Z-Asp-2,6-dichlorobenzoyloxymethylketone

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Company Name: VDM Biochemicals   
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Z-Asp-2,6-dichlorobenzoyloxymethylketone manufacturers

  • Z-Asp-CH2-DCB
  • Z-Asp-CH2-DCB pictures
  • 2026-07-27
  • CAS:153088-73-4
  • Purity: 99.08%
  • Supply Ability: 10g
  • Z-Asp-CH2-DCB
  • Z-Asp-CH2-DCB pictures
  • 2026-07-23
  • CAS:153088-73-4
  • Purity: 99.08%
  • Supply Ability: 10g
Z-Asp-2,6-dichlorobenzoyloxymethylketone Basic information
Product Name:Z-Asp-2,6-dichlorobenzoyloxymethylketone
Synonyms:ICE INHIBITOR V;ICE INHIBITOR VI;CASPASE-1 INHIBITOR V;CASPASE-1 INHIBITOR III;(BENZYLOXYCARBONYL-L-ASPART-1-YL)[(2,6-DICHLOROBENZOYL)OXY]METHANE;Z-ASP-[(2,6-DICHLOROBENZOYL)OXY]METHANE;Z-D-CH2-DCB;Z-ASP-CH2-DCB
CAS:153088-73-4
MF:C20H17Cl2NO7
MW:454.26
EINECS:
Product Categories:Pepetides;peptides;Caspase/Related Products
Mol File:153088-73-4.mol
Z-Asp-2,6-dichlorobenzoyloxymethylketone Structure
Z-Asp-2,6-dichlorobenzoyloxymethylketone Chemical Properties
Boiling point 674.2±55.0 °C(Predicted)
density 1.440±0.06 g/cm3(Predicted)
storage temp. −20°C
solubility Soluble in DMSO (up to 25 mg/ml).
form White to off-white powder.
pka4.01±0.19(Predicted)
color white
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
Safety Information
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
Z-Asp-2,6-dichlorobenzoyloxymethylketone Usage And Synthesis
DescriptionZ-Asp-CH2-DCB is a peptide originally synthesized for its ability to inactivate the interleukin-1β-converting enzyme, which is the homolog of the C. elegans positive regulator of apoptosis CED-3. Z-Asp-CH2-DCB has been shown to block apoptosis by nonselectively inhibiting caspase activity. At 1-100 μM, it can dose-dependently block the production of IL-1β, TNF-α, IL-6, and IFN-γ by human peripheral blood mononuclear cells as well as inhibit T cell proliferation.
UsesZ-Asp-2,6-dichlorobenzoyloxymethylketone is a broad Caspase Inhibitor.
in vivo

Z-Asp-CH2-DCB (1 mg; i.p.; every day for 3 weeks) prevents SU5416-induced septal cell apoptosis[1].

Animal Model:Male Sprague-Dawley rats (SU5416+ Z-Asp-CH2-DCB group)[1]
Dosage:1 mg
Administration:Intraperitoneal injection; every day for 3 weeks
Result:The caspase 3-like activity in SU5416-treated rat lungs is significantly higher, whereas lungs from rats treated with SU5416+Z-Asp-CH2-DCB showed no increase in apoptotic activity.
References[1] ROLAND E. DOLLE. P1 Aspartate-Based Peptide .alpha.-((2,6-Dichlorobenzoyl)oxy)methyl Ketones as Potent Time-Dependent Inhibitors of Interleukin-1.beta.-Converting Enzyme[J]. Journal of Medicinal Chemistry, 1994, 37 5: 563-564. DOI:10.1021/jm00031a003
Z-Asp-2,6-dichlorobenzoyloxymethylketone Preparation Products And Raw materials
Tag:Z-Asp-2,6-dichlorobenzoyloxymethylketone(153088-73-4) Related Product Information
Z-Ala-Gly-OH Z-ASP-GLN-MET-ASP-AFC Z-ALA-SER-OH Z-ALA-PRO-PNA Z-ARG-PNA HCL CASPASE INHIBITOR3 Z-YVAD-AFC ALPHA-(TRICHLOROMETHYL)-4-PYRIDINEETHANOL AC-VDVAD-CHO AC-DEVD-AFC PAC1 AC-DEVD-CHO AC-VDVAD-PNA Z-VAD-FMK Ac-VEID-AMC Ac-Leu-Glu-Thr-Asp-AFC Ac-LEHD-AFC 2,6-Dichlorobenzyl methyl ether