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Merck

SMB00204

Sigma-Aldrich

Nirtetralin

≥95% (LC/MS-ELSD)

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CHF 391.00

CHF 391.00


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1 MG
CHF 391.00

About This Item

Empirische Formel (Hill-System):
C24H30O7
CAS-Nummer:
Molekulargewicht:
430.49
UNSPSC-Code:
12352205
PubChem Substanz-ID:
NACRES:
NA.25

CHF 391.00


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Assay

≥95% (LC/MS-ELSD)

Form

solid

Anwendung(en)

metabolomics
vitamins, nutraceuticals, and natural products

Lagertemp.

−20°C

SMILES String

COC[C@H]1Cc2cc3OCOc3c(OC)c2[C@H]([C@@H]1COC)c4ccc(OC)c(OC)c4

InChI

1S/C24H30O7/c1-25-11-16-8-15-10-20-23(31-13-30-20)24(29-5)22(15)21(17(16)12-26-2)14-6-7-18(27-3)19(9-14)28-4/h6-7,9-10,16-17,21H,8,11-13H2,1-5H3/t16-,17-,21+/m1/s1

InChIKey

LHQDZANQXMRHIV-LZJOCLMNSA-N

Allgemeine Beschreibung

Natural product derived from plant source.

Biochem./physiol. Wirkung

Nirtetralin, along with nirtetralin A and B, have shown to suppress the secretion of the HBV antigens in a dose-dependent manner when assayed for anti-hepatitis B virus activities in vitro.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Die Dokumentenbibliothek aufrufen

Ray-Ling Huang et al.
Phytotherapy research : PTR, 17(5), 449-453 (2003-05-16)
Using an HBV-producing cell line and inhibition of the expression of the HBsAg and HBeAg as antiviral indicators, a study was conducted on 25 compounds isolated from four Phyllanthus (Euphorbiaceae) plants, including P. amarus Schum. & Thonn., P. multi florus
Cândida A L Kassuya et al.
European journal of pharmacology, 546(1-3), 182-188 (2006-08-24)
Previous studies have shown that the extracts obtained from Phyllanthus amarus, and some of the lignans isolated from it, exhibit pronounced antiinflammatory properties. In the present study, we have assessed whether the antiinflammatory actions of these lignans can be mediated
Wanxing Wei et al.
Phytotherapy research : PTR, 26(7), 964-968 (2011-12-02)
One new lignan, nirtetralin B, along with its two known stereoisomers were isolated from Phyllanthus niruri L. The structure of the new compound was determined by spectroscopy experiments and x-ray diffraction analysis. These lignans were assayed for anti-hepatitis B virus
Minh Giang Phan et al.
Chemical & pharmaceutical bulletin, 54(4), 546-549 (2006-04-06)
From the aerial parts of Scoparia dulcis L. (Scrophulariaceae) grown in Vietnam, four scopadulane-type diterpenoids (4-7), of which 7 is new and was given the trivial name scopadulcic acid C, together with nine known compounds were isolated. Their structures were

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