Z-VAD-FMK C22H30FN307 

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Z-VAD-FMK
HY-16658B 10mg
EUR 786

Z-VAD-FMK
13300 1 mg
EUR 102

Z-VAD(OMe)-FMK
HY-16658 10mg
EUR 472.8

Z-VAD-FMK, cell permeable
GL1523-1MG 1 mg
EUR 330

Z-VAD-FMK, cell permeable
GL1523-5MG 5 mg
EUR 950.4

Caspase-Family Inhibitor Z-VAD-FMK
1010-100
EUR 235.2

Caspase-Family Inhibitor Z-VAD-FMK
1010-20C
EUR 235.2

SRB-VAD-FMK [Sulforhodamine B-VAD-FMK]
13472 25 Tests
EUR 158.4

SRB-VAD-FMK [Sulforhodamine B-VAD-FMK]
13482 100 Tests
EUR 211

Z-VAD-FMK (Pan-specific caspase inhibitor)
SIH-557-1MG 1 mg
EUR 231.6
Description: The substance Z-VAD-FMK is a pan-specific caspase inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is lyophilized solid or wax which is May be dissolved in DMSO (10 mg/ml).

Biotin-VAD-FMK
1123-20C
EUR 392.4

FAM-VAD-FMK
13470 25 Tests
EUR 158.4

TF4-VAD-FMK
13471 25 Tests
EUR 158.4

FITC-VAD-FMK
9497-100
EUR 430.8

Biotin-VAD-FMK
HY-100894 1mg
EUR 1216.8

FAM-VAD-FMK
13484 100 Tests
EUR 211

mFluor™ 450-VAD-FMK
13475 25 Tests
EUR 158.4

mFluor™ 510-VAD-FMK
13476 25 Tests
EUR 158.4

Z-YVAD-FMK
A8955-1 1 mg
EUR 282
Description: Z-YVAD-FMK is a potent cell-permeable and irreversible inhibitor of caspase-1.In Caco-2 cells, Z-YVAD-FMK significantly decreased the growth inhibition induced by butyrate.

Z-YVAD-FMK
A8955-5 5 mg
EUR 616.8
Description: Z-YVAD-FMK is a potent cell-permeable and irreversible inhibitor of caspase-1.In Caco-2 cells, Z-YVAD-FMK significantly decreased the growth inhibition induced by butyrate.

Z-YVAD-FMK
A8955-5.1 10 mM (in 1mL DMSO)
EUR 1326
Description: Z-YVAD-FMK is a potent cell-permeable and irreversible inhibitor of caspase-1.In Caco-2 cells, Z-YVAD-FMK significantly decreased the growth inhibition induced by butyrate.

Z-YVAD-FMK
1141-1
EUR 405.6

Z-YVAD-FMK
1141-5
EUR 966

Z-VDVAD-FMK
1142-1
EUR 366

Z-VDVAD-FMK
1142-5
EUR 966

Z-DEVD-FMK
1143-1
EUR 379.2

Z-DEVD-FMK
1143-5
EUR 966

Z-LEVD-FMK
1144-1
EUR 379.2

Z-LEVD-FMK
1144-5
EUR 966

Z-VEID-FMK
1146-1
EUR 366

Z-VEID-FMK
1146-5
EUR 966

Z-IETD-FMK
1148-1
EUR 392.4

Z-IETD-FMK
1148-5
EUR 940.8

Z-LEHD-FMK
1149-1
EUR 379.2

Z-LEHD-FMK
1149-5
EUR 920.4

Z-ATAD-FMK
1152-1
EUR 418.8

Z-ATAD-FMK
1152-5
EUR 1096.8

Z-FA-FMK
1986-1
EUR 176.4

Z-FA-FMK
1986-5
EUR 444

Z-FA-FMK
A8170-1 1 mg
EUR 142.8
Description: Z-FA-FMK is a control peptidic fluoromethylketone (boc-Thr-CH2F), and inhibitor to calpain (Ac-Leu-Leu-norleucinal), cathepsin B (Z-Phe-Ala-CH2F), and CPP32-like proteases (Z-DEVD-CH2F) [1].

Z-FA-FMK
A8170-10 10 mg
EUR 560.4
Description: Z-FA-FMK is a control peptidic fluoromethylketone (boc-Thr-CH2F), and inhibitor to calpain (Ac-Leu-Leu-norleucinal), cathepsin B (Z-Phe-Ala-CH2F), and CPP32-like proteases (Z-DEVD-CH2F) [1].

Z-FA-FMK
A8170-25 25 mg
EUR 616.8
Description: Z-FA-FMK is a control peptidic fluoromethylketone (boc-Thr-CH2F), and inhibitor to calpain (Ac-Leu-Leu-norleucinal), cathepsin B (Z-Phe-Ala-CH2F), and CPP32-like proteases (Z-DEVD-CH2F) [1].

