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Ablukast
Catalog No. T26519Cas No. 96566-25-5
Alias Ro 23-3544
Ablukast (Ro 23-3544) is a leukotriene receptor antagonist that functions as an anti-asthmatic.
Ablukast
Catalog No. T26519Alias Ro 23-3544Cas No. 96566-25-5
Ablukast (Ro 23-3544) is a leukotriene receptor antagonist that functions as an anti-asthmatic.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $41 | In Stock | |
| 5 mg | $116 | In Stock | |
| 10 mg | $188 | In Stock | |
| 25 mg | $371 | In Stock | |
| 50 mg | $521 | In Stock | |
| 100 mg | $708 | In Stock | |
| 200 mg | $953 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $128 | In Stock |
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Montelukast sodium
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Montelukast sodium (MK0476) is an orally available leukotriene receptor antagonist which is widely used for the prophylaxis and chronic treatment of asthma and has been linked to rare cases of clinically apparent liver injury.
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L 674573
L-674573, L674573, L-674,573, L674,573, L 674,573
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ABT-080 (VML 530), a leukotriene synthesis inhibitor, is used potentially for treatment of asthma.
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CGP 35949
CGP-35949, Cgp-35949, Cgp35949, CGP35949
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Montelukast
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Montelukast (Singular) is an orally available leukotriene receptor antagonist which is widely used for the prophylaxis and chronic treatment of asthma and has been linked to rare cases of clinically apparent liver injury.
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CitedREV 5901A
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REV 5901A (REV 5901 HCl) is an orally active leukotriene receptor antagonist and 5-lipoxygenase inhibitor with antimicrobial activity that attenuates colon cancer growth in mice.REV 5901A has been used in studies of asthma and myocardial infarction. REV 5901A is used to study asthma and myocardial infarction.
- $195
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Masilukast
ZD-3523, SA-09012, MCC-847, ICI-D-3523, ICI D-3523, D-3523
T27979136564-68-6In house
Masilukast(MCC-847) is an oral leukotriene D4 (LTD4) receptor antagonist for the study of diseases associated with inflammation.
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MK-571 sodium Cited
Verlukast sodium, Propanoic acid, MK-571 sodium salt, MK571, L-660711 sodium salt, L-660711 (sodium salt), L-660711
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MK-571 sodium (L-660711 sodium salt) is a selective, orally active antagonist of the CysLT1 receptor. MK-571 sodium is a multidrug resistance protein-2 (ABCC2, Mrp2) inhibitor used to demonstrate the role of Mrp2 in the cellular efflux of drugs, xenobiotics, and their conjugates. MK-571 sodium can inhibit the synthesis of K-4′-O-GlcA (19.7 μM). MK571 dose-dependently inhibits the intracellular biosynthesis of all flavonol sulphates and glucuronides by Caco-2 cells. MK-571 sodium significantly inhibits phase-2 conjugation of kaempferol by cell-free extracts of Caco-2, and production of kaempferol-4′-O-glucuronide was competitively inhibited. In addition to inhibiting MRP2, MK571 is a potent inhibitor of enterocyte phase-2 conjugation.
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CitedPranlukast Cited
ONO-1078
T0694103177-37-3
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CitedL 651896
L-651896, L651896
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L 651896 is a novel leukotriene biosynthesis and 5-lipoxygenase inhibitor for the study of respiratory and cardiovascular diseases.
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LY255283
LY 255283
T22946117690-79-6
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RG 7152
RG-7152, RG7152
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Purity:99.18%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | Ablukast (Ro 23-3544) is a leukotriene receptor antagonist that functions as an anti-asthmatic. |
| Alias | Ro 23-3544 |
| Molecular Weight | 498.56 |
| Formula | C28H34O8 |
| Cas No. | 96566-25-5 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 60 mg/ml (120.35 mM)  | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
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DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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