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SMB00204

Sigma-Aldrich

Nirtetralin

≥95% (LC/MS-ELSD)

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About This Item

Empirical Formula (Hill Notation):
C24H30O7
CAS Number:
50656-78-5
Molecular Weight:
430.49
UNSPSC Code:
12352205
PubChem Substance ID:
329824866
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

Related Categories

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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