Phytochemical study of Actaea rubra and biological screenings of isolates

Planta Medica

Volumn 72, Issue 14, 2006, Pages 1350-1352

  Ali, Zulfiqar ^a   Khan, Shabana I ^a   Khan, Ikhlas A ^a,b  

^a UNIVERSITY OF MISSISSIPPI   (United States)

^b UNIVERSITY OF MISSISSIPPI   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

25 O METHYLCIMIGENOL 3 O BETA DEXTRO XYLOPYRANOSIDE; RUBRASIDE A; SITOGLUSIDE; TRITERPENE DERIVATIVE; UNCLASSIFIED DRUG;

ACTAEA; ACTAEA RUBRA; ANIMAL CELL; ANTIOXIDANT ACTIVITY; ARTICLE; COMPLEMENT INHIBITION; CONTROLLED STUDY; CYTOTOXICITY; DRUG ISOLATION; DRUG SCREENING; DRUG STRUCTURE; ESTROGEN ACTIVITY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PHYTOCHEMISTRY; PLANT ROOT; SPECTROSCOPY;

ACTAEA; BIOLOGICAL FACTORS; COMPLEMENT ACTIVATION; HUMANS; MAGNETIC RESONANCE SPECTROSCOPY; PHYTOTHERAPY; PLANT EXTRACTS; PLANT ROOTS; TRITERPENES;

ACTAEA RUBRA;

EID: 33845262060     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-951696     Document Type: Article

References (15)

1. Shao Y, Harris A, Wang M, Zhang H, Cordell G, Bowman M et al. Triterpene glycosides from Cimicifuga racemosa. J Nat Prod 2000; 63: 905-10
2. Wende K, Mugge C, Thurow K, Schopke T, Lindequist U. Actaeaepoxide 3-O-beta-D-xylopyranoside, a new cycloartane glycoside from the rhizomes of Actaea racemosa (Cimicifuga racemosa). J Nat Prod 2001; 64: 986-9
3. Watanabe K, Mimaki Y, Sakagami H, Sashida Y. Cycloartane glycosides from the rhizomes of Cimicifuga racemosa and their cytotoxic activities. Chem Pharm Bull 2002; 50: 121-5
4. Zerega NJC, Mori S, Lindqvist C, Zheng Q, Motley TJ. Using amplified fragment length polemorphisms (AFLPs) to identify black cohosh, (Actaea racemosa). Econ Bot 2002; 56: 154-64
5. Takemoto T, Kusano G, Kawahara M. Studies on the constituents of Cimicifuga spp. VI. Structures of 25-O-acetylcimigenoside and 25-O-methylcimigenoside. Yakugaku Zasshi 1970; 90: 64-7
6. Li CJ, Chen DH, Xiao PG. Chemical constituents of traditional Chinese drug "sheng-ma" (Cimicifuga dahurica). Yaoxue Xuebao 1993; 28: 777-81
7. Kadota S, Li JX, Tanaka K, Namba T. Constituents of Cimicifuga Rhizoma II. Isolation and structures of new cycloartanenol triterpenoids and related compounds from Cimicifuga foetida L. Tetrahedron 1995; 51: 1143-66
8. Kimura O, Sakurai N, Inoue T. Studies on the Chinese crude drug "Shoma." VII. Isolation and determination of genuine natural products, acetyl shengmanol xyloside, 24-O-acetylhydroshengmanol xyloside, and shengmanol xyloside, in Cimicifuga dahurica and the other Cimicifuga plants. Yakugaku Zasshi 1983; 103: 293-9
9. Chen S, Fabricant DS, Santarsiero BD, Mesecar A, Fitzloff JF, Fong HS et al. Isolation, structure elucidation, and absolute configuration of 26-deoxyactein from Cimicifuga racemosa and clarification of nomenclature associated with 27-deoxyactein. J Nat Prod 2002; 65: 601-5
10. Koeda M, Aoki Y, Sakurai N, Nagai M. Studies on the Chinese crude drug "shoma." IX. Three novel cyclolanostanol xylosides, cimicifugosides H-1, H-2 and H-5, from Cimicifuga rhizome. Chem Pharm Bull 1995; 43: 771-6
11. Mustafa J, Khan SI, Ma G, Walker LA, Khan IA. Synthesis, spectroscopic, and biological studies of novel estolides derived from anticancer active 4-O-podophyllotoxinyl 12-hydroxyl-octadec-Z-9-enoate. Lipids 2004; 39: 659-66
12. Tabanca N, Khan SI, Bedir E, Annavarapu S, Willett K, Khan IA et al. Planta Med 2004; 70: 728-35
13. Takamatsu S, Galal AM, Ross SA, Ferreira D, Elsohly MA, Ibrahim AR et al. Antioxidant effect of flavonoids on DCF production in HL-60 cells. Phytother Res 2003; 17: 963-6
14. Lee S, Park J, Lee Y, Lee C, Min B, Kim J et al. Anti-complementary activity of triterpenoides from fruits of Zizyphus jujuba. Biol Pharm Bull 2004; 27: 1883-6
15. Master HE, Khan SI, Poojari KA. Design and synthesis of low molecular weight compounds with complement inhibition activity. Bioorg Med Chem 2005; 13: 4891-9