Chemical constituents of Excoecaria acerifclia

Zhongguo Zhongyao Zazhi

Volumn 36, Issue 14, 2011, Pages 1969-1974

  Hu, Jiang ^a,b   Zhang, Lanchun ^c   Zhao, Qinshi ^a  

^a KUNMING INSTITUTE OF BOTANY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c KUNMING MEDICAL UNIVERSITY   (China)

Author keywords

Chemical constituents; Excoecaria acerifclia; Triterpenoids, phenylpropanoids

Indexed keywords

11 HYDROXY 3 OXO 12 URSEN 28 OIC ACID; 2ALPHA,3BETA,24 TRIHYDROXY 12 URSEN 28 OIC ACID; 6 HYDROXY 20(29) LUPEN 3 ONE; 7,8 TRANS 4,5,9,9' TETRAHYDROXY 3,3',9 DIMETHOXY 7 O 5', 8 O 4' NEOLIGNAN; APELIN; APIGENIN; CATECHIN; ISOLUPENYL ACETATE; KAEMPFEROL; KAMEPFEROL 3 O BETA DEXTRO GALACTOPYRANOSIDE; MALLOAPELIN C; NEOLIGNAN; PYRANOSIDE; QUERCETIN; SEPHADEX; SILICA GEL; SYRINGARESINOL; TRITERPENOID; UNCLASSIFIED DRUG;

ARTICLE; COLUMN CHROMATOGRAPHY; EXCOECARIA ACERIFCLIA; MEDICINAL PLANT; NONHUMAN; PURIFICATION;

CHROMATOGRAPHY; DRUGS, CHINESE HERBAL; EUPHORBIACEAE; ORGANIC CHEMICALS;

EID: 80053398546     PISSN: 10015302     EISSN: None     Source Type: Journal    
DOI: 10.4268/cjcmm20111427     Document Type: Article

References (15)

1. Kim T H, Ito H, Hayashi K, et al. Aromatic constituents from the Heartwood of Santalum album L[J]. Chem Pharm Bull, 2005, 53(6):641.
2. Son Y K, Lee M H, Han Y N, et al. A new antipsychotic effective neolignan from Firmiana simplex[J]. Arch Pharm Res, 2005, 28(1):34.
3. Xu J Fu, Feng Z M, Liu J, et al. New hepatoprotective coumarino-lignoids from Mallotus apelta[J]. Chem Biodivers, 2008, 5(4):591.
4. Abea F, Yamauchi T. 9α-Hydroxypinoresinol,9α- hydroxymedioresinol and related lignans from Allamanda neriifolia[J]. Phytochemistry, 1988, 27:575.
5. Wang B H, Polya G M. Selective inhibition of cyclic AMP-dependent protein kinase by amphiphilic triterpenoids and related compounds[J]. Phytochemistry, 1996, 41:55.
6. Santos G G, Alves J C N, Rodilla J M L, et al. Terpenoids and other constituents of Eucalyptus globulus[J]. Phytochemistry, 1997, 44:1309.
7. 13C-NMR chemical shifts of some lupanols from Pleurostylia opposita[J]. Phytochemistry, 1982, 21:2065.
8. 13C Nuclear magnetic resonance of lupane-type triterpenes, lupeol, betulin and betulinic acid[J]. Chem Pharm Bull, 1980, 28(3):1006.
9. El-Sayed N H, Wojcińska M, Drost-Karbowska T, et al. Kaempferol triosides from Silphium perfoliatum[J]. Phytochemistry, 2002, 60:835.
10. Kingston D G I, Fales H M, Methane chemical ionization mass spectrometry of flavonoids[J]. Tetrahedron, 1973, 29:4083.
11. Berghöfer R, Hölzl J. Biflavonoids in hypericum perforatum; Part 1. Isolation of I3, II8-biapigenin[J]. Planta Med, 1987, 53:216.
12. Tsiklauri G C, Proanthocyanidins from Laurocerasus officinalis leaves[J]. Khimiya Prirodnykh Soedinenii, 1978, 4:526.
13. Ishimaru K, Nonaka G, Nishioka I, Flavan-3-ol and procyanidin glycosides from Quercus miyagii[J]. Phytochemistry, 1987, 26:1167.
14. Tuckmantel W, Kozikowski A P, Romanczyk L J. Methods for their preparation of catechin and epicatechin dimmers: CN 1354743[P]. 2002-06-19