Ac-Asp-Glu-Val-Asp-aldehyde (pseudo acid)

Ac-Asp-Glu-Val-Asp-aldehyde (pseudo acid) contains a reactive aldehyde functionality that allows covalent interaction with nucleophilic targets. Its structure makes it a powerful tool in protease mechanism studies and transition-state modeling. The peptide's controlled reactivity enables detailed examination of enzymatic cleavage pathways. Its stability and versatility support diverse biochemical research applications.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: C11055

CAS No:184179-08-6

Synonyms/Alias:Ac-DEVD-CHO;169332-60-9;184179-08-6;N-acetyl-asp-glu-val-asp-al;AC-ASP-GLU-VAL-ASP-H;Caspase-3 Inhibitor I;(4S,7S,10S,13S)-7-(2-carboxyethyl)-4-(carboxymethyl)-13-formyl-10-isopropyl-2,5,8,11-tetraoxo-3,6,9,12-tetraazapentadecan-15-oic acid;Ac-Asp-Glu-Val-Asp-Aldehyde;CHEMBL417149;CHEBI:59385;(4S)-4-[[(2S)-2-acetamido-3-carboxypropanoyl]amino]-5-[[(2S)-1-[[(2S)-1-carboxy-3-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-5-oxopentanoic acid;Ac-Asp-Glu-Val-Asp-aldehyde (pseudo acid);L-Valinamide,N-acetyl-L-a-aspartyl-L-a-glutamyl-N-(2-carboxy-1-formylethyl)-;acetyl-Asp-Glu-Val-Asp aldehyde;acetyl-Asp-Glu-Val-Asp-aldehyde;N-acetyl-Asp-Glu-Val-Asp aldehyde;N-acetyl-Asp-Glu-Val-Asp-aldehyde;acetyl-aspartyl-glutamyl-valyl-aspartal;C20H30N4O11;MF 191;2h5i;Ac-Asp-Glu-Val-Asp aldehyde;GTPL6527;SCHEMBL1674857;BDBM10246;DTXSID40937624;UMBVAPCONCILTL-MRHIQRDNSA-N;HY-P1001;s7901;AKOS037648768;CCG-269708;CS-7676;NCGC00345452-02;(4S)-4-[[(2S)-2-acetamido-4-hydroxy-4-oxobutanoyl]amino]-5-[[(2S)-1-[[(2S)-4-hydroxy-1,4-dioxobutan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-5-oxopentanoic acid;AC-29039;BS-15530;DA-60711;FA108687;D71136;Caspase-3 Inhibitor I - CAS 169332-60-9;L 761191;Q27074145;Z4561822377;L-valinamide, N-acetyl-L-alpha-aspartyl-L-alpha-glutamyl-N-[(1S)-2-carboxy-1-formylethyl]-;N-acetyl-L-alpha-aspartyl-L-alpha-glutamyl-N-[(1S)-2-carboxy-1-formylethyl]-L-valinamide;(4S)-4-{[(1S)-1-{[(2S)-1-carboxy-3-oxopropan-2-yl]carbamoyl}-2-methylpropyl]carbamoyl}-4-[(3S)-3-acetamido-3-formamidopropanoic acid]butanoic acid;(4S,7S,10S,13S)-7-(2-carboxyethyl)-4-(carboxymethyl)-13-formyl-10-isopropyl-2,5,8,11-tetraoxo-3,6,9,12-tetraazapentadecan-15-oicacid;7-(2-Carboxyethyl)-4-(carboxymethyl)-13-formyl-2,5,8,11-tetrahydroxy-10-(propan-2-yl)-3,6,9,12-tetraazapentadeca-2,5,8,11-tetraen-15-oic acid;L-Valinamide, N-acetyl-L-alpha-aspartyl-L-alpha-glutamyl-N-(2-carboxy-1-formylethyl)-, (S)-;L-Valinamide, N-acetyl-L-alpha-aspartyl-L-alpha-glutamyl-N-[(1S)-2-carboxy-1-formylethyl]- (9CI);N-acetyl-L-alpha-aspartyl-L-alpha-glutamyl-N-[(2S)-1-carboxy-3-oxopropan-2-yl]-L-valinamide;

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M.F/Formula
C20H30N4O11
M.W/Mr.
502.5
Sequence
One Letter Code:DEVD
Three Letter Code:Ac-Asp-Glu-Val-Asp-al
InChI
InChI=1S/C20H30N4O11/c1-9(2)17(20(35)22-11(8-25)6-15(29)30)24-18(33)12(4-5-14(27)28)23-19(34)13(7-16(31)32)21-10(3)26/h8-9,11-13,17H,4-7H2,1-3H3,(H,21,26)(H,22,35)(H,23,34)(H,24,33)(H,27,28)(H,29,30)(H,31,32)/t11-,12-,13-,17-/m0/s1
InChI Key
UMBVAPCONCILTL-MRHIQRDNSA-N

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