2003
DOI: 10.1590/s0102-695x2003000200005
|View full text |Cite
|
Sign up to set email alerts
|

Substâncias isoladas das folhas de Bauhinia microstachya (Raddi) Macbr. (Caesalpiniaceae)

Abstract: RESUMO:Neste trabalho é relatado o isolamento de três substâncias das folhas de Bauhinia microstachya (Raddi) Macbr., Caesalpiniaceae, incluindo dois constituintes isolados pela primeira vez nesta espécie, a vitexina e o hidrocarboneto hexatriacontano. As estruturas desses compostos foram estabelecidas através de estudos de RMN- INTRODUÇÃOEntre as inúmeras espécies vegetais de interesse medicinal estão as plantas do gênero Bauhinia, pertencentes à família Caesalpiniaceae, as quais podem ser encontradas, princ… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
4
0

Year Published

2009
2009
2020
2020

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 8 publications
(6 citation statements)
references
References 11 publications
1
4
0
Order By: Relevance
“…The doublet centered at δ H 5.97 with J = 9:55 Hz, typical for trans-diaxial coupling, was attributed to H-1" from anomeric carbon. The signals observed between δ H 3.00 and 5.00 combined with data from the literature suggest the structure of a glucose moiety (Bianco & Santos 2003). The positioning of the sugar at C-8 was confirmed by heteronuclear multiple bond correlation (HMBC) through the correlations between H-1" and the signal at δ C 157.5 (C-9) and between H-6 and the carbons of ring A, especially the correlation with the signals at δ C 164.8 (C-7), δ C 165.1 (C-5), δ C 105.4 (C-10).…”
Section: Resultssupporting
confidence: 52%
“…The doublet centered at δ H 5.97 with J = 9:55 Hz, typical for trans-diaxial coupling, was attributed to H-1" from anomeric carbon. The signals observed between δ H 3.00 and 5.00 combined with data from the literature suggest the structure of a glucose moiety (Bianco & Santos 2003). The positioning of the sugar at C-8 was confirmed by heteronuclear multiple bond correlation (HMBC) through the correlations between H-1" and the signal at δ C 157.5 (C-9) and between H-6 and the carbons of ring A, especially the correlation with the signals at δ C 164.8 (C-7), δ C 165.1 (C-5), δ C 105.4 (C-10).…”
Section: Resultssupporting
confidence: 52%
“…The vitexin spectrum shows absorption bands corresponding to the functional groups –OH, C=C (aromatic), H–C (aromatic) and O–C (aromatic), respectively 3200-3650 cm −1 , 1450-1600 cm −1 , 3050 -3150 cm −1 and 1000-1300 cm −1 , as described by [ 40 ]. The absorption of conjugated carbonyl and intramolecular hydrogen bonding occurs approximately at 1665 cm −1 and medium-sized signals between 1600 and 1500 cm −1 also indicate the presence of aromatic groups in this molecule [ 41 ].…”
Section: Resultsmentioning
confidence: 99%
“…Reddy et al (2003) More recently, Rao et al (2008), searching for new antiinflammatory natural agents, isolated six known flavonoids from the aerial parts of B. variegata, namely kaempferol, ombuin, kaempferol 7,4′-dimethyl ether 3-O-β-Dglucopyranoside, kaempferol 3-O-β-D-glucopyranoside, isorhamnetin 3-O-β-D-glucopyranoside and hesperidin, together with one triterpene caffeate, 3-β-trans-(3,4dihydroxycinnamoyloxy) olean-12-en-28 oic acid. Another species, B. microstachya, showed the presence of phenolic metabolites (da Silva and Cechinel Filho, 2002) as well as vitexin, methyl gallate and hexatriacontane (Bianco and Santos, 2003). Pettit et al (2006) Almeida et al, 2004).…”
Section: Phytochemical Knowledge Of the Genus Bauhiniamentioning
confidence: 99%