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RO-275
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Catalog No. T87339Cas No. 2648837-04-9
RO-275 (compound 29), recognized for its potency and selectivity, acts as an orally active HCN1 inhibitor, exhibiting IC 50 values of 0.046 µM for HCN1, 14.3 µM for HCN2, 4.6 µM for HCN3, and 13.9 µM for HCN4. Notably, RO-275 enhances working memory, suggesting its research utility for cognitive impairments associated with brain disorders [1] [2].
RO-275
😃Good
Catalog No. T87339Cas No. 2648837-04-9
RO-275 (compound 29), recognized for its potency and selectivity, acts as an orally active HCN1 inhibitor, exhibiting IC 50 values of 0.046 µM for HCN1, 14.3 µM for HCN2, 4.6 µM for HCN3, and 13.9 µM for HCN4. Notably, RO-275 enhances working memory, suggesting its research utility for cognitive impairments associated with brain disorders [1] [2].
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 10 mg | Inquiry | 8-10 weeks | |
| 50 mg | Inquiry | 8-10 weeks |
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Product Introduction
Bioactivity
Chemical Properties
| Description | RO-275 (compound 29), recognized for its potency and selectivity, acts as an orally active HCN1 inhibitor, exhibiting IC 50 values of 0.046 µM for HCN1, 14.3 µM for HCN2, 4.6 µM for HCN3, and 13.9 µM for HCN4. Notably, RO-275 enhances working memory, suggesting its research utility for cognitive impairments associated with brain disorders [1] [2]. |
| In vivo | RO-275, administered intraperitoneally at doses of 3, 10, or 30 mg/kg, enhances working memory performance in male Sprague Dawley rats. At 10 mg/kg, it tended to improve results in a touchscreen task with a 6-second delay. At 30 mg/kg, it significantly reduced incorrect trials in a trial-unique, delayed non-matching-to-location (TUNL) assessment. |
| Molecular Weight | 351.79 |
| Formula | C18H14ClN5O |
| Cas No. | 2648837-04-9 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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:
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% 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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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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