CK-636, with the CAS number 442632-72-6, is a small molecule that has garnered attention in the field of medicinal chemistry, particularly for its role as a selective inhibitor of the protein kinase CK2. This compound is characterized by its ability to modulate cellular signaling pathways, which can have implications in cancer research and treatment. CK-636 exhibits a specific binding affinity for CK2, thereby interfering with its activity and potentially leading to altered cell proliferation and survival. The chemical structure of CK-636 includes functional groups that contribute to its biological activity and selectivity. In vitro studies have demonstrated its effectiveness in inhibiting CK2-mediated phosphorylation, making it a valuable tool for investigating the role of CK2 in various cellular processes. Additionally, ongoing research is focused on understanding its pharmacokinetics, toxicity, and therapeutic potential in clinical settings. Overall, CK-636 represents a promising candidate for further exploration in the development of targeted therapies against diseases associated with dysregulated CK2 activity.

CK-636

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N-(2-(2-Methyl-1H-Indol-3-Yl)Ethyl)Thiophene-2-Carboxamide

CK-636 (CK-0944636), an Arp2/3 complex inhibitor, can inhibit actin polymerization induced by the human, fission yeast and bovine Arp2/3 complex.

CAS 442632-72-6: CK-636

CK-636

Ref: 54-BUP10195

CK-636

Ref: IN-DA00DB5H

N-(2-(2-Methyl-1H-Indol-3-Yl)Ethyl)Thiophene-2-Carboxamide

Ref: 54-OR1013939

CK-636

Ref: 7W-GL0805

CK-636

Ref: 10-F468327

CK-636

Ref: TM-T1820