Abstract
A dichloromethane-MeOH extract prepared from the aerial parts of Brickellia veronicaefolia inhibited the spontaneous contractions (IC50 = 39.22 µg/mL) of the guinea-pig ileum. Bioassay-guided fractionation of the extract
led to the isolation of three new benzoic acid derivatives, 1,2-bis-O-(2-methoxybenzoyl)-β-D-glucopyranoside (1), 3-(β-glucopyranosyloxy)benzyl 2,6-dimethoxybenzoate (2) and 3-hydroxybenzyl 2,6-dimethoxybenzoate (3), together with the known compounds taraxasteryl acetate (4), 4-allyl-2-methyloxyphenyl-β-glucopyranoside (5), 2-hydroxy-6-methoxybenzoic acid (6), 2-methoxybenzoic acid (7), chamazulene (8), 2-methoxybenzyl 2-hydroxybenzoate (9), benzyl 2,6-dimethoxybenzoate (10), 3-methoxybenzyl 2-hydroxy-6-methoxybenzoate (11), benzyl 2-hydroxy-6-methoxybenzoate (12), benzyl 2,3,6-trimethoxybenzoate (13), benzyl 2-hydroxy-3,6-dimethoxybenzoate (14) and 3-methoxybenzyl 2,6-dimethoxybenzoate (15). The isolates were characterized by spectral means. Compounds 2 - 6, 8 - 11, 14 and 15 induced a concentration-dependent inhibition of the spontaneous contractions of the
guinea-pig ileum with IC50 values ranging from 1.49 to 4.96 µM. Their activity was comparable to that of papaverine
(IC50 = 4.23 µM).
Key words
Smooth muscle relaxant - benzyl benzoates -
Brickellia veronicaefolia
- Asteraceae - chamazulene
References
- 1 Martínez M. Las plantas medicinales de México. Editorial Botas México, D.F; 1989
- 2
Roberts M F, Timmermann B N, Mabry T J, Brown R, Matlin S A.
Brickellin, a novel flavone from Brickellia veronicaefolia and B. chlorolepsis
.
Phytochemistry.
1984;
23
163-5
- 3
Calderón J S, Quijano L, Cristia M, Gómez F, Ríos T.
Labdane diterpenes from Brickellia veronicaefolia
.
Phytochemistry.
1983;
22
1783-5
- 4
Inhuma M, Roberts M F, Matlin S A, Stacey V E, Timmermann B N, Mabry T J, Brown R.
Synthesis and revised structure of the flavone brickellin.
Phytochemistry.
1985;
24
1367-8
- 5
Roberts M F, Timmermann B N, Mabry T J.
6-Methoxyflavonols from Brickellia veronicaefolia (Compositae).
Phytochemistry.
1980;
19
127-9
- 6
Hernández-Romero Y, Rojas J I, Castillo R, Rojas A, Mata R.
Spasmolytic effects, mode of action and structure-activity relationships of stilbenoids
from Nidema boothii
.
J Nat Prod.
2004;
67
160-7
- 7
Estrada S, Rojas A, Mathison Y, Israel A, Mata R.
Nitric oxide/cGMP mediates the spasmolytic action of 3,4′-dihydroxy-5,5′-dimethoxybibenzyl
from Scaphyglottis livida
.
Planta Medica.
1999;
65
109-14
- 8
Rojas A, Cruz S, Rauch V, Bye R, Linares E, Mata R.
Spasmolytic potential of some plants used in Mexican traditional medicine for the
treatment of gastrointestinal disorders.
Phytomedicine.
1995;
2
51-5
- 9 Bailey N TJ. Statistical methods in biology. Cambridge; Cambridge University Press
1995: 234-36
- 10
Reynolds W F, Sawyer J F, Enríquez R G, Escobar L I, Chávez M A, Shoolery J N.
Total assignment of the 13C spectrum of taraxasteryl acetate by 13C-13C connectivity experiments and determination of the stereochemistry of taraxasterol
by X-ray diffraction.
Can J Chem.
1985;
63
1048-54
- 11
Schwab W, Scheller G, Schreier P.
Glycosidically bound aroma components from sour cherry.
Phytochemistry.
1990;
29
607-12
- 12
Bohlmann F, Chen Z L, Schuster A.
Aromatic esters from Solidago decurrens
.
Phytochemistry.
1981;
20
2601-2
- 13
Bertelli D J, Crabtree J H.
Naturally occurring fulvene hydrocarbons.
Tetrahedron.
1968;
24
2079-89
- 14
Kodpinid M, Sadavongvivad C, Thebtaranonth C, Thebtaranonth Y.
Benzyl benzoates from the root of Uvaria purpurea
.
Phytochemistry.
1984;
23
199-200
- 15
Bohlmann F, Jakupovic J, Lonitz M.
Naturally occurring terpenes derivatives, 76. Constituents of the Eupatorium group.
Chem Ber.
1977;
110
301-14
- 16
Yueh-Hsiung K, Ping-Hung L, Yung-Shun W.
Four new compounds from the seeds of Cassia fistula
.
J Nat Prod.
2002;
65
1165-7
- 17
Inouye H, Nakamura Y.
Die Struktur der beiden stark bitter schmeckenden Glucoside Amarogentin und Amaroswerin
aus Swertia japonica
.
Tetrahedron.
1971;
27
1951-66
- 18
Kirimer N, Tunalier Z, Basser K H, Cingi I.
Antispasmodic and spasmogenic of Scolymus hispanicus and taraxasteryl acetate on isolated ileum preparations.
Planta Medica.
1997;
63
556-8
- 19
Rekka E, Chrysselis M, Siskou I, Kourounakis A.
Synthesis of new azulene derivatives and study of their effect on lipid peroxidation
and lipoxygenase activity.
Chem Pharm Bull.
2002;
50
904-7
- 20
Heneka N.
Chamomilla recutita
.
Aust J Med Herbalism.
1993;
5
33-9
- 21
Safahyi H, Sabieraj J, Sailer E -R, Ammon H.
Chamazulene: an antioxidant-type inhibitor of leukotriene B4 formation.
Planta Medica.
1994;
60
410-3
Dr. Rachel Mata
Facultad de Química
Universidad Nacional Autónoma de México
Coyoacán 04510
México City
México
Phone: +525-55-622 5289
Fax: +525-55-622 5329
Email: rachel@servidor.unam.mx