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CYC065

Chemical Structure : CYC065

CAS No.: 1070790-89-4

CYC065 (Fadraciclib, CYC-065)

Catalog No.: PC-61248Not For Human Use, Lab Use Only.

CYC065 (Fadraciclib) is a derivative of seliciclib and second generation CDK inhibitor that is mainly active on CDK2/5/9.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

CYC065 (Fadraciclib) is a derivative of seliciclib and second generation CDK inhibitor that is mainly active on CDK2/5/9.
CYC065 demonstrates cytotoxicity both in MM cell lines sensitive as well as resistant to conventional chemotherapy with IC50 of 0.06-2 uM.
CYC065 blocks cells in the G1 phase and inhibits cell growth specifically in CCNE1-overexpressing USCs.
CYC065 significantly reduces tumour growth in xenografts derived from CCNE1-amplified USCs.
CYC065 shows synergistic effect in vitro and in vivo combined with Taselisib.

Physicochemical Properties

M.Wt 397.527
Formula C21H31N7O
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

DMSO: 100 mg/mL

Chemical Name/SMILES

(2R,3S)-3-[[6-[(4,6-dimethylpyridin-3-yl)methylamino]-9-propan-2-ylpurin-2-yl]amino]pentan-2-ol

References

1. Cocco E, et al. Br J Cancer. 2016 Jul 26;115(3):303-11.

2. Kawakami M, et al. J Natl Cancer Inst. 2017 Jun 1;109(6).

3. Thomas AL, et al. Cell Cycle. 2017 Aug 3;16(15):1453-1464.

4. Rao SS, et al. Oncotarget. 2017 Aug 10;8(48):83925-83939.

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