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LSD1/HDAC6-IN-2
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Catalog No. T89134Cas No. 2982787-50-6
LSD1/HDAC6-IN-2 (JBI-802) is an orally effective inhibitor targeting LSD1, HDAC6, and MAO-A, demonstrating IC50 values of 5 nM, 11 nM, and 5 nM, respectively. This compound effectively suppresses the growth of multiple myeloma cells, including MM.1S, MM.1R, and RPMI-8226. Additionally, LSD1/HDAC6-IN-2 is utilized for researching acute myeloid leukemia and lymphoma.
LSD1/HDAC6-IN-2
😃Good
Catalog No. T89134Cas No. 2982787-50-6
LSD1/HDAC6-IN-2 (JBI-802) is an orally effective inhibitor targeting LSD1, HDAC6, and MAO-A, demonstrating IC50 values of 5 nM, 11 nM, and 5 nM, respectively. This compound effectively suppresses the growth of multiple myeloma cells, including MM.1S, MM.1R, and RPMI-8226. Additionally, LSD1/HDAC6-IN-2 is utilized for researching acute myeloid leukemia and lymphoma.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 25 mg | $1,930 | 10-14 weeks | |
| 50 mg | $2,610 | 10-14 weeks | |
| 100 mg | $3,330 | 10-14 weeks |
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Chemical Properties
| Description | LSD1/HDAC6-IN-2 (JBI-802) is an orally effective inhibitor targeting LSD1, HDAC6, and MAO-A, demonstrating IC50 values of 5 nM, 11 nM, and 5 nM, respectively. This compound effectively suppresses the growth of multiple myeloma cells, including MM.1S, MM.1R, and RPMI-8226. Additionally, LSD1/HDAC6-IN-2 is utilized for researching acute myeloid leukemia and lymphoma. |
| Targets&IC50 | MAO-B:6600 nM, HDAC6:11 nM, MAO-A:5 nM, LSD1:5 nM |
| In vitro | LSD1/HDAC6-IN-2 (JBI-802) exhibits growth inhibitory activity against multiple myeloma cells MM.1S, MM.1R, and RPMI-8226, with EC50 values of 2 nM, 6 nM, and 280 nM, respectively. |
| In vivo | LSD1/HDAC6-IN-2 (JBI-802), administered orally at a dosage of 25 mg/kg once daily for 12 days, exhibits antitumor activity in a mouse model of multiple myeloma. |
| Molecular Weight | 443.34 |
| Formula | C21H23BrN4O2 |
| Cas No. | 2982787-50-6 |
| Color | White |
| Appearance | Solid |
Storage & Solubility Information
| Storage | keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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.
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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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