SS-208 |
Inhibitor of HDAC6
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| HDAC6 |
|
|
Inhibitor
up to 5 uM
Selectivity
In Vitro Selectivity Assessment
Potency: IC50 - HDAC1 1390 nM
Potency Assay Off-Target:
HDAC inhibition assay
Selectivity Assessment Description:
Selectivity against other HDAC isoforms (IC50, uM): HDAC4 (19.5), HDAC5 (6.91), HDAC7 (8.34), HDA ...
Potency Cellular
In Vitro
HDAC6
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? No
DOI Reference: 10.1021/acs.jmedchem.9b00946
In Vivo Validations
Chemical Information
| Molecular Formula | C13H11Cl2N3O4 |
| SMILEs | O=C(NCCc1cc(C(=O)NO)no1)c1ccc(Cl)c(Cl)c1 |
| InChI | InChI=1S/C13H11Cl2N3O4/c14-9-2-1-7(5-10(9)15)12(19)16-4-3-8-6-11(18-22-8)13(20)17-21/h1-2,5-6,21H,3-4H2,(H,16,19)(H,17,20) |
| Molecular weight | 343.01 Da |
| AlogP | 2.0728999999999997 |
| HBond acceptors | 7 |
| HBond donors | 3 |
| Atoms | 33 |
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