[1]谭宁华, 周俊, 赵守训. 植物环肽研究进展[J]. 药学学报, 1997, 32(5): 388-399.[2]纪建国, 叶蕴华, 刑其毅. 植物多肽类化合物研究进展[J]. 天然产物研究与开发, 1998, 10(3): 80-86.[3]沈晓羽, 吴厚铭, 何敏,等. 环肽配糖体的二维核磁共振谱研究[J]. 化学学报, 1996, 54:1194-1199.[4]翟纯. 全相关技术[J]. 波谱学杂志, 1992, 9(1): 59-65.[5]滕荣伟, 王德祖, 李朝明,等. HMQCTOCSY技术在植物环肽和配糖体中的应用[J]. 波谱学杂志, 1999, 16(4): 295-301.[6]Itokawa H, Morita H, Takeya K. Solution forms of an antitumor cyclic hexa peptide, RA-VII in dimethyl sulfoxided\-6 from nuclear magnetic resonance studies[J]. Chem Pharm Bull, 1992, 40(4): 1050-1052.[7]Itokawa H, Yamamiya T, Morita H, et al. New antitumor bicyclic hexapeptides, RA-IX and RA-X from Rubia cordifolia. part 3. conformation-antitumor activity relationship[J]. Chem Soc Perkin Trans I, 1992, 455-459.[8]Morita H, Yamamiya T, Takeya K, et al. conformational recognition of RA-XVII by 80s ribosomes: a differential line broadening study in 1H NMR spectroscopy[J]. Chem Pharm Bull, 1993, 41(4): 781-783.[9]Itokawa H, Morita H, Takeya K, et al. New antitumor bicyclic hexapeptides, RA-VI and-VIII from rubia cordifolia; Conformation-activity relationshipII[J]. Tetrahedron, 1991, 47(34): 7007-7020.[10]Morita H, Kondo K, Hitotsuyanagi Y, et al. Conformational analysis of antitumor cyclic hexapeptides, RA series[J]. Tetrahedron, 1991, 47(16/17): 2757-2772.[11]Shiomi K, Arai N, Iwai Y, et al. Structure of argifin, a new chitinase inhibitor produced by Gliocladium sp[J]. Tetrahedron letters, 2000, 41: 2141-2143.[12]Fujii K, Sivonen K, Naganawa E, et al. Non-Toxic Peptides from Toxic Cyanobacteria, Oscillatoria agardhii[J]. Tetrahedron, 2000, 56(6): 725-733.[13]Ding Z T, Zhou J, Tang N H, et al. Two new cyclic peptides from Drymaria diandra[J]. Planta Medica, 2000, 66: 386-388.[14]Mu Q, Teng R W, Li C M, et al. Leiocyclocin A and B, two cyclopeptides from Goniothalamus leiocarpus[J]. Chin Chem Lett, 2001, 12(7): 607-610.[15]龚运淮. 天然有机化合物的13C -1H核磁共振化学位移[M]. 昆明: 云南科学和科技出版社, 1986.449-455 |