Chemical constituents from Dysosma versipellis

Chinese Traditional and Herbal Drugs

Volumn 42, Issue 4, 2011, Pages 634-639

  Jiang, Fei ^a   Tian, Hai Yan ^a   Zhang, Jian Long ^a   Ye, Qing Mei ^a   Jiang, Ren Wang ^a,b  

^a JINAN UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

4 ,5 didemethylpodophyllotoxin; Dysosma versipellis (Hance) M. Cheng; Flavonoid; Lignan; Podophyllotoxin; Sterol

Indexed keywords

4' DEMETHYLPODOPHYLLOTOXIN 4 O GLUCOSIDE; 4' NORPODOPHYLLOTOXIN; 4',5' DIDEMETHYLPODOPHYLLOTOXIN; ACETIC ACID ETHYL ESTER; ALCOHOL; BUTANOL; DIPHYLLIN 4 O BETA DEXTRO GLUCOSIDE; DIPROPHYLLINE; DYSOSMA VERSIPELLIS EXTRACT; DYSOSMAROL; FLAVONOID; KAEMPFEROL; KAEMPFEROL 3 O BETA DEXTRO GLUCOSIDE; KAEMPFEROL DERIVATIVE; LIGNAN DERIVATIVE; PICROPODOPHYLLOTOXIN 4 O BETA DEXTRO GLUCOSIDE; PLANT EXTRACT; PODOPHYLLOTOXIN; PODOPHYLLOTOXIN 4 O BETA DEXTRO GLUCOSIDE; PODOPHYLLOTOXIN DERIVATIVE; PODOPHYLLOTOXONE; QUERCETIN; SEPHADEX; SEPHADEX LH 20; SILICA GEL; SITOSTEROL; STEROL; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL COMPOSITION; CHEMICAL STRUCTURE; COLUMN CHROMATOGRAPHY; DRUG DETERMINATION; DRUG ISOLATION; DYSOSMA VERSIPELLIS; FRACTIONATION; MASS SPECTROMETRY; MEDICINAL PLANT; NONHUMAN; PHYSICAL CHEMISTRY; PLANT ROOT; PLANT STEM; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;

EID: 79960318713     PISSN: 02532670     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (18)

1. Ravelli R B G Gigant B, Curmi P A, et al. Insight into tubulin regulation from a complex with colchicines and a stathmin-like domain [J]. Nature, 2004, 428: 198-202. (Pubitemid 38374318)
2. Seiter K. Toxicity of the topoisomerase II inhibitors [J]. Exp Opin Drug Saf, 2005, 4(2): 219-234.
3. Islam M N, Iskander M N. Microtubulin binding sites as target for developing anticancer agents [J]. Mini-Rev Med Chem, 2004, 4(10): 1077-1104. (Pubitemid 39545451)
4. Wang Z Q, Shen Y C, Chen H X, et al. Antitumor agents 126. novel 4β-substituted aniline derivatives of 3′,4′-O,O- didemethylpodophyllotoxin as potent inhibitors of human DNA topoisomerase II [J]. Pharm Res, 1993, 10(3): 343-350.
5. Andrews R C, Teague S J, Meyer A I. Asymmetric total synthesis if (-)-podophylotoxin [J]. J Am Chem Soc, 1988, 110: 7854-7858.
6. Zhao C Q, Huang J, Nagatsu A, et al. Two new podophyllotoxin glucosides from Sinopodophyllum emodi (Wall.) Ying [J]. Chem Pharm Bull, 2001, 49(6): 773-775. (Pubitemid 32587131)
7. Broomhead A J, Dewick P M. Aryltetralin lignans from Linum flavum and Linum capitatum [J]. Phytochemistry, 1990, 29(12): 38-39.
8. Jakka K, Kovuru G, Dodda R, et al. Juspurpurin, an unusual secolignan glycoside from Justicia purpurea [J]. J Nat Prod, 2003, 66(8): 1113-1115.
9. Jiang R W, Zhou J R, Hon P M, et al. Lignans from Dysosma versipellis with inhibitory effects on prostate cancer cell lines [J]. J Nat Prod, 2007, 70(2): 283-286.
10. Markham K P, Ternal B, Stanly R, et al. Carbon 13 NMR studies of flavonoids III. Naturally occurring flavonoid glycosides and their acetylated derivatives [J]. Tetrahedron, 1978, 34: 1389-1389.
11. Shi X, Li X, Liu J, et al. Lignan extraction from the roots of Sinopodophyllum emodi Wall. by matrix solid-phase dispersion [J]. Chromatographia, 2010, 72(7-8): 713-717.
12. Kim Y D, Kim S H, Kim C H, et al. Phylogeny of Berberidaceae based on sequences of the chloroplast gene ndhF [J]. Biochem Syst Ecol, 2004, 32(3): 291-301.