2012
DOI: 10.1021/np300395m
|View full text |Cite
|
Sign up to set email alerts
|

Antiviral Chromones from the Stem of Cassia siamea

Abstract: Seven new chromones, siamchromones A-G (1-7), and 12 known chromones (8-19) were isolated from the stems of Cassia siamea. Compounds 1-19 were evaluated for their antitobacco mosaic virus (anti-TMV) and anti-HIV-1 activities. Compound 6 showed antitobacco mosaic virus (anti-TMV) activity with an inhibition rate of 35.3% and IC50 value of 31.2 μM, which is higher than that of the positive control, ningnamycin. Compounds 1, 10, 13, and 16 showed anti-TMV activities with inhibition rates above 10%. Compounds 4, 6… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2

Citation Types

0
35
0

Year Published

2013
2013
2020
2020

Publication Types

Select...
7
1

Relationship

2
6

Authors

Journals

citations
Cited by 85 publications
(36 citation statements)
references
References 26 publications
(38 reference statements)
0
35
0
Order By: Relevance
“…The 1 H and 13 C NMR spectra of 2 were similar to those of 1 at C-1ZC-6, C-1 0 ZC-6 0 and C-1 00 ZC-6 00 . The major difference resulted from the replacement of the prenyl group in 1 by a 2-oxopropyl group, -CH 2 C(O)CH 3 (Hu et al 2012) [d C 48.6 t, 206.8 s and 28.9 q; d H 4.30 (2H, s) and 2.31 (3H, s)] in 2. The HMBC correlations of H-7 00 (d H 4.30) with C-4 00 (d C 144.7), C-5 00 (d C 128.3) and C-6 00 (d C 124.8), and of H-6 00 (d H 6.92) with C-7 00 (d C 48.6) indicated that the 2-oxopropyl group was attached to C-5 00 .…”
Section: Resultsmentioning
confidence: 99%
“…The 1 H and 13 C NMR spectra of 2 were similar to those of 1 at C-1ZC-6, C-1 0 ZC-6 0 and C-1 00 ZC-6 00 . The major difference resulted from the replacement of the prenyl group in 1 by a 2-oxopropyl group, -CH 2 C(O)CH 3 (Hu et al 2012) [d C 48.6 t, 206.8 s and 28.9 q; d H 4.30 (2H, s) and 2.31 (3H, s)] in 2. The HMBC correlations of H-7 00 (d H 4.30) with C-4 00 (d C 144.7), C-5 00 (d C 128.3) and C-6 00 (d C 124.8), and of H-6 00 (d H 6.92) with C-7 00 (d C 48.6) indicated that the 2-oxopropyl group was attached to C-5 00 .…”
Section: Resultsmentioning
confidence: 99%
“…Since certain flavonoids exhibit potential anti‐TMV activity, compounds 1–8 were tested for their anti‐TMV activity. The anti‐TMV activity was tested using the half‐leaf method . Ningnanmycin (a commercial product for plant disease in China) was used as a positive control.…”
Section: Resultsmentioning
confidence: 99%
“…The long-range correlation of the methoxy proton signal (δ H 3.81) with C-2 (δ C 155.4) clearly indicated that the methoxy group located at C-2. The HMBC correlations of H-1' (δ H 3.58) Since certain of the phenolic compounds exhibit potential anti-TMV activity [19][20][21] , compounds 1 was tested for it anti-tobacco mosaic virus activity. The anti-TMV activities were tested using the half-leaf method 21 .…”
Section: Asian Journal Of Chemistry Asian Journal Of Chemistrymentioning
confidence: 99%
“…The HMBC correlations of H-1' (δ H 3.58) Since certain of the phenolic compounds exhibit potential anti-TMV activity [19][20][21] , compounds 1 was tested for it anti-tobacco mosaic virus activity. The anti-TMV activities were tested using the half-leaf method 21 . Ningnanmycin (2 % water solution), a commercial product for plant disease in China, was used as a positive control.…”
Section: Asian Journal Of Chemistry Asian Journal Of Chemistrymentioning
confidence: 99%