Recent advances in the study of natural homoisoflavonoids

Yaoxue Xuebao

Volumn 42, Issue 2, 2007, Pages 118-126

  Jiang, Hong Bo ^a   Huang, Jing ^a   Guo, Ming Juan ^a   Zou, Ping ^a   Tian, Xiang Qin ^a  

^a SICHUAN UNIVERSITY   (China)

Author keywords

Bioactivity; Homoisoflavonoids; NMR; Structure

Indexed keywords

ANTIINFLAMMATORY AGENT; ANTIMUTAGENIC AGENT; ANTINEOPLASTIC AGENT; ISOFLAVONE DERIVATIVE; VASODILATOR AGENT;

ANIMAL; ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; HUMAN; ISOLATION AND PURIFICATION; MEDICINAL PLANT; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

ANIMALS; ANTI-INFLAMMATORY AGENTS; ANTIMUTAGENIC AGENTS; ANTINEOPLASTIC AGENTS, PHYTOGENIC; HUMANS; ISOFLAVONES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; PLANTS, MEDICINAL; VASODILATOR AGENTS;

EID: 34247101774     PISSN: 05134870     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (54)

1. Liu CJ, Zeng Q, Ma B. Chemical constituents of dwarf lilyturf (Ophiopogon japonicus) [J]. Chin Tradit Herb Drugs, 1988,19:10-11.
2. Tang YP, Yu B, Hu J, et al. Three new homoisoflavanone glycosides from the bulbs of Ornithogalum caudatum [J]. J Nat Prod, 2002,65:218-220.
3. Akihiro T, Ryoji K, Tamotsu S, et al. Studies on the constituents of ophiopogonis tuber V. Isolation of a novel class of homoisoflavonoids and determination of their structures (1) [J]. Chem Pharm Bull, 1980,28:1477-1484.
4. Kim DS, Back NI, Oh SR, et al. NMR assignment of brazilein [J]. Phytochemistry, 1997,46:177-178.
5. Akihiro T, Ryoji K, Tamotsu S, et al. Studies on the constituents of ophiopogonis tuber VI. Structures of homoisoflavonoids. (2) [J]. Chem Pharm Bull, 1980,28:2039-2044.
6. Takayuki A, Tetsuya M, Yasuaki H, et al. Comparative studies on the constituents of ophiopogonis tuber and its congeners. VII [J]. Chem Pharm Bull, 1993,41:391-393.
7. Yoshiaki W, Shuichi S, Yoshiteru I, et al. Comparative studies on the constituents of ophiopogonis tuber and its congeners. IV [J]. Chem Pharm Bull, 1985,33:5385-5363.
8. Zhu YX, Yan KD, Tu GS. Isolation and identification of homoisoflavanones from Maidong (Ophiopogon japonicus (Thunb) Ker-Gawal) [J]. Acta Pharm Sin, 1987,22:679-684.
9. Chang JM, Shen CC, Huang YL, et al. Five new homoisoflavonoids from the tuber of Ophiopogon japonicus [J]. J Nat Prod, 2002,65:1731-1733.
10. Adinolfi M, Barone G, Lanzetta R, et al. Three 3-benzyl-4-chromanones from Muscari comosum [J]. Phytochemistry, 1985,24:624-626.
11. Jiang HB, Tian XQ, Hu XB, et al. The stero-structures of homoisoflavonoids from Ophiopogon japonicus [J/OL]. 2006, http://www.paper.edu.cn.
12. Norito K, Hiroyuki N, Tadayuri K, et al. Studies on the components of Ophiopogon roots [J]. Yakugaku Zasshi, 1983,103:1133-1139.
13. Hoang Anh NT, Van Sung T, Porzel A, et al. Homosioflavonoids from Ophiopogon japonicus Ker-Gawler [J]. Phytochemistry, 2003,62:1153-1158.
14. Sidwell WTL, Tamm C. Homo-isoflavones II. Isolation and structure of 4′-O-methyl-punctain, autumnalin and 3,9-dihydro-autumnalin [J]. Tetrahedron Lett, 1970,7:475-478.
