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Ac-YVAD-CHO

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Catalog No. T19883Cas No. 143313-51-3
Alias L-709049, L709049, L 709049

Ac-YVAD-CHO (L 709049) is a selective and potent tetrapeptide interleukin 1β-converting enzyme (ICE) and caspase-1 (ICE)-like protease inhibitor with anti-inflammatory activity, inhibits cancer cell growth, and inhibits the production of mature IL-lβ. Ac-YVAD-CHO attenuates quinolinic acid-induced p53 increase and apoptosis in rat striatum.

Ac-YVAD-CHO

Ac-YVAD-CHO

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Purity: 96.49%
Catalog No. T19883Alias L-709049, L709049, L 709049Cas No. 143313-51-3
Ac-YVAD-CHO (L 709049) is a selective and potent tetrapeptide interleukin 1β-converting enzyme (ICE) and caspase-1 (ICE)-like protease inhibitor with anti-inflammatory activity, inhibits cancer cell growth, and inhibits the production of mature IL-lβ. Ac-YVAD-CHO attenuates quinolinic acid-induced p53 increase and apoptosis in rat striatum.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$73In StockIn Stock
5 mg$289In StockIn Stock
10 mg$428-In Stock
25 mg$698-In Stock
50 mg$968-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:96.49%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Ac-YVAD-CHO (L 709049) is a selective and potent tetrapeptide interleukin 1β-converting enzyme (ICE) and caspase-1 (ICE)-like protease inhibitor with anti-inflammatory activity, inhibits cancer cell growth, and inhibits the production of mature IL-lβ. Ac-YVAD-CHO attenuates quinolinic acid-induced p53 increase and apoptosis in rat striatum.
Targets&IC50
IL-1β (human):0.7 μM, IL-1β (mouse):2.5 μM
In vitro
Ac-YVAD-CHO reduced the elevation of IL-1β in LPS-treated plasma and peritoneal fluid.Ac-YVAD-CHO inhibited IL-1β with IC50=2.5 μM (mouse) and IC50=0.7 μM (human) in both mouse and human. [1]
15.6 μM Ac-YVAD-CHO inhibited NO-induced PARP cleavage and reduced NO-induced apoptosis in SNAP-treated thymocytes. [2]
In vivo
30 mg/kg intraperitoneal injection of Ac-YVAD-CHO inhibited IL-1β levels in the blood of P. acnes sensitized mice. [1]
Intrastriatal infusion of 2-8 μg Ac-YVAD-CHO attenuated quinolinic acid (QA)-induced apoptosis in rat striatum. [3]
SynonymsL-709049, L709049, L 709049
Chemical Properties
Molecular Weight492.52
FormulaC23H32N4O8
Cas No.143313-51-3
Smiles[C@@H](NC([C@H](CC1=CC=C(O)C=C1)NC(C)=O)=O)(C(N[C@H](C(N[C@@H](CC(O)=O)C=O)=O)C)=O)C(C)C
Relative Density.1.276 g/cm3 (Predicted)
SequenceAc-Tyr-Val-Ala-Asp-al
Sequence ShortYVAD-CHO
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 50 mg/mL (101.52 mM), Sonication is recommended.
DMSO: 2 mg/mL (4.06 mM), Sonication is recommended.
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM2.0304 mL10.1519 mL20.3037 mL101.5187 mL
H2O
1mg5mg10mg50mg
5 mM0.4061 mL2.0304 mL4.0607 mL20.3037 mL
10 mM0.2030 mL1.0152 mL2.0304 mL10.1519 mL
20 mM0.1015 mL0.5076 mL1.0152 mL5.0759 mL
50 mM0.0406 mL0.2030 mL0.4061 mL2.0304 mL
100 mM0.0203 mL0.1015 mL0.2030 mL1.0152 mL

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TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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