SMB00246
Calceolarioside A
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关于此项目
经验公式（希尔记法）:
C23H26O11
化学文摘社编号:
分子量:
478.45
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352205
MDL number:
InChI
1S/C23H26O11/c24-11-18-22(34-19(29)6-3-12-1-4-14(25)16(27)9-12)20(30)21(31)23(33-18)32-8-7-13-2-5-15(26)17(28)10-13/h1-6,9-10,18,20-28,30-31H,7-8,11H2/b6-3+/t18-,20-,21-,22-,23-/m1/s1
SMILES string
OC[C@H]1O[C@@H](OCCc2ccc(O)c(O)c2)[C@H](O)[C@@H](O)[C@@H]1OC(=O)\C=C\c3ccc(O)c(O)c3
InChI key
UHIGZYLCYRQESL-VJWFJHQPSA-N
form
solid
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
General description
Natural product derived from plant source.
Application
Calceolarioside A has been used in flow cytometric analysis.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Avijit Poddar et al.
Planta medica, 74(5), 503-508 (2008-06-11)
Bioactivity-guided fractionation has led to the successful isolation of calceolarioside A ( 1) from the methanolic extract of night jasmine leaves. The in vitro antileishmanial activity of compound 1 was determined (IC (50) = 20 microg/mL). Its IN VIVO efficacy
José G Sena Filho et al.
Journal of natural products, 72(7), 1344-1347 (2009-06-03)
Many references to the use of Lantana spp. can be found in the ethnopharmacological literature from locations around the globe. This study was focused on examining constituents from the polar extracts of Lantana radula Sw. and Lantana canescens Kunth, for
A Capasso et al.
Planta medica, 59(4), 337-339 (1993-08-01)
The effect of calceolarioside A, a phenylpropanoid glycoside (PhG), isolated from Calceolaria hypericina, was studied on rabbit platelets in vitro. Calceolarioside A induced a dose-related aggregant effect on rabbit platelets. Indomethacin did not modify the calceolarioside A-induced aggregant effect. Furthermore
Targeting Malassezia species for novel synthetic and natural antidandruff agents.
Letizia A, et al.
Current Medicinal Chemistry, 24(22), 2392-2412 (2017)
S Damtoft et al.
Phytochemistry, 37(2), 441-443 (1994-09-01)
From Chirita sinensis (Gesneriaceae) was isolated six phenylethanoid glucosides, namely the previously known positional isomers plantainoside A, calceolarioside A and calceolarioside B together with three new compounds named chiritoside A, B and C. It was proved by analysis of the
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