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Zaloglanstat
🥰Excellent
Catalog No. T39000Cas No. 1513852-12-4
Alias ISC27864
Zaloglanstat (ISC-27864) is a selective, orally active mPGES-1 inhibitor with an IC50 of 5 nM against human mPGES-1, demonstrating analgesic effects in osteoarthritis and inflammatory arthritis.
Zaloglanstat
🥰Excellent
Purity: 99.97%
Catalog No. T39000Alias ISC27864Cas No. 1513852-12-4
Zaloglanstat (ISC-27864) is a selective, orally active mPGES-1 inhibitor with an IC50 of 5 nM against human mPGES-1, demonstrating analgesic effects in osteoarthritis and inflammatory arthritis.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $165 | - | In Stock | |
| 5 mg | $413 | - | In Stock | |
| 10 mg | $689 | - | In Stock | |
| 25 mg | $1,450 | - | In Stock | |
| 50 mg | $1,960 | - | In Stock | |
| 100 mg | $2,630 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $455 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.97%
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Product Introduction
Bioactivity
Chemical Properties
| Description | Zaloglanstat (ISC-27864) is a selective, orally active mPGES-1 inhibitor with an IC50 of 5 nM against human mPGES-1, demonstrating analgesic effects in osteoarthritis and inflammatory arthritis. |
| In vitro | Zaloglanstat exhibits selective inhibitory effects on both recombinant mPGES-1 activity and IL-1β in A549 cells, with IC50 values of 5 nM for both, while showing no significant inhibition on COX-1 and COX-2 (IC₅₀ >10 μM) [1]. In IL-1β-induced A549 cell and Homo sapiens synovial fibroblast models, Zaloglanstat can dose-dependently inhibit PGE₂ release, with an IC₅₀ value below 10 nM [1]. |
| Synonyms | ISC27864 |
| Molecular Weight | 452.86 |
| Formula | C21H20ClF3N4O2 |
| Cas No. | 1513852-12-4 |
| Smiles | CC(C)(C)C(=O)NCc1ccc(Cl)c(c1)-c1nn(-c2ccc(cc2)C(F)(F)F)c(=O)[nH]1 |
| Color | White |
| Appearance | Solid |
Storage & Solubility Information
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 200 mg/mL (441.64 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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Calculator
In Vivo Formulation Calculator (Clear solution)
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:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/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 μLSaline/PBS/ddH2O 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 μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
Dose Conversion
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Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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