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Synonyms: MTP-PE, L-MTP-PE, CGP19835, CGP 19835

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $1,440 | Inquiry | Inquiry |
| Description | Mifamurtide (MTP-PE), an analog of muramyl dipeptide (MDP), is a nonspecific immunomodulator by stimulating the immune response activating macrophages and monocytes. Mifamurtide (MTP-PE) is a specific ligand for NOD2 and acts as an insulin sensitizer. Mifamurtide (MTP-PE) is used in immunology and rare disease research, including osteosarcoma-related experimental models, where Mifamurtide (MTP-PE) is applied to study innate immune receptor activation, macrophage polarization, and NOD2-associated signaling pathways in cellular immune response systems. |
| In vivo | Method:Thirty-three subjects were enrolled, including mild renal impairment (n=9), moderate renal impairment (n=8), and healthy subjects (n=16), to evaluate mifamurtide pharmacokinetics, pharmacodynamics, and safety across renal function groups. Result:Geometric mean (%CV) AUCinf for total mifamurtide was 89.5 (58.1), 94.8 (27.8), 85.1 (29.0), and 95.4 (18.1) nm·h in mild renal impairment, mild-matched healthy, moderate renal impairment, and moderate-matched healthy groups, respectively. Mifamurtide clearance was not correlated with CLcr, estimated GFR, or iohexol clearance (all r² < 0.01). AUCinf of free mifamurtide was similar across renal function groups. No apparent differences were observed in serum pharmacodynamic parameters (IL-6, TNF-α AUEClast and CRP Emax). No grade ≥3 or serious adverse events were reported. |
| Synonyms | MTP-PE, L-MTP-PE, CGP19835, CGP 19835 |
| Molecular Weight | 1237.50 |
| Formula | C59H109N6O19P |
| Cas No. | 83461-56-7 |
| Smiles | [C@H]([C@@H](NC(C)=O)C=O)(O[C@@H](C(N[C@H](C(N[C@H](CCC(N[C@H](C(NCCOP(OC[C@H](OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O)(=O)O)=O)C)=O)C(N)=O)=O)C)=O)C)[C@@H]([C@@H](CO)O)O |
| Relative Density. | 1.152g/cm3 |
| Sequence | MurNAc-Ala-D-Glu-dipalmitoyl-PE |
| Sequence Short | MurNAc-AE-DPPE |
| Storage | Store under nitrogen, Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (64.65 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween-80+45% Saline: 3.30 mg/mL (2.67 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
DMSO
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density. | |||||||||||||||||||||||||||||||
Dissolve 2 mg of the compound in 100 μL DMSO
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.
1) Add 100 μL of the DMSO
stock solution to 400 µL PEG300
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 ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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