Conformation of cyclic heptapeptides: solid and solution state conformation of yunnanin A
β Scribed by Hiroshi Morita; Takashi Kayashita; Koichi Takeya; Hideji Itokawa; Motoo Shiro
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 737 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
The solid and solution state conformation of yunnanin A, a cyclic heptapeptide, cyclo(-Gly-Tyr-Gly-Gly-Pro-Phe-Pro-), isolated from the roots of Stellariu yunnanensis were studied. The X-ray diffraction studies showed that the crystal of yunnanin A [orthorhombic form from a ethanol-methanol mixture, a=1 1.754 (lo), b=12.576 (7), c=30.731 (6) A, space group P2221, 2=4] had three intramolecular hydrogen bonds forming one type II, one type II' p-turns, and a classical P-bulge unit with all tram amide bonds.
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## Abstract The solidβstate and solution conformations of (+)βchelidonine (1), a biologically active alkaloid, were determined by Xβray diffraction and ^1^HβNMR spectroscopy, XβRay diffraction analysis revealed a conformer with B/C β__anti__βtypeβ __cis__ conjunction, a halfβchair of ring B, and a