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sEH/HDAC6-IN-2

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Catalog No. T88891Cas No. 3009011-58-6

sEH/HDAC6-IN-2 is an effective dual inhibitor of soluble epoxide hydrolase (sEH) and HDAC6, demonstrating IC50 values of 0.9 nM for human sEH, 46.8 nM for mouse sEH, and 8 nM for HDAC6. It is used in research focused on inflammatory pain.

sEH/HDAC6-IN-2

sEH/HDAC6-IN-2

😃Good
Catalog No. T88891Cas No. 3009011-58-6
sEH/HDAC6-IN-2 is an effective dual inhibitor of soluble epoxide hydrolase (sEH) and HDAC6, demonstrating IC50 values of 0.9 nM for human sEH, 46.8 nM for mouse sEH, and 8 nM for HDAC6. It is used in research focused on inflammatory pain.
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10 mgInquiry10-14 weeks
50 mgInquiry10-14 weeks
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Product Introduction

Bioactivity
Description
sEH/HDAC6-IN-2 is an effective dual inhibitor of soluble epoxide hydrolase (sEH) and HDAC6, demonstrating IC50 values of 0.9 nM for human sEH, 46.8 nM for mouse sEH, and 8 nM for HDAC6. It is used in research focused on inflammatory pain.
Targets&IC50
HDAC2:0.492 μM, HDAC1:1.151 μM, Human sEh:0.0009 μM, Mouse sEh:0.0468 μM, HDAC8:0.062 μM, HDAC6:0.008 μM, HDAC11:0.464 μM, HDAC3:1.276 μM
In vitro
sEH/HDAC6-IN-2 exhibits selective inhibition towards HDAC6, demonstrated by its significant selectivity indices (HDAC1/HDAC6 = 144, HDAC2/HDAC6 = 62, HDAC3/HDAC6 = 160, HDAC8/HDAC6 = 8, HDAC11/HDAC6 = 58). When administered at concentrations of 1-2 μM for 24 hours, sEH/HDAC6-IN-2 (compound 28g) induces an increase in acetylation of α-tubulin without affecting histone H3, indicating a selective inhibition of HDAC6.
In vivo
sEH/HDAC6-IN-2 (compound 28g; 30 mg/kg; intraperitoneal injection; single dose) alleviated inflammation-induced pain in mice following formalin exposure.
Chemical Properties
Molecular Weight580.02
FormulaC27H32ClF2N5O5
Cas No.3009011-58-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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