Description
CC-671 is a dual TTK/CLK2 inhibitor. It acts by inhibiting the phosphorylation of KNL1 and SRp75, direct substrates of TTK and CLK2. It is a monotherapy candidate for treatment of triple negative breast cancer.
| Product Unit Size | Cost | Quantity | Stock |
|---|
CC-671 is a dual TTK/CLK2 inhibitor. It acts by inhibiting the phosphorylation of KNL1 and SRp75, direct substrates of TTK and CLK2. It is a monotherapy candidate for treatment of triple negative breast cancer.
| Cas No. | 1618658-88-0 |
|---|---|
| Purity | ≥98% |
| Formula | C28H28N6O4 |
| Formula Wt. | 512.57 |
| IUPAC Name | 4-{[4-(Cyclopentyloxy)-5-(2-methyl-1,3-benzoxazol-6-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl]amino}-3-methoxy-N-methylbenzamide |
| Synonym | CC 671, CC671 |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Riggs J., Nagy M., et al. The Discovery of a Dual TTK Protein Kinase/CDC2-Like Kinase (CLK2) Inhibitor for the Treatment of Triple Negative Breast Cancer Initiated from a Phenotypic Screen. J Med Chem. 60(21):8989-9002 (2017). PMID: 28991472.
Zhu D., Xu S., et al. Synthetic Lethal Strategy Identifies a Potent and Selective TTK and CLK1/2 Inhibitor for Treatment of Triple-Negative Breast Cancer with a Compromised G1-S Checkpoint. Mol Cancer Ther. 17(8):1727-38 (2018). PMID: 29866747.
Flavonolignan mixture found in Silybum (milk th...
Impurity of diclofenac
Benzothiazole; TRPC5 agonist, PTR1 inhibitor, v...
Prenylated phenolic terpene found in various pl...
NSAID; COX-1/2 inhibitor.
Mycotoxin.
ALK and Ros1 inhibitor, Trk antagonist.
Kavalactone originally found in Piper methystic...
Carbapenem β-lactam; penicillin binding protei...
Endogenous peptide hormone fragment, involved i...
Curcumin derivative; DNMT1 and α-amylase inhib...
Fermentation impurity
Essential fatty acid found in fish oil, involve...
Alkylphenol found in Ginkgo; HIV protease inhib...
Endogenous peptide hormone inolved in gastric e...
Laminin-derived hexapeptide.
Furocoumarin; voltage-gated Na+ channel blocker...
PDE3 inhibitor.
EphB4 inhibitor.