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About This Item
经验公式（希尔记法）:
C23H26O11
CAS号:
分子量:
478.45
MDL號碼:
分類程式碼代碼:
12352205
PubChem物質ID:
NACRES:
NA.25
推荐产品
化驗
≥95% (LC/MS-ELSD)
形狀
solid
應用
metabolomics
vitamins, nutraceuticals, and natural products
儲存溫度
−20°C
SMILES 字串
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 密鑰
UHIGZYLCYRQESL-VJWFJHQPSA-N
一般說明
Natural product derived from plant source.
應用
Calceolarioside A has been used in flow cytometric analysis.
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
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
Targeting Malassezia species for novel synthetic and natural antidandruff agents.
Letizia A, et al.
Current Medicinal Chemistry, 24(22), 2392-2412 (2017)
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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