HDAC6-IN-81
HDAC6-IN-81 is a potent selective HDAC6 inhibitor with an IC50 of 1 nM. HDAC6-IN-81 exhibits selectivity over class I HDAC isoforms (HDAC1/2/3/8). HDAC6-IN-81 can be used for the research of cancer.
Para uso exclusivo en investigación. No vendemos a pacientes.
- Fòrmula: C30H33N5O6
- Peso molecular:559.61
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Almacenamiento:
Please store the product under the recommended conditions in the Certificate of Analysis.
Actividad biológica
Descripciòn
IC50 & Target
[1]|
HDAC1 20 nM (IC50) |
HDAC6 1 nM (IC50) |
In Vitro
HDAC6-IN-81 (compound 18) (10 μM) potently inhibits purified HDAC1 (IC50 = 20 nM) and HDAC6 (IC50 = 1 nM) with a 20-fold preferential activity for HDAC6 over HDAC1[1].
HDAC6-IN-81 (10 nM) preferentially inhibits purified HDAC6 (81% inhibition) over purified class I HDAC isoforms HDAC1 (33% inhibition), HDAC2 (34% inhibition), HDAC3 (50% inhibition), and HDAC8 (4% inhibition)[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
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Peso molecular 559.61
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Fòrmula C30H33N5O6
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SMILES
O=C(NC1=CC=C(N(CCCCCC(NO)=O)C=C2C(NC3=CC=C(OC)C=C3)=O)C2=C1)NC4=CC=C(OC)C=C4
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Envío
Room temperature in continental US; may vary elsewhere.
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Almacenamiento
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocolo
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
Pureza y Documentación
Referencias
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)