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KI-CDK9d-32

Chemical Structure : KI-CDK9d-32

CAS No.:

KI-CDK9d-32 (CDK9 PROTAC)

Catalog No.: PC-22535Not For Human Use, Lab Use Only.

KI-CDK9d-32 is a highly potent and selective CDK9 degrader with DC50 of 0.89 nM in MOLT-4 cells (4h) and Dmax of 97.7%, induces rapid reduction of MYC protein levels.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

KI-CDK9d-32 is a highly potent and selective CDK9 degrader with DC50 of 0.89 nM in MOLT-4 cells (4h) and Dmax of 97.7%, induces rapid reduction of MYC protein levels.
KI-CDK9d-32 significantly suppresses transcription of MYC in both a dose- and time dependent manner.
KI-CDK9d-32 represses canonical MYC pathways and leads to a destabilization of nucleolar homeostasis.
KI-CDK9d-32 has strong cytotoxic effects relative to the inhibitors used, but activity is limited in cells with high ABCB1 level.

Physicochemical Properties

M.Wt 703.85
Formula C39H45N9O4
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

4-((4-(2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)piperazin-1-yl)methyl)-N-((1R,3R)-3-((5-propylpyrazolo[1,5-a]pyrimidin-7-yl)amino)cyclopentyl)benzamide

References

1. Mohammed A Toure, et al. bioRxiv. 2024 May 15:2024.05.14.593352.

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