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Key Documents

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X600

Sigma-Aldrich

Xanthone

97%

Sinónimos:

9-Xanthenone

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About This Item

Fórmula empírica (notación de Hill):
C13H8O2
Número de CAS:
90-47-1
Peso molecular:
196.20
Beilstein/REAXYS Number:
140443
EC Number:
201-997-7
MDL number:
MFCD00005060
UNSPSC Code:
12352100
PubChem Substance ID:
24902151
NACRES:
NA.22

Quality Level

100

assay

97%

form

powder

bp

349-350 °C/730 mmHg (lit.)

mp

172-174 °C (lit.)

SMILES string

O=C1c2ccccc2Oc3ccccc13

InChI

1S/C13H8O2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1-8H

InChI key

JNELGWHKGNBSMD-UHFFFAOYSA-N

Gene Information

mouse ... Prkch(18755)

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Categorías relacionadas

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
STBK6196
STBJ1709
STBH7013
STBH1916
STBH0923

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Thioxanthone European Pharmacopoeia (EP) Reference Standard

T1305000

Thioxanthone

Rajan Giri et al.
Bioorganic & medicinal chemistry, 18(4), 1456-1463 (2010-02-05)
A series of substituted xanthenes was synthesized and screened for activity using DU-145, MCF-7, and HeLa cancer cell growth inhibition assays. The most potent compound, 9 g ([N,N-diethyl]-9-hydroxy-9-(3-methoxyphenyl)-9H-xanthene-3-carboxamide), was found to inhibit cancer cell growth with IC(50) values ranging from
Asako Murata et al.
Bioorganic & medicinal chemistry letters, 23(1), 252-255 (2012-11-21)
In recent years, various biological processes have been found to be regulated by miRNA-mediated gene silencing. A small molecule that modulate the miRNA pathway will provide the biological tool for elucidating mechanisms of miRNA-mediated gene regulation, and can be the
Krishna Kanta Ghosh et al.
Chemical communications (Cambridge, England), 47(26), 7488-7490 (2011-06-02)
We report the first solid phase synthesis of a xanthone library CX and its application to embryonic stem cell probe development. The CX library was further derivatised with an activated ester resin to provide an acetylated CX (CXAC) library. Screening
Michael A Schätzle et al.
Journal of the American Chemical Society, 134(36), 14742-14745 (2012-08-23)
Reduction of emodin by sodium dithionite resulted in the formation of two tautomeric forms of emodin hydroquinone. Subsequent conversion by the short-chain dehydrogenase/reductase (SDR) MdpC into the corresponding 3-hydroxy-3,4-dihydroanthracen-1(2H)-one implies that deoxygenation is the first step in monodictyphenone biosynthesis. Implications
Jessie A Blake et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 11(3), 539-547 (2012-01-10)
We have attached the antiviral drug acyclovir (ACV) to a xanthone photolabile protecting group (or photocage) through the O6 position of acyclovir, a procedure designed for the treatment of ocular herpes simplex virus infections. Acyclovir is photoreleased from the photocage
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