“…In a tube formation assay, 332 showed the most potent antiangiogenic activity in primary screening, and its IC 50 value was determined to be 40.4 µM [78]. In addition to VEGFR2, 332 decreased BMP4 expression, which regulates tube formation, and glycolysisrelated proteins, including GLUT1 and HK2, which suggests that the novel compound 332 is worthy of additional investigation for angiogenesis-associated pathological conditions [78]. Onopornoids A-D (334-337) (Figure 8), three elemanes and one germacrane, were extracted from the whole aerial parts of Onopordum alexandrinum, which possess unique structures combining a sesquiterpenoid framework with an amino acid, L-proline [79].…”