475874 Sigma-AldrichMK571, Sodium Salt - CAS 115104-28-4 - Calbiochem
A selective, competitive antagonist of leukotriene D4 (LTD4) (Ki = 2.1 nM for inhibition of [³H]LTD4 binding to human lung membranes).
More>> A selective, competitive antagonist of leukotriene D4 (LTD4) (Ki = 2.1 nM for inhibition of [³H]LTD4 binding to human lung membranes). Less<<Synonyms: L 660711, Sodium Salt, (E)-3-[[[3-[2-(7-Chloro-2-quinolinyl)ethenyl]phenyl]-[[3-dimethylamino)-3-oxopropyl]thio]methyl]thio]-propanoic Acid, Sodium Salt
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Overview
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Key Spec Table
| CAS # | Empirical Formula |
|---|---|
| 115104-28-4 | C₂₆H₂₆ClN₂O₃S₂ • Na |
Pricing & Availability
| Catalogue Number | Availability | Packaging | Qty/Pack | Price | Quantity | |
|---|---|---|---|---|---|---|
| 475874-5MG |
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Plastic ampoule | 5 mg |
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| References | |
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| References | Olson, D.P., et al. 2001. Cytometry 46, 105. Van der Kolk, D.M., et al. 1998. Clin. Cancer Res. 4, 1727. Jones, T.R., et al. 1989. Can. J. Physiol. Pharmacol. 67, 17. |
| Product Information | |
|---|---|
| CAS number | 115104-28-4 |
| ATP Competitive | N |
| Form | Off-white solid |
| Hill Formula | C₂₆H₂₆ClN₂O₃S₂ • Na |
| Chemical formula | C₂₆H₂₆ClN₂O₃S₂ • Na |
| HS Code | 2933 49 90 |
| Hygroscopic | Hygroscopic |
| Reversible | N |
| Structure formula Image | |
| Quality Level | MQ100 |
| Applications |
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| Biological Information | |
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| Primary Target | Antagonist of leukotriene D4 (LTD4) |
| Primary Target K<sub>i</sub> | 2.1 nM for inhibition of [3H]LTD4 binding to human lung membranes |
| Purity | ≥90% by HPLC |
| Physicochemical Information | |
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| Cell permeable | N |
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| Specifications |
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| Global Trade Item Number | |
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| Catalogue Number | GTIN |
| 475874-5MG | 07790788050474 |
Documentation
MK571, Sodium Salt - CAS 115104-28-4 - Calbiochem SDS
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MK571, Sodium Salt - CAS 115104-28-4 - Calbiochem Certificates of Analysis
| Title | Lot Number |
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| 475874 |
References
| Reference overview |
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| Olson, D.P., et al. 2001. Cytometry 46, 105. Van der Kolk, D.M., et al. 1998. Clin. Cancer Res. 4, 1727. Jones, T.R., et al. 1989. Can. J. Physiol. Pharmacol. 67, 17. |



