AN-7
AN-7 is an orally active histone deacetylase (HDAC) inhibitor that induces histone hyperacetylation and differentiation in vitro and in vivo, and inhibits the proliferation of human prostate 22Rv1 cancer cells. AN-7 can increase the expression of the pro-apoptotic protein Bax, reduce the expression of the anti-apoptotic protein Bcl-2, and promote apoptosis by activating caspase-3, and can be used in the study of prostate cancer.
For research use only. We do not sell to patients.
- CAS No.: 213262-83-0
- Formula: C9H19O6P
- Molecular Weight:254.22
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biological Activity
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Chemical Information
- Purity & Documentation
- References
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Help & FAQs
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Biological Activity
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| U-251 | IC50 |
89 μM
Compound: 12
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Cytotoxicity against human U251 cells after 72 hrs by Hoechst test
Cytotoxicity against human U251 cells after 72 hrs by Hoechst test
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[PMID: 19007111] |
Chemical Information
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CAS No. 213262-83-0
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Molecular Weight 254.22
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Formula C9H19O6P
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SMILES
CCCC(OCOP(OCC)(OCC)=O)=O
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
AN-7 Related Classifications
HY-117136 Related Classifications
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