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51773

Supelco

Desmethoxyyangonin

analytical standard

Sinónimos:

(E)-4-Methoxy-6-(2-phenylethenyl)-2H-pyran-2-one, 5,6-Dehydrokavain, Demethoxyyangonin

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About This Item

Fórmula empírica (notación de Hill):
C14H12O3
Número de CAS:
15345-89-8
Peso molecular:
228.24
Beilstein/REAXYS Number:
181238
MDL number:
MFCD00221730
UNSPSC Code:
85151701
PubChem Substance ID:
329757739
NACRES:
NA.24

grade

analytical standard

Quality Level

100

assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤5.0% water

application(s)

food and beverages

format

neat

storage temp.

2-8°C

SMILES string

COC1=CC(=O)OC(\C=C\c2ccccc2)=C1

InChI

1S/C14H12O3/c1-16-13-9-12(17-14(15)10-13)8-7-11-5-3-2-4-6-11/h2-10H,1H3/b8-7+

InChI key

DKKJNZYHGRUXBS-BQYQJAHWSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificados de análisis (COA)

Lot/Batch Number
BCBW8522

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Yen Thi-Kim Nguyen et al.
Molecules (Basel, Switzerland), 24(12) (2019-06-21)
Pavetta indica L. is used in traditional medicine for the treatment of various diseases including hemorrhoids, headache, urinary conditions, ulcerated nose, and dropsy. However, no study has evaluated the anticancer effect of P. indica L. In this study, we found
[Effects of the constituents of Alpinia speciosa rhizoma on experimental ulcers].
S Y Hsu
Taiwan yi xue hui za zhi. Journal of the Formosan Medical Association, 86(1), 58-64 (1987-01-01)
Atul Upadhyay et al.
Journal of agricultural and food chemistry, 59(7), 2857-2862 (2011-02-11)
AIDS and influenza are viral pandemics and remain one of the leading causes of human deaths worldwide. The increasing resistance of these diseases to synthetic drugs demands the search for novel compounds from plant-based sources. In this regard, the leaves
C M Teng et al.
The Chinese journal of physiology, 33(1), 41-48 (1990-01-01)
5,6-Dehydrokawain (DK) and dihydro-5,6-dehydrokawain (DDK) inhibited the aggregation and ATP release of rabbit platelets induced by arachidonic acid and collagen, without affecting those induced by ADP, PAF and thrombin. This inhibition was reversible and in a concentration-dependent manner. The IC50
I Jantan et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 15(4), 306-309 (2007-10-05)
Twelve compounds isolated from Alpinia mutica Roxb., Kaempferia rotunda Linn., Curcuma xanthorhiza Roxb., Curcuma aromatica Valeton and Zingiber zerumbet Smith (Family: Zingiberaceae) and three synthesized derivatives of xanthorrhizol were evaluated for their ability to inhibit arachidonic acid- (AA), collagen- and
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