimics the protease-binding center.
  • Demonstrated antiviral activity against HSV and SARS-CoV-2 (3CL protease inhibition).
  • High purity (reported 99.35%).
  • Provided in a small laboratory-scale quantity suitable for in vitro work.
  • Molecular weight 445.51 g·mol⁻¹, characterized by analytical data.

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