MeOSuc-Ala-Ala-Pro-Val-Chloromethylketone
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MeOSuc-Ala-Ala-Pro-Val-Chloromethylketone

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MeOSuc-Ala-Ala-Pro-Val-Chloromethylketone is an irreversible inhibitor of human leukocyte and neutrophil elastase with a Ki = 10 µM.

Category
Peptide Inhibitors
Catalog number
BAT-015741
CAS number
65144-34-5
Molecular Formula
C22H35ClN4O7
Molecular Weight
502.99
MeOSuc-Ala-Ala-Pro-Val-Chloromethylketone
IUPAC Name
methyl 4-[[(2S)-1-[[(2S)-1-[(2S)-2-[[(3S)-1-chloro-4-methyl-2-oxopentan-3-yl]carbamoyl]pyrrolidin-1-yl]-1-oxopropan-2-yl]amino]-1-oxopropan-2-yl]amino]-4-oxobutanoate
Synonyms
Msaapvck; Meosuc-aapv-cmk; methoxysuccinyl-alanyl-alanyl-prolyl-valine chloromethyl ketone; N-(Methoxysuccinyl)-Ala-Ala-Pro-Val-chloromethyl ketone
Purity
95%
Density
1.234g/cm3
Melting Point
159-161ºC
Boiling Point
809.4ºC at 760 mmHg
Sequence
MeOSuc-Ala-Ala-Pro-Val-CH2Cl
Storage
-20ºC
Solubility
Soluble in DMSO (10 mg/mL), and methanol (50 mg/mL)
Application
Serine Proteinase Inhibitors
InChI
InChI=1S/C22H35ClN4O7/c1-12(2)19(16(28)11-23)26-21(32)15-7-6-10-27(15)22(33)14(4)25-20(31)13(3)24-17(29)8-9-18(30)34-5/h12-15,19H,6-11H2,1-5H3,(H,24,29)(H,25,31)(H,26,32)/t13-,14-,15-,19-/m0/s1
InChI Key
PJGDFLJMBAYGGC-XLPNERPQSA-N
Canonical SMILES
CC(C)C(C(=O)CCl)NC(=O)C1CCCN1C(=O)C(C)NC(=O)C(C)NC(=O)CCC(=O)OC
1. Quantification of elastase-like activity in 13 human cancer cell lines and in an immortalized human epithelial cell line by RP-HPLC
Patrick J Bednarski, Karin Achilles Biol Chem . 2003 May;384(5):817-24. doi: 10.1515/BC.2003.091.
A sensitive and specific RP-HPLC assay was developed to measure the levels of polymorphonuclear elastase (PMN-E) activity in growing cell cultures. By combining a pre-incubation of the cells with a relatively non-toxic, PMN-E-specific inhibitor, MeOSuc-Ala-Ala-Pro-Val-chloromethylketone (MAAPVCK), the p-nitroaniline formed by the hydrolysis of the substrate MeOSuc-Ala-Ala-Pro-Val-p-NA by PMN-E is quantified. Elastase-like activity was measured in 14 human cells lines: 13 cancer cell lines (HL-60, U-937, A-427, LCLC-103H, YAPC, DAN-G, PA-TU-8902, KYSE-70, -510, -520, 5637, SISO and MCF-7) and one immortalized epithelial cell line (hTert-RPE1). Activity was detected in all lines; the lowest was found in hTert-RPE1 cells while the highest was detected in a pancreas adenocarcinoma line (PA-TU-8902). When the results were normalized according to cell volume instead of cell number, the leukemia line HL-60 had the highest activity and PA-TU-8902 ranked second. A 1 h pre-incubation with 9.0 microM of the irreversible PMN-E inhibitor MAAPVCK led to varying degrees of enzyme inhibition depending on the cell line; the strongest inhibition was observed with the PA-TU-8902 pancreatic cancer cell line (90% inhibition) while the weakest was seen with the A-427 lung cancer cell line (52%). These results indicate that PA-TU-8902 is a suitable in vitro model for testing the efficacy of PMN-E-activated prodrugs of antitumor agents.
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