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Z-VDVAD-FMK is a synthetic peptide that irreversibly inhibits the activity of caspase-2. It attenuates oxyhemoglobin-induced cleavage of PARP and apoptosis in endothelial cells. Z-VDVAD-FMK can be used for both in vitro and in vivo studies.
CAT No: R1111
CAS No: 210344-95-9
Synonyms/Alias: Z-DEVD-FMK;210344-95-9;Caspase-3 Inhibitor;C30H41FN4O12;L-Valinamide, N-[(phenylmethoxy)carbonyl]-L-alpha-aspartyl-L-alpha-glutamyl-N-[(1S)-3-fluoro-1-(2-methoxy-2-oxoethyl)-2-oxopropyl]-, 1,2-dimethyl ester;benzyloxycarbonyl-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-fluoromethylketone;methyl (4S)-5-[[(2S)-1-[[(3S)-5-fluoro-1-methoxy-1,4-dioxopentan-3-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-4-[[(2S)-4-methoxy-4-oxo-2-(phenylmethoxycarbonylamino)butanoyl]amino]-5-oxopentanoate;Z-Asp(OMe)-Glu(OMe)-Val-DL-Asp(OMe)-fluoromethylketone;Z-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-Fluoromethylketone;Z-Asp(O-Me)-Glu(O-Me)-Val-Asp(O-Me) fluoromethyl ketone;N-benzyloxycarbonyl-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-fluoromethyl ketone;methyl (5S,8S,11S,14S)-14-(2-fluoroacetyl)-11-isopropyl-5-(2-methoxy-2-oxoethyl)-8-(3-methoxy-3-oxopropyl)-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate;MFCD23380217;Z-DEVD-fluoromethylketone;Z-DEVD-fluoromethyl ketone;specific inhibitor of caspase-3;CHEMBL3963349;SCHEMBL18328791;DTXSID00879990;CHEBI:138013;BDBM228619;EX-A1761;HB1282;US9345789, Z-DEVD-FMK;AKOS024456968;CS-3454;AC-31504;BP-23680;BS-16593;DA-68816;FA111066;HY-12466;D71045;Z-Asp(OCH3)-Glu(OCH3)-Val-Asp(OCH3)-CH2F;Q60998625;benzyloxycarbonyl-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-fluoromethyl ketone;N-benzyloxycarbonyl-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-fluoromethyl-ketone;Z-Asp(O-Me)-Glu(O-Me)-Val-Asp(O-Me) fluoromethyl ketone, >=90% (HPLC);(5S,8S,11S,14S)-methyl 14-(2-fluoroacetyl)-11-isopropyl-5-(2-methoxy-2-oxoethyl)-8-(3-methoxy-3-oxopropyl)-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate;METHYL (3S)-3-[(2S)-2-[(2S)-2-[(2S)-2-{[(BENZYLOXY)CARBONYL]AMINO}-4-METHOXY-4-OXOBUTANAMIDO]-5-METHOXY-5-OXOPENTANAMIDO]-3-METHYLBUTANAMIDO]-5-FLUORO-4-OXOPENTANOATE;methyl (4S)-5-{[(2S)-1-amino-3-methyl-1-oxobutan-2-yl]amino}-4-{[(2S)-2-{[(benzyloxy)carbonyl]amino}-4-methoxy-4-oxobutanoyl]amino}-5-oxopentanoate;methyl (5S,8S,11S,14S)-14-(fluoroacetyl)-11-isopropyl-5-(2-methoxy-2-oxoethyl)-8-(3-methoxy-3-oxopropyl)-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazahexadecan-16-oate;N-[(phenylmethoxy)carbonyl]-L-alpha-aspartyl-L-alpha-glutamyl-N-[(1S)-3-fluoro-1-(2-methoxy-2-oxoethyl)-2-oxopropyl]-L-valinamide, 1,2-dimethyl ester;
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M.F/Formula | C30H41FN4O12 |
M.W/Mr. | 668.7 |
Sequence | One Letter Code:XXVX Three Letter Code:Cbz-Asp(OMe)-Glu(OMe)-Val-Asp(OMe)-CH2F |
Labeling Target | Caspase-2 |
Application | Z-VDVAD-FMK (Caspase-2 inhibitor) is a cell-permeable, irreversible inhibitor of caspase-2. Caspase inhibitors play an important role in investigating biological processes. The caspase family of proteins function as key components of the apoptotic machinery and act to destroy specific target proteins which are critical to cellular longevity. |
Appearance | White lyophilised solid |
Purity | >98% |
Activity | Inhibitor |
Areas of Interest | Cell Biology Cancer |
Long-term Storage Conditions | Soluble in DMSO |
Solubility | -20 °C |
InChI | InChI=1S/C30H41FN4O12/c1-17(2)26(29(42)33-20(22(36)15-31)13-24(38)45-4)35-27(40)19(11-12-23(37)44-3)32-28(41)21(14-25(39)46-5)34-30(43)47-16-18-9-7-6-8-10-18/h6-10,17,19-21,26H,11-16H2,1-5H3,(H,32,41)(H,33,42)(H,34,43)(H,35,40)/t19-,20-,21-,26-/m0/s1 |
InChI Key | GBJVAVGBSGRRKN-JYEBCORGSA-N |
Isomeric SMILES | CC(C)[C@@H](C(=O)N[C@@H](CC(=O)OC)C(=O)CF)NC(=O)[C@H](CCC(=O)OC)NC(=O)[C@H](CC(=O)OC)NC(=O)OCC1=CC=CC=C1 |
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