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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

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 SizePriceAvailabilityQuantity
10 mgInquiry10-14 weeks
50 mgInquiry10-14 weeks
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Product Introduction

Bioactivity
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
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.
Chemical Properties
Molecular Weight443.34
FormulaC21H23BrN4O2
Cas No.2982787-50-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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