Found 1 publication.
Displayed publication 1
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (Article ID: 11313)
de Almeida AP, Miranda MMFS, Simoni IC, Wigg MD, Lagrota MHC, Costa SS
Flavonol monoglycosides isolated from the antiviral fractions of Persea americana (Lauraceae) leaf infusion
Phytotherapy Research 12(8) (1998)
562-567
An infusion of Persea americana leaves (Lauraceae) strongly inhibited herpes simplex virus type 1 (HSV-1), Aujeszky's disease virus (ADV) and adeno virus type 3 (AD3) in cell cultures. Its fractionation, guided by anti-HSV-1 and ADV assays, allowed the isolation and identification of two new flavonol monoglycosides, kaempferol and quercetin 3-O-alpha-D-arabinopyranosides, along with the known kaempferol 3-O-alpha-L-rhamnopyranoside (afzelin), quercetin 3-O-alpha-L-rhamnopyranoside (quercitrin), quercetin 3-O-beta-glucopyranoside and quercetin, The known quercetin 3-O-beta-galactopyranoside was identified in a mixture. Afzelin and quercetin 3-O-alpha-D-arabinopyranoside showed higher activity against acyclovir-resistant HSV-I, Chlorogenic add significantly inhibited the HSV-1 replication without any cytotoxicity. However, all the substances tested were less active than the infusion or fractions. The same substances did not affect ADV replication. Chemical structures were elucidated by the analysis of UV, H-1 and C-13 NMR data, mainly by APT, homo and heteronuclear COSY experiments. The configuration of the D-arabinose unit, not usual in natural plant products, was established on the basis of the optical rotation of the free sugar obtained after acid hydrolysis.
quercetin, leaves, quercitrin, Persea americana, kaempferol 3-o-alpha-d-arabinopyranoside, quercetin 3-o-alpha-d-arabinopyranoside, afzelin, quercetin 3-o-beta-glucopyranoside, quercetin 3-o-beta-galactopyranoside, chlorogenic acid, herpes simplex virus type 1, aujeszky's disease virus, adenovirus type 3
Publication DOI: 10.1002/(SICI)1099-1573(199812)12:8<562::AID-PTR356>3.0.CO;2-6Journal NLM ID: 8904486Publisher: Chichester: Wiley
Institutions: Núcleo de Pesquisas de Produtos Naturais, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil, Instituto de Microbiologia, Departamento de Virologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil, Instituto Biológico de São Paulo, Seção de Biologia Celular, São Paulo, Brazil
Methods: 13C NMR, 1H NMR, TLC, acid hydrolysis, paper chromatography, UV, optical rotation measurement, CC, melting point determination, antiviral assay
The publication contains the following compound(s):
- Compound ID: 21438
Structure type: monomer
Trivial name: isoquercitrin
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
Reference(s) to other database(s): CCSD:
49965, CBank-STR:953
- Compound ID: 22453
Structure type: monomer
C21H20O11
Trivial name: quercitrin, baohuoside-II, quercetin 3-rhamnoside, quercetin 3-O-rhamnoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
49971, CBank-STR:599
- Compound ID: 26724
Structure type: monomer
Trivial name: afzelin
Compound class: glycoside, flavonoid glycoside, triterpenoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
41324, CBank-STR:605
- Compound ID: 28577
Structure type: monomer
Compound class: glycoside
- Compound ID: 28578
Structure type: monomer
Compound class: glycoside
- Compound ID: 28579
Structure type: monomer
Compound class: glycoside
Expand this publication
Collapse this publication
Total list of publication IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
Execution: <1 sec