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Y0001611

Esculetin

European Pharmacopoeia (EP) Reference Standard

Synonim(y):

6,7-Dihydroxycoumarin, Cichorigenin, Esculetin

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About This Item

Wzór empiryczny (zapis Hilla):
C9H6O4
Numer CAS:
305-01-1
Masa cząsteczkowa:
178.14
Beilstein:
152788
Numer MDL:
MFCD00006874
Kod UNSPSC:
41116107
Identyfikator substancji w PubChem:
329831510
NACRES:
NA.24

klasa czystości

pharmaceutical primary standard

rodzina API

esculetin

producent / nazwa handlowa

EDQM

mp

271-273 °C (lit.)

Zastosowanie

pharmaceutical (small molecule)

format

neat

temp. przechowywania

2-8°C

ciąg SMILES

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

Klucz InChI

ILEDWLMCKZNDJK-UHFFFAOYSA-N

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Opis ogólny

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.

Zastosowanie

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

Opakowanie

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

Inne uwagi

Sales restrictions may apply.
This page may contain text that has been machine translated.

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Choose from one of the most recent versions:

Certyfikaty analizy (CoA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

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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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