| Cat.No. | Name | Information |
|---|---|---|
| M53384 | Ac-VRPR-AMC | Ac-VRPR-AMC is a fluorogenic metacaspase substrate. |
| M53383 | Ac-YVAD-AOM | Ac-YVAD-AOM is the inhibitor of caspase-1 that shows antitumor activity. |
| M53382 | Ac-VAD-CHO | Ac-VAD-CHO (Ac-Val-Ala-Asp-CHO) is a pan-caspase inhibitor. |
| M53381 | Ac-VAD-pNA | Ac-VAD-pNA is a caspase-1 substrate. |
| M53380 | Z-IETD-pNA | Z-IETD-pNA (Z-Ile-Glu-Thr-Asp-pNA) is a colorimetric caspase-8 and granzyme B substrate. |
| M53379 | Z-VEID-AFC | Z-VEID-AFC is a fluorescent substrate for caspase-6. |
| M53378 | Z-YVAD-CMK | Z-YVAD-CMK is a caspase-1 and caspase-3 inhibitor. |
| M53377 | Z-YVAD-pNA | Z-YVAD-pNA (Z-Tyr-Val-Ala-Asp-pNA) is a caspase-1 substrate. |
| M53376 | Z-VAD-AMC | Z-VAD-AMC is a substrate of caspase-9. |
| M53375 | TRP-601 | TRP-601 is a caspase inhibitor. |
| M53374 | GPR | GPR is a three amino acid peptide. |
| M53373 | PRDX3(103-112) SO3 modified, human | PRDX3(103-112) SO3 modified, human is a marker of ferroptosis, and can be used for liver diseases study. |
| M53372 | PRDX3(103-112), human | PRDX3(103-112), human is a marker for ferroptosis. |
| M53371 | p53 (17-26) | p53 (17-26) is amino acids 17 to 26 fragment of p53. |
| M53370 | Azurin p28 peptide | Azurin p28 peptide is a tumor-penetrated antitumor peptide. |
| M53369 | RIPK1-IN-12 | RIPK1-IN-12 is a potent RIPK1 inhibitor. |
| M53368 | N, O-Didansyl-L-tyrosine cyclohexylammonium | N,O-Didansyl-L-tyrosine cyclohexylammonium is a potent selective thymidylate synthase (TS) inhibitor, acts on TS of Escherichia coli, Lactobacillus casei and human with the IC50 values of 5.0, 3.4 and 119 μM, respectively. |
| M53367 | LEESGGGLVQPGGSMK | LEESGGGLVQPGGSMK, a proteolysis peptide, is a component of Infliximab. |
| M53366 | Delmitide | Delmitide (RDP58) is an orally active d-isomer decapeptide with potent anti-inflammatory activity. |
| M53364 | Calmodulin-Dependent Protein Kinase II (290-309) | Calmodulin-Dependent Protein Kinase II (290-309) is a potent CaMK antagonist with an IC50 of 52 nM for inhibition of Ca2+/calmodulin-dependent protein kinase II. |
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