Comparison

Ryuvidine European Partner

Item no. HY-100624-1ea
Manufacturer MedChem Express
CASRN 265312-55-8
Amount 1 ea
Quantity options 100 mg 1 ea 1 mg
Category
Type Chemicals
Specific against other
Purity 99.40
Formula C15H12N2O2S
Citations [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.
[2]Blum G, et al. Small-molecule inhibitors of SETD8 with cellular activity. ACS Chem Biol. 2014 Nov 21;9(11):2471-8.
Smiles O=C1C=C(C(C2=C1SC(C)=N2)=O)NC3=CC=C(C)C=C3
ECLASS 10.1 32160000
ECLASS 11.0 32160000
UNSPSC 12000000
Available
Product Description
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[1]. Ryuvidine also inhibits CDK4 with an IC50 of 6.0 μM and is cytotoxic against a range of human cancer cells[2].
StorageTemperature
-20°C, 3 years; 4°C, 2 years (Powder)
Shipping
Room Temperature
Manufacturers Applications
Cancer-Kinase/protease
MolecularWeight
284.33
Clinical Information
No Development Reported
Manufacturers Research Area
Cancer
Solubility
DMSO : 12.5 mg/mL (ultrasonic; warming; heat to 60°C)
Target
CDK
Manufacturers Target
CDK
Isoform
CDK4
Manufacturers Pathway
Cell Cycle/DNA Damage
Manufacturers Product type
Reference compound

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 1 ea
Available: In stock
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