265312-55-8
Chemical Structure
Ryuvidine
- CAS No.: 265312-55-8
- Formula:C15H12N2O2S
- Molecular Weight:284.33
IUPAC Name: 2-methyl-5-(p-tolylamino)benzo[d]thiazole-4,7-dione
InChIKey: HFPLHASLIOXVGS-UHFFFAOYSA-N
SMILES: O=C1C=C(C(C2=C1SC(C)=N2)=O)NC3=CC=C(C)C=C3
Biological Activity: Ryuvidine is a potent inhibitor of SET domain-containing protein 8(SETD8) with an IC50 of 0.5 µM and suppresses monomethylation of H4K20. Ryuvidine also inhibits CDK4 with an IC50 of 6.0 μM. Ryuvidine also inhibits KDM5A and blocks DNA synthesis. Ryuvidine has anticancer activity against tumors such as breast cancer. Ryuvidine improves arthritis[1][2][3][4][5].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Ryuvidine | 99.23% | Ryuvidine is a potent inhibitor of SET domain-containing protein 8(SETD8) with an IC50 of 0.5 µM and suppresses monomethylation of H4K20. Ryuvidine also inhibits CDK4 with an IC50 of 6.0 μM. Ryuvidine also inhibits KDM5A and blocks DNA synthesis. Ryuvidine has anticancer activity against tumors such as breast cancer. Ryuvidine improves arthritis. | ||||||||||||||||||||
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- [1]. Ryu CK, et al. 5-Arylamino-2-methyl-4,7-dioxobenzothiazoles as inhibitors of cyclin-dependent kinase 4 and cytotoxic agents. Bioorg Med Chem Lett. 2000 Mar 6;10(5):461-4. [Content Brief]
- [2]. Blum G, et al. Small-molecule inhibitors of SETD8 with cellular activity. ACS Chem Biol. 2014 Nov 21;9(11):2471-8. [Content Brief]
- [3]. FitzGerald J, et al. A high through-put screen for small molecules modulating MCM2 phosphorylation identifies Ryuvidine as an inducer of the DNA damage response. PLoS One. 2014 Jun 5;9(6):e98891. [Content Brief]
- [4]. Ali R, et al. Isolation and Establishment of a Highly Proliferative, Cancer Stem Cell-Like, and Naturally Immortalized Triple-Negative Breast Cancer Cell Line, KAIMRC2. Cells. 2021 May 24;10(6):1303. [Content Brief]
- [5]. Cotti S, et al. More bone with less minerals: the effects of dietary phosphorus on the zebrafish skeleton[C]//49th European Calcified Tissue Society Congress (ECTS 2022). 2022, 16: 59-60.
Keywords
