Synthesis and biological evaluation of oleanolic acid analogs based on survivin target / 中国药学杂志

OBJECTIVE: To design and synthesize a series of oleanolic acid analogs posessing anti-tumor activity based on survivin target. METHODS: Using the techniques of computer-aided drug design, the docking of Survivin and known active small molecules was simulated and then the key amino acid residue fragment of the target protein was analyzed. It led to the discovery of active groups capable of binding to the critical sites. Through using the natural product, oleanolic acid, as a lead compound, the active groups were introduced onto its A-ring, and the carboxyl group at the C-28 position was modified using amidation. SGC-7901 and A549 cells were used to screen the antitumor activity in vitro through the standard MTT method. RESULTS: Ten new oleanolic acid derivatives were designed and synthesized,and their structures were confirmed by MS and NMR. The compounds 5 and Ⅱ5 exhibited more potent cytotoxicity than the positive control drugs. CONCLUSION: The novel oleanolic acid analogues have better antitumor activity than the parent compound, which are worthy of further study.

Targeting PDGF receptor inhibitors: synthesis and biological evaluation of oleanolic acid analogs / 药学学报

The computer-aided design was used to simulate the docking of PDGF receptor with known active compounds, and the active groups that can bind to key sites were identified by analyzing the key amino acid residue fragments that exerted active effects on the target proteins. The natural product oleanolic acid was used as the parent, and the active group was introduced into the 2-position, and the C-28 carboxyl group was esterified and amidated. A series of oleanolic acid analogues targeting PDGF receptor inhibitors were designed and synthesized. Their structures were confirmed by MS and NMR. Through MTT assay, SGC-7901 and A549 cells were selected for preliminary in vitro anti-tumor activity screening. PDGF receptor protein inhibition test was performed on I3 and Ⅱ5 by FPIA. The activity tests showed that I3 and Ⅱ5, compared with the positive control drug, had stronger inhibition. FPIA test showed that Ⅱ5 and PDGF receptor protein had good binding ability. The newly synthesized oleanolic acid analogues have significantly higher antitumor activity than the parent compound and deserve further study.

Studies on chemical constituents from Semiliquidambar cathayensis / 中草药

Object To isolate and identiified the chemical constituents from the EtOAc soluble fraction of the rhizome of Semiliquidambar cathayensis Chang with anti inflammatory activity Methods The EtOAc soluble fraction of anti inflammatory activity was determined on the basis of the mouse ear irritant assay by croton oil The chemical constituents were isolated by silica gel column chromatography, and their structures were identiified by IR, MS and NMR spectroscopic methods including HMQC and HMBC experiments Results Four oleanolic acid derivatives, oleanolic acid, 3 oxo olean 12 en 28 oic acid 2?, 3? dihydroxyolean 12 en 28 oic acid, 2?, 3?, 23 trihydroxyolean 12 en 28 oic acid (arjunolic acid); three ellagic acid derivatives, ellagic acid 3, 3′ dimethylether, ellagic acid 3, 3′, 4 trimethylether, and ellagic acid 4 O ? D xylopyranoside 3, 3′ dimethylether, together with ? sitosterol and octadecylic acid were obtained and identified Conclusion All the nine compounds were isolated for the first time from the title plant