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PROTAC RIPK degrader-6 (example 1) is a PROTAC engineered for RIP Kinase degradation, comprising a RIP2 kinase inhibitor linked to a cereblon binder[1].
Pack Size | Price | Availability | Quantity |
---|---|---|---|
5 mg | $481 | Backorder | |
10 mg | $698 | Backorder | |
25 mg | $1,280 | Backorder | |
1 mL x 10 mM (in DMSO) | $770 | Backorder |
Description | PROTAC RIPK degrader-6 (example 1) is a PROTAC engineered for RIP Kinase degradation, comprising a RIP2 kinase inhibitor linked to a cereblon binder[1]. |
In vitro | PROTACs facilitate the targeted degradation of proteins and polypeptides by binding to cereblon at one end and the target protein (RIP2 kinase) at the other, thereby bringing the target protein close to the E3-Ligase. This interaction forms a ternary complex that results in the polyubiquitination and subsequent degradation of the target protein[1]. |
Molecular Weight | 889.01 |
Formula | C43H48N6O11S2 |
Cas No. | 2089205-64-9 |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
Solubility Information | DMSO: 100 mg/mL (112.49 mM) | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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