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51773

Supelco

Desmethoxyyangonin

analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C14H12O3
Numero CAS:
15345-89-8
Peso molecolare:
228.24
Beilstein:
181238
Numero MDL:
MFCD00221730
Codice UNSPSC:
85151701
ID PubChem:
329757739
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥95.0% (HPLC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Impurezze

≤5.0% water

applicazioni

food and beverages

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

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+
DKKJNZYHGRUXBS-BQYQJAHWSA-N

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Applicazioni

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

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
BCBW8522
BCBM7271V
BCBH0920V
BCBH0920

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[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)
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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
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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