Coumarin-SAHA

Catalog No.: A26329
Fluorescent Probe
Coumarin-SAHA is a fluorescent probe designed to investigate the binding affinities (kd) and dissociation off-rates (koff) of histone deacetylase 8 (HDAC8) inhibitor complexes. This compound is particularly valuable in research applications focused on epigenetic regulation and cancer biology. The fluorescent properties of Coumarin-SAHA enable real-time monitoring of molecular interactions, enhancing the understanding of HDAC functions and their role in disease mechanisms.
Grouped product items
Size Price Stock Qty
1mg
$65.00
In stock
10mg
$405.00
In stock
25mg
$745.00
In stock
Bulk Size
Bulk Discount
Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionCoumarin-SAHA is a fluorescent probe designed to investigate the binding affinities (kd) and dissociation off-rates (koff) of histone deacetylase 8 (HDAC8) inhibitor complexes. This compound is particularly valuable in research applications focused on epigenetic regulation and cancer biology. The fluorescent properties of Coumarin-SAHA enable real-time monitoring of molecular interactions, enhancing the understanding of HDAC functions and their role in disease mechanisms.
Product Information
Catalog NumA26329
FormulaC18H22N2O5
Molecular Weight346.38
CAS Number1260635-77-5
SMILESO=C(NO)CCCCCCC(NC1=CC=C(C(O2)=C1)C(C)=CC2=O)=O
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