Docetaxel target prodrug and application thereof on preventing colorectal carcinoma
A doene taxane and colon cancer technology, applied in the field of biomedicine, can solve the problems of poor selectivity of cytotoxic small molecule compounds, high systemic toxicity, and expanded application, and achieve good anti-colon cancer potential and good anti-colon cancer activity , high biocompatibility effect
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Embodiment 1
[0025] Example 1: Preparation of docetaxel or tetrafluorodcetaxel coupled with colon cancer targeting polypeptide A1-A5 prodrug via bridging group Leu-PABOH(a)
[0026] Taxane targeting prodrugs were prepared by coupling paclitaxel (DTX) or tetrafluorodcetaxel (4FDT) with colon cancer targeting polypeptides A1-A5, and the synthetic route was as follows: figure 1 shown, including the following steps:
[0027] 1) Synthesis and activation modification of bridging group Leu-PABOH
[0028]
[0029]References (Elsadek B, Graeser R, Esser N, et al. Development of a novelprodrug of paclitaxel that is cleaved by prostate-specific antigen: An invitro and in vivo evaluation study [J]. European Journal of Cancer, 2010, 46( 18): The method adopted in 3434-3444) completes the synthesis and activation modification of the bridging group Leu-PABOH through a two-step reaction. That is: in a 25mL single-necked bottle, add 1mmol of Fmoc-L-Leu (1), 2mmol of p-aminobenzyl alcohol (PABOH) and 2...
Embodiment 2
[0070] Example 2: Proliferation inhibitory activity of targeted anti-colon cancer prodrugs on human colon cancer cell lines HCT116 and SW620 in vitro and toxicity evaluation on normal colon cell line CCD18Co and kidney cell line HEK293
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