>>Signaling Pathways>> Cell Cycle/Checkpoint>> Microtubule/Tubulin>>Valecobulin (CKD-516)

Valecobulin (CKD-516) (Synonyms: CKD-516)

Catalog No.GC33269

발레코불린(CKD-516)(CKD516)은 (S516) 및 혈관 교란제(VDA)의 발린 전구약물이다. Valecobulin(CKD-516)은 β-튜불린 중합 억제제로 쥐 및 인간 고형 종양에 대해 현저한 항종양 활성을 보입니다.

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Valecobulin (CKD-516) Chemical Structure

Cas No.: 1188371-47-2

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Valecobulin (CKD516), a valine prodrug of (S516) and a vascular disrupting agent (VDA), is a potent beta-tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors[1][2].

The size change of the tumor in VX2 liver tumor-bearing rabbits is significantly smaller in the Valecobulin (CKD516)( 5, 9, or 12 mg/m2, i.v.)- treated group than in control group[2].|| Animal Model:|VX2 liver tumor-bearing rabbits (Male New Zealand White rabbits weighing between 2.5 and 3.5 kg)[2]. |Dosage:|Dissolved in 5 mL of saline at a dose of 5, 9, or 12 mg/m2 of body surface area.|Administration:|Intravenous injection once.|Result:|The size change of the tumors was significantly smaller in the treated group than in control group.

[1]. Lee J, et al. Identification of CKD-516: a potent tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors. J Med Chem. 2010 Sep 9;53(17):6337-54. [2]. Joo I, et al. Intravoxel incoherent motion diffusion-weighted MR imaging for monitoring the therapeutic efficacy of the vascular disrupting agent CKD-516 in rabbit VX2 liver tumors. Radiology. 2014 Aug;272(2):417-26.

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