FJ-5002 is a telomerase inhibitor with an IC50 of 2 µM. FJ-5002 can induce telomere shortening, increased chromosomal abnormalities, and senescence/crisis-like features in the human leukemia cell line U937. FJ-5002 exhibits antitumor activity and can be used in the study of cancer[1][2].
Molecular Weight:
452.06
CAS Number:
[247129-77-7]
Formula:
C20H22ClN3OS3
Target:
Telomerase
Application Notes:
MCE Product type: Reference compound
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