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SMB00246

Sigma-Aldrich

Calceolarioside A

≥95% (LC/MS-ELSD)

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About This Item

Formula empirica (notazione di Hill):
C23H26O11
Numero CAS:
84744-28-5
Peso molecolare:
478.45
Numero MDL:
MFCD24849378
Codice UNSPSC:
12352205
ID PubChem:
329824899
NACRES:
NA.25

Saggio

≥95% (LC/MS-ELSD)

Forma fisica

solid

applicazioni

metabolomics
vitamins, nutraceuticals, and natural products

Temperatura di conservazione

−20°C

Stringa SMILE

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
UHIGZYLCYRQESL-VJWFJHQPSA-N

Categorie correlate

Descrizione generale

Natural product derived from plant source.

Applicazioni

Calceolarioside A has been used in flow cytometric analysis.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

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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
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
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
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
Targeting Malassezia species for novel synthetic and natural antidandruff agents.
Letizia A, et al.
Current Medicinal Chemistry, 24(22), 2392-2412 (2017)
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