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SML2337

Sigma-Aldrich

Diasarone-I

≥98% (HPLC)

Synonym(s):

(E)-3-ethyl-2-methyl-3-(2′′,4′′,5′′-trimethoxy)phenyl-1-(2′,4′,5′-trimethoxy)phenyl-1-propene, 1,1′-[(1E)-3-Ethyl-2-methyl-1-propene-1,3-diyl]bis[2,4,5-trimethoxybenzene], Diasarone 1, Diasarone I, NEOLASA-I

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5 MG
$67.54
25 MG
$287.00

About This Item

Empirical Formula (Hill Notation):
C24H32O6
CAS Number:
Molecular Weight:
416.51
UNSPSC Code:
12352200
NACRES:
NA.77

$67.54

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Available to ship onMay 05, 2025Details


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assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

−20°C

SMILES string

C/C(C(CC)C1=CC(OC)=C(OC)C=C1OC)=C\C2=C(OC)C=C(OC)C(OC)=C2

InChI

1S/C24H32O6/c1-9-17(18-12-22(28-6)24(30-8)14-20(18)26-4)15(2)10-16-11-21(27-5)23(29-7)13-19(16)25-3/h10-14,17H,9H2,1-8H3/b15-10+

InChI key

GGIJVVURVQQPBB-XNTDXEJSSA-N

Biochem/physiol Actions

Diasarone-I is an antiviral agent isolated form Acorus tatarinowii Schott that potently inhibits dengue viral infection. Diasarone-I is binds to the viral 2′O methyltransferase of nonstructural protein 5 (NS5). It also decreases the DENV2-induced STAT1 phosphorylation and IFN-stimulated genes (ISGs) expression.
The antiviral effect of Diasarone-I includes half maximal effective concentration (EC50) of 4.5 μM and half maximal cytotoxicity concentration (CC50) of >80 μM.[1]
antiviral agent isolated form Acorus tatarinowii Schott that potently inhibits dengue viral infection

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Xingang Yao et al.
European journal of pharmacology, 821, 11-20 (2017-12-17)
Dengue virus (DENV) is the most prevalent mosquito borne viral pathogen worldwide. However, antiviral drugs against this infection are not available. To identify novel anti-DENV compound from traditional Chinese medicine, we discovered the ethanol extract of Acorus tatarinowii Schott containing
Inhibition of dengue viral infection by diasarone-I is associated with 2'O methyltransferase of NS5
Yao X, et al.
European Journal of Pharmacology, 821, 11-20 (2018)

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