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Merck

SMB00204

Sigma-Aldrich

Nirtetralin

≥95% (LC/MS-ELSD)

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About This Item

Fórmula empírica (notación de Hill):
C24H30O7
Número de CAS:
Peso molecular:
430.49
UNSPSC Code:
12352205
PubChem Substance ID:
NACRES:
NA.25

assay

≥95% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−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

InChI key

LHQDZANQXMRHIV-LZJOCLMNSA-N

General description

Natural product derived from plant source.

Biochem/physiol Actions

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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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
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
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

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