Abstract
Sarcolobus globosus is a medicinal plant growing in mangrove forests in Asia. No constituents from this
plant have been reported previously. From the diethyl ether extract of S. globosus a new rotenoid sarcolobin and a new isoflavone sarcolobone, as well as the previously
known rotenoids tephrosin, 12aα-hydroxydeguelin, 11-hydroxytephrosin, 12a-hydroxyrotenone,
12aα-hydroxyrotenone, 6aα,12aα-12a-hydroxyelliptone, 6a,12a-dehydrodeguelin, 13-homo-13-oxa-6a,12a-dehydrodeguelin, the isoflavone barbigerone and a chromone 6,7-dimethoxy-2,3-dihydrochromone
were identified. 6,7-Dimethoxy-2,3-dihydrochromone has not previously been reported
as a natural product.
Key words
Sarcolobus globosus
- Asclepiadaceae - rotenoid - isoflavonoid - mangrove forest
References
- 1 Johnson T. CRC ethnobotany desk reference. Boca Raton, FL; CRC Press 1999
- 2
Arokiasamy M.
Toxicity of Sarcolobus globosus as observed in a cat.
Malaysian Vet J.
1968;
4
196-9
- 3
Mustafa M R.
Inhibition of calcium dependent contractions of the isolated guinea pig ileal longitudinal
muscle and taenia coli by the total glycosidic extract of the plant Sarcolobus globosus
.
Toxicon.
1993;
31
67-74
- 4 Dewick P M. Isoflavonoids.
In: The flavonoids: Advances in research since 1986,. JB Harborne, editor London; Chapman & Hall 1993: pp 117-238
- 5
Wangensteen H, Samuelsen A B, Malterud K E.
Antioxidant activity in extracts from coriander.
Food Chem.
2004;
88
293-7
- 6
Pereira A S, Pinto A C, Cardoso J N, Neto F RA, Vieira P C, Fernandes J B. et al
.
Analysis of rotenoids by high temperature high resolution gas chromatography-mass
spectrometry.
J High Resol Chromatogr.
1998;
21
513-8
- 7
Luyengi L, Lee I S, Mar W, Fong H HS, Pezzuto J M, Kinghorn A D.
Rotenoids and chalcones from Mundulea sericea that inhibit phorbol ester-induced ornithine decarboxylase activity.
Phytochemistry.
1994;
36
1523-6
- 8
Patil A D, Freyer A J, Eggleston D S, Haltiwanger R C, Bean M F, Taylor P B. et al
.
The inophyllums, novel inhibitors of HIV-1 reverse transcriptase isolated from the
Malaysian tree, Calophyllum inophyllum L.
J Med Chem.
1993;
36
4131-8
- 9
Unai T, Yamamoto I, Cheng H M, Casida J E.
Synthesis and stereochemical characterization of hydroxy- and epoxy-derivatives of
rotenone.
Agric Biol Chem.
1973;
37
387-401
- 10
Tahara S, Narita E, Ingham J L, Mizutani J.
New rotenoids from the root bark of Jamaican dogwood (Piscidia erythrina L.)
Z Naturforsch Teil C.
1990;
45
154-60
- 11
Ito C, Itoigawa M, Kojima N, Tan H TW, Takayasu J, Tokuda H. et al .
Cancer chemopreventive activity of rotenoids from Derris trifoliata
.
Planta Med.
2004;
70
585-8
- 12 Agrawal P K. Carbon-13 NMR of flavonoids. Amsterdam; Elsevier 1989
- 13
Kaouadji M, Agban A, Mariotte A M.
Lonchocarpene, a stilbene, and lonchocarpusone, an isoflavone: Two new pyranopolyphenols
from Lonchocarpus nicou roots.
J Nat Prod.
1986;
49
281-5
- 14
Dagne E, Bekele A.
C-Prenylated isoflavones from Millettia ferruginea
.
Phytochemistry.
1990;
29
2679-82
- 15
Blatt C TT, Chávez D, Chai H Y, Graham J G, Cabieses F, Farnsworth N R. et al .
Cytotoxic flavonoids from the stem bark of Lonchocarpus aff. fluvialis
.
Phytother Res.
2002;
16
320-5
- 16
Fang N B, Casida J E.
Cubé resin insecticide: Identification and biological activity of 29 rotenoid constituents.
J Agric Food Chem.
1999;
47
2130-6
- 17
Andrei C C, Viera P C, Fernandes J B, Silva M FGF, Fo E R.
Dimethylchromene rotenoids from Tephrosia candida
.
Phytochemistry.
1997;
46
1081-5
- 18
Van Puyvelde L, De Kimpe N, Mudaheranwa J P, Gasiga A, Schamp N, Declercq J P. et
al .
Isolation and structural elucidation of potentially insecticidal and acaricidal isoflavone-type
compounds from Neorautanenia mitis.
.
J Nat Prod.
1987;
50
349-56
Helle Wangensteen
Department of Pharmacognosy
School of Pharmacy
University of Oslo
P. O. Box 1068 Blindern
0316 Oslo
Norway
Telefon: +47-22-85-65-49
Fax: +47-22-85-75-05
eMail: helle.wangensteen@farmasi.uio.no