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Murepavadin TFA is a highly potent 14–amino acid cyclic peptide antibiotic that exhibits strong and specific antibacterial activity against Pseudomonas aeruginosa, with MIC50 and MIC90 values both measured at 0.12 mg/L, functioning through targeted interaction with the lipopolysaccharide transport protein D, and serving as a valuable research compound for studying bacterial resistance mechanisms, antimicrobial specificity, and novel antibiotic development strategies.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $117 | - | In Stock | |
| 5 mg | $289 | - | In Stock | |
| 10 mg | $455 | - | In Stock | |
| 25 mg | $889 | - | In Stock | |
| 50 mg | $1,360 | - | In Stock |
| Description | Murepavadin TFA is a highly potent 14–amino acid cyclic peptide antibiotic that exhibits strong and specific antibacterial activity against Pseudomonas aeruginosa, with MIC50 and MIC90 values both measured at 0.12 mg/L, functioning through targeted interaction with the lipopolysaccharide transport protein D, and serving as a valuable research compound for studying bacterial resistance mechanisms, antimicrobial specificity, and novel antibiotic development strategies. |
| In vivo | Method: Murepavadin TFA was administered subcutaneously at doses ranging from 0 to 100 mg/kg in preclinical infection models using XDR bacterial isolates. Result: Murepavadin TFA demonstrated antibacterial activity in preclinical animal infection models[1]. |
| Synonyms | POL7080 TFA, POL 7080 TFA, Murepavadin TFA |
| Molecular Weight | 1667.83 |
| Formula | C73H112N22O16.C2HF3O2 |
| Cas No. | 3053070-05-3 |
| Smiles | CC[C@H](C)[C@H]1C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N2CCC[C@@H]2C(=O)N3CCC[C@H]3C(=O)N[C@H](C(=O)N[C@H](C(=O)N1)CC4=CNC5=CC=CC=C54)[C@@H](C)O)CO)C)CCN)CCN)CC6=CNC7=CC=CC=C76)CCN)CCN)CCCN)CCN.C(=O)(C(F)(F)F)O |
| Sequence | Cyclo[Ala-Ser-dPro-Pro-Thr-Trp-Ile-Dab-Orn-dDab-Dab-Trp-Dab-Dab].CH3CO2H |
| Sequence Short | Cyclo(AS-{d-Pro}-PTWI-{Dab}-{Orn}-{d-Dab}-{Dab}-W-{Dab}-{Dab}) |
| Storage | keep away from moisture | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||
| Solubility Information | H2O: 40.00 mg/mL (23.98 mM), Sonication is recommended. | |||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||
H2O
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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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