Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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R275642-1mg | 1mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $33.90 | |
R275642-5mg | 5mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $129.90 | |
R275642-10mg | 10mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $199.90 | |
R275642-25mg | 25mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $448.90 | |
R275642-50mg | 50mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $809.90 |
SETD8 inhibitor; also CDK4 inhibitor
Synonyms | Cdk4 Inhibitor III | 5-(N-(4-Methylphenyl)amino)-2-methyl-4,7-dioxobenzothiazole | Ryuvidine |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | Ryuvidine is a potent inhibitor of SET domain-containing protein 8(SETD8) with an IC50 of 0.5 µM and suppresses monomethylation of H4K20 in vitro. Ryuvidine also inhibits CDK4 with an IC50 of 6.0 μM and is cytotoxic against a range of human cancer cells. |
Storage Temp | Protected from light,Store at -20°C,Argon charged |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of cyclin dependent kinase 2;Inhibitor of cyclin dependent kinase 4;Inhibitor of lysine methyltransferase 5A |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | 2-methyl-5-(4-methylanilino)-1,3-benzothiazole-4,7-dione |
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INCHI | InChI=1S/C15H12N2O2S/c1-8-3-5-10(6-4-8)17-11-7-12(18)15-13(14(11)19)16-9(2)20-15/h3-7,17H,1-2H3 |
InChi Key | HFPLHASLIOXVGS-UHFFFAOYSA-N |
Canonical SMILES | CC1=CC=C(C=C1)NC2=CC(=O)C3=C(C2=O)N=C(S3)C |
Isomeric SMILES | CC1=CC=C(C=C1)NC2=CC(=O)C3=C(C2=O)N=C(S3)C |
PubChem CID | 481747 |
Molecular Weight | 284.33 |
PubChem CID | 481747 |
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ChEMBL Ligand | CHEMBL290904 |
CAS Registry No. | 265312-55-8 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
B2421211 | Certificate of Analysis | Dec 10, 2024 | R275642 |
B2421378 | Certificate of Analysis | Dec 10, 2024 | R275642 |
B2421379 | Certificate of Analysis | Dec 10, 2024 | R275642 |
B2421380 | Certificate of Analysis | Dec 10, 2024 | R275642 |
B2421388 | Certificate of Analysis | Dec 10, 2024 | R275642 |
B2421210 | Certificate of Analysis | Jan 30, 2024 | R275642 |
B2421377 | Certificate of Analysis | Jan 30, 2024 | R275642 |
B2421381 | Certificate of Analysis | Jan 30, 2024 | R275642 |
B2421387 | Certificate of Analysis | Jan 30, 2024 | R275642 |
B2421620 | Certificate of Analysis | Jan 30, 2024 | R275642 |
Solubility | DMF: 5 mg/ml,DMF:PBS (pH 7.2) (1:4): 0.2 mg/ml,DMSO: 2 mg/ml,Ethanol: 0.5 mg/ml |
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Sensitivity | air sensitive;light sensitive |
Starting at $14.90
Starting at $23.90
Starting at $9.90
1. Ryu CK, Kang HY, Lee SK, Nam KA, Hong CY, Ko WG, Lee BH. (2000) 5-Arylamino-2-methyl-4,7-dioxobenzothiazoles as inhibitors of cyclin-dependent kinase 4 and cytotoxic agents.. Bioorg Med Chem Lett, 10 (5): (461-4). [PMID:10743948] [10.1021/op500134e] |
2. Houston SI, McManus KJ, Adams MM, Sims JK, Carpenter PB, Hendzel MJ, Rice JC. (2008) Catalytic function of the PR-Set7 histone H4 lysine 20 monomethyltransferase is essential for mitotic entry and genomic stability.. J Biol Chem, 283 (28): (19478-88). [PMID:18480059] [10.1021/op500134e] |
3. Blum G, Ibáñez G, Rao X, Shum D, Radu C, Djaballah H, Rice JC, Luo M. (2014) Small-molecule inhibitors of SETD8 with cellular activity.. ACS Chem Biol, 9 (11): (2471-8). [PMID:25137013] [10.1021/op500134e] |
4. Jorda R, Hendrychová D, Voller J, Řezníčková E, Gucký T, Kryštof V. (2018) How Selective Are Pharmacological Inhibitors of Cell-Cycle-Regulating Cyclin-Dependent Kinases?. J Med Chem, 61 (20): (9105-9120). [PMID:30234987] [10.1021/op500134e] |