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SMB00246

Calceolarioside A

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About This Item

Empirical Formula (Hill Notation):
C23H26O11
CAS Number:
Molecular Weight:
478.45
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352205
MDL number:
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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.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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
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
Targeting Malassezia species for novel synthetic and natural antidandruff agents.
Letizia A, et al.
Current Medicinal Chemistry, 24(22), 2392-2412 (2017)
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
Do-Sung Kim et al.
European journal of pharmacology, 541(1-2), 24-32 (2006-06-20)
Adriamycin is a potent antitumor drug that is known to cause severe cardiotoxicity. This study examined the protective effect of calceolarioside on adriamycin-induced cardiomyocyte toxicity. Calceolarioside significantly inhibited the adriamycin induced cell death and caspase-3 activation, which may be explained

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