Z-FA-FMK
A8170-5 5 mg
EUR 338.4
Description: Z-FA-FMK is a control peptidic fluoromethylketone (boc-Thr-CH2F), and inhibitor to calpain (Ac-Leu-Leu-norleucinal), cathepsin B (Z-Phe-Ala-CH2F), and CPP32-like proteases (Z-DEVD-CH2F) [1].

Z-FA-FMK
A8170-5.1 10 mM (in 1mL DMSO)
EUR 408
Description: Z-FA-FMK is a control peptidic fluoromethylketone (boc-Thr-CH2F), and inhibitor to calpain (Ac-Leu-Leu-norleucinal), cathepsin B (Z-Phe-Ala-CH2F), and CPP32-like proteases (Z-DEVD-CH2F) [1].

Z-FA-FMK
A8170-S Evaluation Sample
EUR 97.2
Description: Z-FA-FMK is a control peptidic fluoromethylketone (boc-Thr-CH2F), and inhibitor to calpain (Ac-Leu-Leu-norleucinal), cathepsin B (Z-Phe-Ala-CH2F), and CPP32-like proteases (Z-DEVD-CH2F) [1].

Z-DEVD-FMK
A1920-1 1 mg
EUR 135.6
Description: Z-DEVD-FMK is a tetrapeptide caspase inhibitor that is considered relatively selective for caspase-31, 2 and has been widely used in in vitro and in vivo models of acute injury to delineate roles for caspase 3 in neuronal cell death.

Z-DEVD-FMK
A1920-10 10 mg
EUR 408
Description: Z-DEVD-FMK is a tetrapeptide caspase inhibitor that is considered relatively selective for caspase-31, 2 and has been widely used in in vitro and in vivo models of acute injury to delineate roles for caspase 3 in neuronal cell death.

Z-DEVD-FMK
A1920-25 25 mg
EUR 616.8
Description: Z-DEVD-FMK is a tetrapeptide caspase inhibitor that is considered relatively selective for caspase-31, 2 and has been widely used in in vitro and in vivo models of acute injury to delineate roles for caspase 3 in neuronal cell death.

Z-DEVD-FMK
A1920-5 5 mg
EUR 268.8
Description: Z-DEVD-FMK is a tetrapeptide caspase inhibitor that is considered relatively selective for caspase-31, 2 and has been widely used in in vitro and in vivo models of acute injury to delineate roles for caspase 3 in neuronal cell death.

Z-DEVD-FMK
A1920-5.1 10 mM (in 1mL DMSO)
EUR 351.6
Description: Z-DEVD-FMK is a tetrapeptide caspase inhibitor that is considered relatively selective for caspase-31, 2 and has been widely used in in vitro and in vivo models of acute injury to delineate roles for caspase 3 in neuronal cell death.

Z-DEVD-FMK
A1920-S Evaluation Sample
EUR 97.2
Description: Z-DEVD-FMK is a tetrapeptide caspase inhibitor that is considered relatively selective for caspase-31, 2 and has been widely used in in vitro and in vivo models of acute injury to delineate roles for caspase 3 in neuronal cell death.

Z-DQMD-FMK
A1921-1 1 mg
EUR 135.6
Description: Inhibition of caspase-3 processing by Z-DQMD-FMK (Z-Asp(OMe)-Gln-Met-Asp(OMe)-fluoromethylketone) did not restore cell number in the zinc-deficient group, but resulted in processing of full-length PKC-? to a 56-kDa fragment1.

Z-DQMD-FMK
A1921-10 10 mg
EUR 408
Description: Inhibition of caspase-3 processing by Z-DQMD-FMK (Z-Asp(OMe)-Gln-Met-Asp(OMe)-fluoromethylketone) did not restore cell number in the zinc-deficient group, but resulted in processing of full-length PKC-? to a 56-kDa fragment1.

Z-DQMD-FMK
A1921-25 25 mg
EUR 616.8
Description: Inhibition of caspase-3 processing by Z-DQMD-FMK (Z-Asp(OMe)-Gln-Met-Asp(OMe)-fluoromethylketone) did not restore cell number in the zinc-deficient group, but resulted in processing of full-length PKC-? to a 56-kDa fragment1.

Z-DQMD-FMK
A1921-5 5 mg
EUR 268.8
Description: Inhibition of caspase-3 processing by Z-DQMD-FMK (Z-Asp(OMe)-Gln-Met-Asp(OMe)-fluoromethylketone) did not restore cell number in the zinc-deficient group, but resulted in processing of full-length PKC-? to a 56-kDa fragment1.

Z-DQMD-FMK
A1921-5.1 10 mM (in 1mL DMSO)
EUR 518.4
Description: Inhibition of caspase-3 processing by Z-DQMD-FMK (Z-Asp(OMe)-Gln-Met-Asp(OMe)-fluoromethylketone) did not restore cell number in the zinc-deficient group, but resulted in processing of full-length PKC-? to a 56-kDa fragment1.

Z-VAD-FMK C22H30FN307