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Platelet Adhesion and Aggregation Under Flow using Microfluidic Flow Cells
Published on: October 27, 2009
Amides with anti-platelet aggregation activity from Piper taiwanense
Ih-Sheng Chen1, Yu-Chang Chen, Chang-Hui Liao
1Graduate Institute of Pharmaceutical Sciences, College of Pharmacy, Kaohsiung Medical University, Kaohsiung, Taiwan, ROC. m635013@kmu.edu.tw
Fitoterapia
|June 26, 2007
Summary
Piper taiwanense yielded five amides, including novel taiwanamides A-C. These compounds demonstrated significant potential in inhibiting platelet aggregation, with Taiwanamide C showing the most potent activity.
Area of Science:
- Natural Products Chemistry
- Pharmacology
- Medicinal Chemistry
Background:
- Piper species are a rich source of bioactive natural products.
- Amides are a class of compounds with diverse biological activities.
- Platelet aggregation plays a crucial role in thrombosis and hemostasis.
Purpose of the Study:
- To isolate and characterize new amide compounds from Piper taiwanense.
- To evaluate the in vitro inhibitory activity of isolated amides on platelet aggregation.
Main Methods:
- Isolation of compounds using chromatographic techniques.
- Structure elucidation of new amides employing spectral analyses (NMR, MS).
- In vitro platelet aggregation assays using collagen as an inducer.
Main Results:
- Three new amides, taiwanamides A-C (1-3), were isolated along with two known amides (4-5).
- All five isolated amides exhibited inhibitory effects on platelet aggregation.
- Taiwanamide C (3) demonstrated the most potent inhibition with an IC50 value of 8.9 microM.
- Taiwanamide B (2) and compound 5 showed IC50 values of 17.3 and 17.4 microM, respectively.
Conclusions:
- Piper taiwanense is a source of novel amide compounds with antiplatelet activity.
- Taiwanamide C is a promising lead compound for further investigation in the development of antiplatelet agents.
- The isolated amides contribute to the understanding of the chemical diversity and pharmacological potential of Piper species.

