FTO-IN-3 CAS No.: 2585198-87-2

FTO-IN-3 CAS No.: 2585198-87-2 is a highly effective and advanced inhibitor that is used in cancer research. It inhibits the activity of fTO Kinase, which is involved in many signaling pathways linked to cancer progression.

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1. High Purity: FTO-IN-3 CAS No.: 2585198-87-2 has a high purity of at least 98%, making it suitable for use in a wide range of applications. The purity is verified using several analytical techniques, ensuring that the product is of the highest quality.

2. Potency: FTO-IN-3 CAS No.: 2585198-87-2 is extremely potent and has been shown to inhibit the activity of FTO Kinase, which is involved in the progression of various types of cancer. Its potency makes it an excellent choice for researchers looking to develop new cancer treatments.

3. Stability: FTO-IN-3 CAS No.: 2585198-87-2 is stable under a wide range of conditions, making it easy to handle and store. This ensures that the product remains effective for longer and reduces the need for frequent replacements.

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5. Easy to use: Our FTO-IN-3 CAS No.: 2585198-87-2 is easy to use and can be dissolved in a variety of solvents, making it highly versatile. This feature makes it suitable for use in a wide range of research applications.

Conclusion:

FTO-IN-3 CAS No: 2585198-87-2 is an excellent choice for merchants looking for a highly effective and cost-effective inhibitor for cancer research. Its high purity, potency, stability, and ease of use make it a highly attractive product for researchers looking to develop new cancer treatments. Our competitive pricing and commitment to quality make us the ideal choice for merchants looking for reliable sources of FTO-IN-3 CAS No.: 2585198-87-2. We guarantee that our product will meet your needs, and we look forward to partnering with you to drive innovation in cancer research.

Chemical Structure : FTO-04

CAS No.: 2585198-87-2

 

FTO-04

Catalog No.: URK-V609  Only Used For Lab.

FTO-04 is a potent, selective, competitive small molecule inhibitor of m6A-RNA demethylase FTO with IC50 of 3.39 uM, 13-fold selectivity over RNA demethylase ALKBH5 (ALKBH5, IC50=39.4 uM).
FTO-04 prevented neurosphere formation in patient-derived glioblastoma stem cells (GSCs) without inhibiting the growth of healthy neural stem cell-derived neurospheres.
FTO-04 increased m6A and m6Am levels in GSCs consistent with FTO inhibition.

Biological Activity

CM-272 (CM272) is a novel potent, selective and reversible dual inhibitor of G9a/DNMTs with IC50 of 8 nM and 382 nM for G9a and DNMT1, respectively; also inhibits DNMT3A/3B/GLP with IC50 of 85/1,200/2 nM, respectively; inhibits cell proliferation and promotes apoptosis in different haematological neoplasias (AML, ALL and DLBCL); significantly prolongs survival of AML, ALL and DLBCL xenogeneic models..

Physicochemical Properties

References

1. Sarah Huff, et al. ACS Chem Biol. 2021 Feb 19;16(2):324-333.

URK-V609_COA

URK-V609_SDS

URK-V609_TDS

 

Note: All products of Ureiko are only used for scientific research or drug certificate declaration, and we do not provide products and services for any personal use!

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