SMB00246
Calceolarioside A
≥95% (LC/MS-ELSD)
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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
MDL编号:
UNSPSC代码:
12352205
PubChem化学物质编号:
NACRES:
NA.25
方案
≥95% (LC/MS-ELSD)
表单
solid
应用
metabolomics
vitamins, nutraceuticals, and natural products
储存温度
−20°C
SMILES字符串
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
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
InChI key
UHIGZYLCYRQESL-VJWFJHQPSA-N
一般描述
Natural product derived from plant source.
应用
Calceolarioside A has been used in flow cytometric analysis.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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
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
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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