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MW 630.7 Da, Purity >98%. Z-YVAD-FMK, Irreversible caspase-1 inhibitor. Achieve your results faster with highly validated, pure and trusted compounds.

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Images

Chemical Structure - Z-YVAD-FMK, Irreversible caspase-1 inhibitor (AB141388), expandable thumbnail
  • Cellular Activation - Z-YVAD-FMK, Irreversible caspase-1 inhibitor (AB141388), expandable thumbnail
  • Functional Studies - Z-YVAD-FMK, Irreversible caspase-1 inhibitor (AB141388), expandable thumbnail

Publications

Key facts

Purity

> 98%

Form

Lyophilized

Molecular weight

630.7 Da

Molecular formula

C31H39FN4O9

PubChem identifier

16760349

Nature

Synthetic

Recommended products

MW 630.7 Da, Purity >98%. Z-YVAD-FMK, Irreversible caspase-1 inhibitor. Achieve your results faster with highly validated, pure and trusted compounds.

Key facts

Purity

> 98%

PubChem identifier

16760349

Solubility

Soluble in DMSO to 20 mM.

Biochemical name

Caspase-1 Inhibitor VI

Canonical SMILES

CC(C)C(C(=O)NC(C)C(=O)NC(CC(=O)OC)C(=O)CF)NC(=O)C(CC1=CC=C(C=C1)O)NC(=O)OCC2=CC=CC=C2

Isomeric SMILES

C[C@@H](C(=O)N[C@@H](CC(=O)OC)C(=O)CF)NC(=O)[C@H](C(C)C)NC(=O)C(CC1=CC=C(C=C1)O)NC(=O)OCC2=CC=CC=C2

InChI

InChI=1S/C31H39FN4O9/c1-18(2)27(30(42)33-19(3)28(40)34-23(25(38)16-32)15-26(39)44-4)36-29(41)24(14-20-10-12-22(37)13-11-20)35-31(43)45-17-21-8-6-5-7-9-21/h5-13,18-19,23-24,27,37H,14-17H2,1-4H3,(H,33,42)(H,34,40)(H,35,43)(H,36,41)/t19-,23-,24?,27-/m0/s1

InChIKey

MVPQJUFFTWWKBT-UYDLRUHXSA-N

IUPAC name

methyl (3S)-5-fluoro-3-[[(2S)-2-[[(2S)-2-[[3-(4-hydroxyphenyl)-2-(phenylmethoxycarbonylamino)propanoyl]amino]-3-methylbutanoyl]amino]propanoyl]amino]-4-oxopentanoate

Storage

Shipped at conditions

Ambient - Can Ship with Ice

Appropriate long-term storage conditions

-20°C

Storage information

Store under desiccating conditions, The product can be stored for up to 12 months

Notes

This product is manufactured by BioVision, an Abcam company and was previously called 1141 YVAD-FMK, Z-,. 1141-5 is the same size as the 5 mg size of ab141388.

Product promise

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3 product images

  • Chemical Structure - Z-YVAD-FMK, Irreversible caspase-1 inhibitor (ab141388), expandable thumbnail

    Chemical Structure - Z-YVAD-FMK, Irreversible caspase-1 inhibitor (ab141388)

    2D chemical structure image of ab141388, Z-YVAD-FMK, Irreversible caspase-1 inhibitor

  • Cellular Activation - Z-YVAD-FMK, Irreversible caspase-1 inhibitor (ab141388), expandable thumbnail
    Image from Migita K, et al. Plos One, 9(5), e96703. Fig 3a,; doi: 10.1371/journal.pone.0096703

    Cellular Activation - Z-YVAD-FMK, Irreversible caspase-1 inhibitor (ab141388)

    Neutrophils were stimulated with SAA (5 µg/ml) in the presence or absence of Z-YVAD-FMK for 8 h. After stimulation, supernatants were analyzed for IL-1 Β production using ELISA. Values represent the mean ± SD of two independent experiments. *p<0.001 compared to SAA-stimulated neutrophils.

  • Functional Studies - Z-YVAD-FMK, Irreversible caspase-1 inhibitor (ab141388), expandable thumbnail

    Functional Studies - Z-YVAD-FMK, Irreversible caspase-1 inhibitor (ab141388)

    SHSY5Y cells were incubated at 37°C for 1h with vehicle control (0 μM) and different concentrations of Z-YVAD-FMK (ab141388). After this incubation 10 μM of camptothecin (Camptothecin, DNA topoisomerase inhibitor ab120115) was added to all samples and the cells were incubated for further 24h. Increased expression of full length PARP (ab37722) in camptothecin induced apoptotic SHSY5Y cells correlates with an increase in Z-YVAD-FMK concentration, as described in literature.

    Whole cell lysates were prepared with RIPA buffer (containing protease inhibitors and sodium orthovanadate), 20 μg of each were loaded on the gel and the WB was run under reducing conditions. After transfer the membrane was blocked for an hour using 3% milk before being incubated with ab37722 at 1 μg/ml and Anti-beta Actin antibody ab8227 at 1 μg/ml overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/10000 dilution and visualised using ECL development so

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Product protocols

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