| Name | (2S)-2-amino-N-[(2S)-2-[[(2S)-4-chloro-3-oxo-1-phenylbutan-2-yl]amino]propanoyl]propanamide |
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| Synonyms |
ALA-ALA-PHE-CMK TFA
H-ALA-ALA-PHE-CMK TFA (L-ALANYL-L-ALANYL-L-PHENYLALANYL)CHLOROMETHANE TRIFLUOROACETATE AAF-CMK TRIFLUOROACETATE AAPCK L-Alaninamide,l-alanyl-N-[(1S)-3-chloro-2-oxo-1-(phenylmethyl)propyl] H-ALA-ALA-PHE-CHLOROMETHYLKETONE TFA TRIPTIDYLPTIDASE II INHIBITOR AAF-CMK TFA H-AAF-CMK, TFA ALA-ALA-PHE-CH2CL TRIFLUOROACETATE Ala-Ala-Phe-CH2Cl [AAF-CMK] (5 mg vial) alanyl-alanyl-phenylalanine chloromethyl ketone Alanyl-alanyl-phenylalanine chloromethyl ketone H-Ala-Ala-Phe-CMK Ala-ala-phe-chloromethyl ketone |
| Description | AAF-CMK is a TPPII (tripeptidylpeptidase II) inhibitor, shows anti-tumor activity and induces apoptosis. AAF-CMK can be used in leukemia research[1]. |
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| Related Catalog | |
| In Vitro | AAF-CMK (0-20 μM; 24 h) shows potentiated antitumor effects of U937 leukemia cells in combination with TRAIL or TNF[1]. AAF-CMK (20 μM; 24 h) increases TNF- and TRAIL-induced U937 cell apoptosis[1]. Cell Viability Assay[1] Cell Line: U937 human promonocytic leukemia cells Concentration: 0-20 μM Incubation Time: 24 h Result: Resulted in the potentiation of growth inhibitory cytostatic effects of TRAIL as well as TNF. Apoptosis Analysis[1] Cell Line: U937 human promonocytic leukemia cells Concentration: 20 μM Incubation Time: 24 h Result: Increased the percentage of apoptotic cells to 55.8% in combination with TRAIL. Increased number of cells with characteristic apoptotic morphology in groups treated with AAF-CMK and both TRAIL or TNF compared to each group treated alone. |
| Density | 1.215g/cm3 |
|---|---|
| Boiling Point | 508.9ºC at 760 mmHg |
| Molecular Formula | C16H22ClN3O3 |
| Molecular Weight | 339.81700 |
| Flash Point | 261.6ºC |
| Exact Mass | 339.13500 |
| PSA | 104.78000 |
| LogP | 2.30520 |
| Vapour Pressure | 1.78E-10mmHg at 25°C |
| Index of Refraction | 1.545 |