15. Von WH, Paul A, Werner AS, et al. Homoisoflavanone. IV. Neue inhaltsstoffe der eucomin-reihe von eucomis bicolor [J]. Helv Chim Acta, 1976,59:2048-2058.
16. Koorbanally C, Mulholland DA, Crouch NR. A novel homoisoflavonoid from Drimia delagoensis (Urgineoideae: Hyacinthaceae) [J]. Biochem Syst Ecol, 2005,33:743-748.
17. Silayo A, Ngadjui BT, Abegaz BM. Homoisoflavonoids and stilbenes from the bulbs of Scilla nervosa subsp. rigidifolia [J]. Phytochemistry, 1999,52:947-955.
18. Amschler G, Frahm AW, Hatzelmann A, et al. Constituents of Veltheimia viridifolia. I. Homoisoflavanones of the bulbs [J]. Planta Med, 1996,62:534-540.
19. Mutanyatta J, Matapa BC, Shushu DD, et al. Homoisoflavonoids and xanthones from the tubers of wild and invitro regenerated Ledebouria graminifolia and cytotoxic activities of some of the homoisoflavonoids [J]. Phytochemistry, 2003,62:797-804.
20. Adinolfi M, Barone G, Belardini M, et al. Homoisoflavanones from Muscari comosum bulbs [J]. Phytochemistry, 1985,24:2423-2426.
21. Adinolfi M, Aquila T, Barone G, et al. Homoisoflavanones from Bellevalia romana [J]. Phytochemistry, 1989,28:3244-3246.
22. Jain SC, Sharma SK, Kumar R, et al. A homoisoflavanone from Pterocarpus marsupium [J]. Phytochemistry, 1997,44:765-766.
23. Vastano BC, Rafi MM, Dipaola RS, et al. Bioactive homoisoflavones from Vietnamese coriander or pak pai (Pofygonatum odoratum) [J]. ACS Symposium Series, 2002, 803 (Quality Management of Natraceuticals): 269-280.
24. Crouch NR, Bangani V, Mulholland DA. Homoisoflavanones from three South African Scilla species [J]. Phytochemistry, 1999,51:943-946.
25. Bangani V, Crouch NR, Mulholl DA, et al. A homoisoflavanones and stilbenoids from Scilla nervosa [J]. Phytochemistry, 1999,51:947-951.
26. Delazar A, Nazemiyeh H, Afshar J, et al. Identification of a new homoisoflavanone from Bellevalia longistyla [J]. Ulumi Daroei (Tabriz, Islamic Republic of Iran), 2002,1:33-38.
27. O'Donnell G, Bucar F, Gibbons S. Phytochemistry and antimycobacterial activity of Chlorophytum inornatum [J]. Phytochemistry, 2006,67:178-182.
28. Adinolfi M, Corsaro MM, Lanzetta R, et al. Ten homoisoflavanones from two Muscari species [J]. Phytochemistry, 1987,26:285-290.
29. Corsaro MM, Lanzetta R, Mancino A, et al. Homoisoflavanones from Chionodoxa luciliae [J]. Phytochemistry, 1992,31:1395-1397.
30. Mulholland DA, Crouch NR, Pohl TL, et al. A homoisoflavanone from Ornithogalum longibracteatum [J]. Biochem Syst Ecol, 2004,32:499-502.
31. Tamm C. Homoisoflavones, a new series of natural products [J]. Arzneimittel-forsch, 1972,22:1776-1784.
32. Likhitwitayawuid K, Sawasdee K, Kirtikara K. Flavonoids and stilbenoids with COX-1 and COX-2 inhibitory activity from Dracaena loureiri [J]. Planta Med, 2002,68:841-843.
33. Du TK, Elgorashi EE, Malan SF, et al. Anti-inflammatory activity and QSAR studies of compounds isolated from Hyacinthaceae species and Tachiadenus longiflorus Griseb. (Gentianaceae) [J]. Bioorg Med Chem, 2005,13:2561-2568.
34. Mcpherson DD, Cordell GA, Soejarto DD, et al. Peltogynoids and homoisoflavonoids from Caesalpinia pulcherrima [J]. Phytochemistry, 1983,22:2835-2838.
