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SS-208

Catalog No. T16936   CAS 2245942-72-5

SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes.

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SS-208 Chemical Structure
SS-208, CAS 2245942-72-5
Pack Size Availability Price/USD Quantity
1 mg In stock $ 112.00
5 mg In stock $ 239.00
10 mg In stock $ 397.00
25 mg In stock $ 663.00
50 mg In stock $ 945.00
100 mg In stock $ 1,280.00
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Purity: 99.07%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes.
Targets&IC50 HDAC6:12 nM, HDAC8:1.23 μM, HDAC1:1.39 μM, HDAC11:5.12 μM, HDAC5:6.91 μM, HDAC7:8.34 μM
In vivo In C57BL/6 mice injected immunogenic murine SM1 melanoma cells, SS-208 (25 mg/kg; i.p.) causes a significant reduction of the tumor growth[1].
Molecular Weight 344.15
Formula C13H11Cl2N3O4
CAS No. 2245942-72-5

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 100 mg/mL (290.6 mM), Sonification is recommended.

TargetMolReferences and Literature

1. Shen S, et al. Discovery of a New Isoxazole-3-hydroxamate-Based Histone Deacetylase 6 Inhibitor SS-208 with Antitumor Activity in Syngeneic Melanoma Mouse Models. J Med Chem. 2019 Sep 4.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Active Compound Library Inhibitor Library NF-κB Signaling Compound Library Chromatin Modification Compound Library Anti-Cancer Compound Library Anti-Pancreatic Cancer Compound Library Histone Modification Compound Library Bioactive Compounds Library Max DNA Damage & Repair Compound Library Bioactive Compound Library

Related Products

Related compounds with same targets
BRD4097 7,4'-Dihydroxyflavone HDAC6-IN-21 Sulforaphane PRO-HD2 SW-100 BEBT-908 2-hexyl-4-Pentynoic Acid

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Keywords

SS-208 2245942-72-5 Chromatin/Epigenetic DNA Damage/DNA Repair HDAC SS 208 SS208 inhibitor inhibit

 

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