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Arcyriaflavin A

CDK4/cyclin D1 inhibitor
ALX-350-375-M001 1 mg 218.00 USD
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Potent inhibitor of CDK4 / cyclin D1 (IC50 = 59nM). Inhibits human cytomegalovirus (HCMV) replication in cell culture (IC50 = 200nM).

Product Specification

Source:Synthetic. Originally isolated from the marine ascidian Eudistoma sp.
Purity:≥95% (HPLC)
Appearance:Orange to red solid.
Solubility:Soluble in DMSO (50mg/ml).
Long Term Storage:-20°C
Use/Stability:Stock solutions are stable for up to 3 months at -20°C.
Handling:Protect from light. Packaged under inert gas. After reconstitution, prepare aliquots and store at -20°C.
Regulatory Status:RUO - Research Use Only
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Product Literature References

Two indolocarbazole alkaloids with apoptosis activity from a marine-derived actinomycete Z(2)039-2: R. Liu, et al.; Arch. Pharm. Res. 30, 270 (2007), Abstract;
Aryl[a]pyrrolo[3,4-c]carbazoles as selective cyclin D1-CDK4 inhibitors: C. Sanchez-Martinez, et al.; Bioorg. Med. Chem. Lett. 13, 3835 (2003), Abstract;
Synthesis of quinolinyl/isoquinolinyl[a]pyrrolo [3,4-c] carbazoles as cyclin D1/CDK4 inhibitors: G. Zhu, et al.; Bioorg. Med. Chem. Lett. 13, 1231 (2003), Abstract;
Indolocarbazoles: potent, selective inhibitors of human cytomegalovirus replication: M.J. Slater, et al.; Bioorg. Med. Chem. 7, 1067 (1999), Abstract;
Staurosporine aglycone (K252-c) and arcyriaflavin A from the marine ascidian, Eudistoma sp: P.A. Horton, et al.; Experientia 50, 843 (1994), Abstract;

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