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Merck

SMB00094

Sigma-Aldrich

Catalposide

≥95% (LC/MS-ELSD)

Synonym(e):

Hydroxybenzoyl catalpol

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About This Item

Empirische Formel (Hill-System):
C22H26O12
CAS-Nummer:
Molekulargewicht:
482.43
EG-Nummer:
UNSPSC-Code:
12352205
PubChem Substanz-ID:
NACRES:
NA.25

Assay

≥95% (LC/MS-ELSD)

Form

solid

Anwendung(en)

metabolomics
vitamins, nutraceuticals, and natural products

Lagertemp.

−20°C

SMILES String

CC.OC[C@H]1O[C@@H](O[C@@H]2OC=C[C@H]3[C@H](OC(=O)c4ccc(O)cc4)[C@@H]5O[C@]5(CO)[C@@H]23)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C22H26O12.C2H6/c23-7-12-14(26)15(27)16(28)21(31-12)33-20-13-11(5-6-30-20)17(18-22(13,8-24)34-18)32-19(29)9-1-3-10(25)4-2-9;1-2/h1-6,11-18,20-21,23-28H,7-8H2;1-2H3/t11-,12-,13-,14-,15+,16-,17+,18+,20+,21+,22-;/m1./s1

InChIKey

HDJSRSCFWHTJOZ-BNQCZGKOSA-N

Allgemeine Beschreibung

Natural product derived from plant source.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Die Dokumentenbibliothek aufrufen

Ji Hae Lee et al.
Biochemical and biophysical research communications, 422(4), 568-572 (2012-05-16)
Peroxisome proliferator-activated receptor-alpha (PPARα) is a nuclear receptor that regulates the expression of genes related to cellular lipid uptake and oxidation. Thus, PPARα agonists may be important in the treatment of hypertriglyceridemia and hepatic steatosis. In this study, we demonstrated
Eun Jeong Park et al.
Biomedical chromatography : BMC, 23(9), 980-986 (2009-04-09)
Verproside, isovanilloylcatalpol, catalposide and 6-O-veratroyl catalpol are bioactive iridoid glucosides isolated from in a number of folk medicinal plants. A rapid, sensitive and selective liquid chromatography/mass spectrometric (LC/MS) method for the simultaneous determination of verproside, isovanilloylcatalpol, catalposide and 6-O-veratroyl catalpol
Hyuncheol Oh et al.
Planta medica, 68(8), 685-689 (2002-09-11)
Catalposide (1) and two related iridoids were isolated from the stem of Catalpa ovata (Bignoniaceae) by bioassay guided fractionation. Catalposide (1) significantly inhibited the production of nitric oxide (NO) in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages in a dose-dependent manner. RT-PCR
Mi Kyoung Moon et al.
Toxicology letters, 145(1), 46-54 (2003-09-10)
Catalposide, the major iridoid glycoside isolated from the stem bark of Catalpa ovata G. Don (Bignoniaceae) has been shown to possess anti-microbial, anti-tumoral, and anti-inflammatory properties. Heme oxygenase-1 (HO-1) is a stress response protein and is known to play a
S J An et al.
International immunopharmacology, 2(8), 1173-1181 (2002-09-28)
Catalposide, the major iridoid glycoside isolated from the stem bark of Catalpa ovata G. Don (Bignoniaceae), was found to inhibit the productions of tumor necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta), and interleukin-6 (IL-6), and the activation of nuclear factor kappaB (NF-kappaB)

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