35. Wall ME, Wani MC, Manikumar G, et al. Plant antimutagens 6. Intricatin and intricatinol, new antimutagenic homoisoflavonoids from Hoffmanosseggia intricate [J]. J Nat Prod, 1989,52:774-778.
36. Purushothaman KK, Kalyani K, Subramaniam K, et al. Structure of bonducellin- a new homoisoflavone from Caesalpina bonducella [J]. Indian J Chem, Sect B: Org Chem Including Med Chem, 1982,21B:383.
37. Masterova I, Suchy V, Uhrin D, et al. Homoisoflavanones and other constituents from Muscari racemosum [J]. Phytochemistry, 1991,30:713-714.
38. Kouno I, Komori T, Kawasaki T. Structure of new types of homoisoflavanones from bulbs of Scilla scilloides [J]. Tetrahedron Lett, 1973,46:4569-4572.
39. Barone G, Corsaro MM, Lanzetta R, et al. Homoisoflavanones from Muscari neglectum [J]. Phytochemistry, 1988,27:921-923.
40. Xie YW, Ming DS, Xu HX, et al. Vasorelaxing effects of Caesalpinia sappan involvement of endogenous nitric oxide [J]. Life Sci, 2000,67:1913-1918.
41. Niranjan Reddy VL, Ravikanth V, Jansi Lakshmi VVNS, et al. Inhibitory activity of homoisoflavonoids from Caesalpinia sappan against Beauveria bassiana [J]. Fitoterapia, 2003,74:600-602.
42. Wang D, Chen C, Zhou Y. The survey of Caesalpinia sappan L. [J]. Inform Chin Tradit Med, 2003,20:15-16.
43. Loggia RD, Negra PD, Tubaro A, et al. Homoisoflavanones as anti-inflammatory principles of Muscari comosum [J]. Planta Med, 1989,55:587.
44. Urbancikova M, Masterova I, Toth J. Estrogenic / antiestrogenic activity of homoisoflavonoids from bulbs of Muscari racemosum (L.) Miller [J]. Fitoterapia, 2002,73:724-726.
45. Miadokova E, Masterova I, Vlckova V, et al. Antimutagenic potential of homoisoflavonoids from Muscari racemosum [J]. J Ethnopharmacol, 2002,81:381-386.
46. Yi Y. The cytotoxic constituent of Ophiopogon japonicus [J]. Foreign Med Sci (Chin Tradit Med), 1999,21:42-43.
47. Kamei A, Ichiki H. Antitissue agents and pharmaceutical compositions containing methylophiopogonanone: JP, 2003327529 A2 20031119[P]. 2003-11-19.
48. Choi SY, Yang KM, Jeon SD, et al. Brazilin modulates immune function mainly by augmenting T cell activity in halothane administered mice [J]. Planta Med, 1997,63:405-408.
49. Hu CM, Rang JJ, Lee CC, et al. Induction of vasorelaxation through activation of nitric oxide synthase in endothelial cells by Brazilin [J]. Eur J Pharmacol, 2003,468:37-45.
50. Moon CK, Park KS, Kim SG, et al. Brazilin protects cultured rat hepatocytes from bromochloroform-induced toxicity [J]. Drug Chem Toxicol,1992,15:81-91.
51. Chung JH, Ho JS, Moon CK. Effects of Brazilin on erythrocyte deformability and its related biochemical factors in streptozotocin-induced diabetic rats [J]. Arch Pharm Res, 1988,11:149-154.
52. Tada A, Kanamaru A. Skin-whitening compositions containing 4-n-butylresorcinol and benzopyran derivatives: JP, 2005170910[P]. 2005-06-30.
53. Tada A, Kanamaru A, Saeki Y. Melanocyte dendrite growth Inhibitors containing benzopyranone derivatives and skin preparations containing them: JP, 2004143073 [P]. 2004-05-20.
54. Shim JS, Kim JH, Lee J, et al. Anti-angiogenic activity of a homoisoflavanone from Cremastra appendiculata [J]. Planta Med, 2004,70:171-173.