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mp-2

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    112
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Myelopeptide-2 (MP-2)
TP2193
Myelopeptide-2 (MP-2) with the sequence Leu-Val-Val-Tyr-Pro-Trp is originally isolated from the supernatant of porcine bone marrow cell culture and is able to restore the mitogen responsiveness of human T lymphocytes inhibited by conditioned medium from H
  • $115
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GPLGIAGQ acetate
GPLGIAGQ acetate(109053-09-0 Free base)
TP1535L
GPLGIAGQ acetate is a MMP2-cleavable polypeptide. GPLGIAGQ acetate can be used as a stimulus-sensitive linker in both liposomal and micellar nanocarriers to synthesis unique MMP2-targeted photosensitizer in photodynamic therapy.
  • $30
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Histatin 5 acetate
Histatin 5 acetate (115966-68-2 Free base)
TP1741L
Histatin 5 acetate inhibits the activity of the host matrix metalloproteinases MMP-2 and MMP-9 with IC50s of 0.57 and 0.25 μM, respectively.
  • $75
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Proadrenomedullin (N-20) (bovine, porcine)
ProADM N20(bovine, porcine), PAMP-20(bovine, porcine)
T80503
Proadrenomedullin (N-20) (ProADM N20) (bovine, porcine) is a peptide known for its strong hypotensive effects and inhibition of catecholamine release from chromaffin cells. It effectively suppresses catecholamine secretion in PC12 pheochromocytoma cells with an IC50 of 350 nM and prevents the desensitization of nicotinic cholinergic agonist-induced catecholamine release and nicotinic signal transduction, with an EC50 of approximately 270 nM for desensitization blockade, as evidenced by inhibited 22 Na+ uptake [1].
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BMP2-derived peptide
T82851836606-84-9
BMP2-derived peptide, encompassing amino acids 73 to 92 of BMP-2, induces osteogenic differentiation in bone marrow stromal cells (BMSCs) and augments bone regeneration [1].
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Histatin 5 (TFA)(115966-68-2,free)
Histatin 5 (TFA)
TP1446
Histatin 5 (TFA)(115966-68-2,free) (Histatin 5 (TFA)) inhibits the activity of the host matrix metalloproteinases MMP-2 and MMP-9 with IC50s of 0.57 and 0.25 μM, respectively.
  • $171
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Mp-4D7-pF2
TP3890
Mp-4D7-pF2 is a cell-penetrating bicycle peptide that acts as a non-covalent inhibitor of the SARS-CoV-2 main protease (SARS-CoV-2 main protease) with an IC50 of 4.51 μM. It exhibits antiviral activity against SARS-CoV-2 without cytotoxicity and can be utilized in COVID-19 infection research.
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