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Y0001611

Esculetin

European Pharmacopoeia (EP) Reference Standard

Sinonimo/i:

6,7-Dihydroxycoumarin, Cichorigenin, Esculetin

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About This Item

Formula empirica (notazione di Hill):
C9H6O4
Numero CAS:
305-01-1
Peso molecolare:
178.14
Beilstein:
152788
Numero MDL:
MFCD00006874
Codice UNSPSC:
41116107
ID PubChem:
329831510
NACRES:
NA.24

Grado

pharmaceutical primary standard

Famiglia di API

esculetin

Produttore/marchio commerciale

EDQM

Punto di fusione

271-273 °C (lit.)

applicazioni

pharmaceutical (small molecule)

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

Oc1cc2OC(=O)C=Cc2cc1O

InChI

1S/C9H6O4/c10-6-3-5-1-2-9(12)13-8(5)4-7(6)11/h1-4,10-11H
ILEDWLMCKZNDJK-UHFFFAOYSA-N

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Descrizione generale

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Applicazioni

Esculetin EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Confezionamento

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Altre note

Sales restrictions may apply.

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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Lot/Batch Number

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Sigma-Aldrich

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Sigma-Aldrich

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Rashi Arora et al.
Molecular cancer, 15(1), 64-64 (2016-10-21)
A handful of studies have exploited antitumor potential of esculetin, a dihydroxy coumarine derivative; the targets to which it binds and the possible downstream mechanism for its cytotoxicity in cancer cells remain to be elucidated. Using pancreatic cancer cell lines
Edson Luis Maistro et al.
Journal of toxicology and environmental health. Part A, 78(2), 109-118 (2014-11-27)
Coumarins are naturally occurring compounds, widely distributed throughout the plant kingdom (Plantae), and possess important pharmacological properties, including inhibition of oxidative stress. In this context, newly synthesized coumarin compounds are being produced due to their potent antioxidant activities. Therefore, the
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Yoon-Young Sung et al.
Environmental toxicology and pharmacology, 38(1), 41-50 (2014-06-01)
Viola mandshurica W. Becker has been used as an expectorant, diuretic, and anti-inflammatory agent. We evaluated the effects of V. mandshurica ethanol extract (VME) on high-fat-diet (HFD)-induced obesity in mice. HPLC analysis showed that the VME contained 11.95 ± 0.37
Oussama Ahrazem et al.
Plant science : an international journal of experimental plant biology, 234, 60-73 (2015-03-26)
Glycosyltransferases play diverse roles in cellular metabolism by modifying the activities of regulatory metabolites. Three stress-regulated UDP-glucosyltransferase-encoding genes have been isolated from the stigmas of saffron, UGT85U1, UGT85U2 and UGT85V1, which belong to the UGT85 family that includes members associated

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