SAHA chloroalkane T1
≥98%
- Product Code: 102453
CAS:
1613617-05-2
| Molecular Weight: | 719.26 g./mol | Molecular Formula: | C₃₃H₅₅ClN₄O₁₁ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
SAHA chloroalkane T1 is primarily utilized in the field of biomedical research, particularly in studies related to epigenetics and cancer therapy. It functions as a histone deacetylase (HDAC) inhibitor, which plays a crucial role in regulating gene expression by modifying chromatin structure. This chemical is often employed in experimental settings to investigate the mechanisms of gene silencing and to explore potential therapeutic strategies for treating various cancers. By inhibiting HDAC activity, it can reactivate tumor suppressor genes, leading to the suppression of tumor growth and the induction of apoptosis in cancer cells. Additionally, SAHA chloroalkane T1 is used in the development of targeted drug delivery systems, where its chloroalkane moiety can be exploited for specific interactions with cellular targets, enhancing the precision and efficacy of therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | $927.57 |
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| 0.010 | 10-20 days | $1,597.49 |
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SAHA chloroalkane T1
SAHA chloroalkane T1 is primarily utilized in the field of biomedical research, particularly in studies related to epigenetics and cancer therapy. It functions as a histone deacetylase (HDAC) inhibitor, which plays a crucial role in regulating gene expression by modifying chromatin structure. This chemical is often employed in experimental settings to investigate the mechanisms of gene silencing and to explore potential therapeutic strategies for treating various cancers. By inhibiting HDAC activity, it can reactivate tumor suppressor genes, leading to the suppression of tumor growth and the induction of apoptosis in cancer cells. Additionally, SAHA chloroalkane T1 is used in the development of targeted drug delivery systems, where its chloroalkane moiety can be exploited for specific interactions with cellular targets, enhancing the precision and efficacy of therapeutic agents.
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