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Macrophage-activating lipopeptide 2 TFA

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Catalog No. TP2905
Alias MALP-2 TFA

Macrophage-activating lipopeptide 2 TFA (MALP-2 TFA) is a diacylglycerol lipopeptide and TLR-2/TLR-6 agonist that activates immune cell responses such as macrophages, upregulating TNF, IL-6, and PGE2 to induce local inflammation.

Macrophage-activating lipopeptide 2 TFA

Macrophage-activating lipopeptide 2 TFA

😃Good
Purity: 97.56%
Catalog No. TP2905Alias MALP-2 TFA
Macrophage-activating lipopeptide 2 TFA (MALP-2 TFA) is a diacylglycerol lipopeptide and TLR-2/TLR-6 agonist that activates immune cell responses such as macrophages, upregulating TNF, IL-6, and PGE2 to induce local inflammation.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$110In StockIn Stock
5 mg$280In StockIn Stock
10 mg$455-In Stock
25 mg$770-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:97.56%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Macrophage-activating lipopeptide 2 TFA (MALP-2 TFA) is a diacylglycerol lipopeptide and TLR-2/TLR-6 agonist that activates immune cell responses such as macrophages, upregulating TNF, IL-6, and PGE2 to induce local inflammation.
In vitro
Method:
Endothelial cells, including MyEnd cells, were treated with Macrophage-activating lipopeptide 2 TFA (1 µg/mL) for 24 hours and 2 hours, respectively, to assess its effects on the expression of leukocyte adhesion molecules and activation of signaling pathways.

Result:
Treatment with Macrophage-activating lipopeptide 2 TFA (1 µg/mL) for 24 hours upregulated the expression of key endothelial adhesion molecules and leukocyte integrin receptors, thereby enhancing leukocyte adhesion to endothelial cells. A 2-hour treatment promoted the phosphorylation of protein kinase B (Akt) and eNOS in MyEnd cells, leading to increased nitric oxide (NO) release. [1]
In vivo
Method:
A lower limb ischemia model was established in hypercholesterolemic Apoe-deficient mice by performing experimental femoral artery ligation (FAL). Mice were then treated with Macrophage-activating lipopeptide 2 TFA (1 µg dissolved in 125 µL PBS) via intravenous injection once daily for 10 consecutive days. The effects on hindlimb perfusion recovery and collateral vessel growth were evaluated.

Result:
Intravenous administration of Macrophage-activating lipopeptide 2 TFA significantly improved hindlimb perfusion recovery and promoted collateral vessel growth in Apoe-deficient mice following FAL. [1]
SynonymsMALP-2 TFA
Chemical Properties
Molecular Weight2135.56 (free base)
FormulaC99H167N19O30S.xC2HF3O2
SmilesNC(C[C@@H](C(N[C@H](C(N[C@@H](CC(O)=O)C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@]([H])(C(N[C@H](C(N[C@@H](CC1=CC=CC=C1)C(N[C@H](C(N[C@H](C(N[C@H](C(O)=O)CCCCN)=O)CCC(O)=O)=O)CCCCN)=O)=O)CO)=O)[C@@H](C)CC)=O)CC(N)=O)=O)CO)=O)CCC(O)=O)=O)=O)CC(N)=O)=O)NC(CNC([C@H](N)CSC[C@H](COC(CCCCCCCCCCCCCCC)=O)OC(CCCCCCCCCCCCCCC)=O)=O)=O)=O.OC(C(F)(F)F)=O
Sequence{S-[(2R)-2,3-bis[(1-oxohexadecyl)oxy]propyl]Cys}-Gly-Asn-Asn-Asp-Glu-Ser-Asn-Ile-Ser-Phe-Lys-Glu-Lys
Sequence Short{S-[(2R)-2,3-bis[(1-oxohexadecyl)oxy]propyl]Cys}-GNNDESNISFKEK
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: 1.5 mg/mL, when pH is adjusted to 12 with 1M NaOH. Sonication is recommended.
DMSO: 40 mg/mL, Sonication is recommended.

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
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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