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MK 571 (L660711) is an orally active antagonist of CysLT1 receptor.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 2 mg | $30 | In Stock | In Stock | |
| 5 mg | $48 | In Stock | In Stock | |
| 10 mg | $78 | In Stock | In Stock | |
| 25 mg | $177 | In Stock | In Stock | |
| 50 mg | $317 | In Stock | In Stock | |
| 100 mg | $479 | In Stock | In Stock | |
| 200 mg | $686 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $57 | In Stock | In Stock |
| Description | MK 571 (L660711) is an orally active antagonist of CysLT1 receptor. |
| Targets&IC50 | LTE4:10.4 (pA2, in guinea pig ileum), LTD4:2.1 nM (Ki, in human lung), LTD4:0.22 nM (Ki, in guinea pig lung), LTD4:10.5 (pA2, in guinea pig ileum) |
| In vivo | MK-571 effectively blocks LTD4 activation of recombinant human and murine CysLT1 receptors1,4 but is ineffective at blocking LTC4 or LTD4 activation of the recombinant human or murine CysLT2 receptors[1]. |
| Synonyms | MK-571, L-660711, L660711 |
| Molecular Weight | 515.09 |
| Formula | C26H27ClN2O3S2 |
| Cas No. | 115104-28-4 |
| Smiles | C(=C/C1=CC(C(SCCC(N(C)C)=O)SCCC(O)=O)=CC=C1)\C2=NC3=C(C=C2)C=CC(Cl)=C3 |
| Relative Density. | 1.327g/cm3 |
| Storage | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 62.5 mg/mL (121.34 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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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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