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Merck
CN

X600

呫吨酮

97%

别名:

氧杂蒽酮

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关于此项目

经验公式(希尔记法):
C13H8O2
化学文摘社编号:
分子量:
196.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-997-7
Beilstein/REAXYS Number:
140443
MDL number:
Assay:
97%
Form:
powder
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产品名称

呫吨酮, 97%

InChI key

JNELGWHKGNBSMD-UHFFFAOYSA-N

InChI

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

SMILES string

O=C1c2ccccc2Oc3ccccc13

assay

97%

form

powder

bp

349-350 °C/730 mmHg (lit.)

mp

172-174 °C (lit.)

Quality Level

Gene Information

mouse ... Prkch(18755)

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存储类别

11 - Combustible Solids

wgk

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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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
Yann Fromentin et al.
Organic letters, 14(19), 5054-5057 (2012-09-19)
Benzoylphloroglucinol derivatives are natural products showing diverse biological activities that could be modulated by structural modifications. For this purpose, we studied the biotransformation of guttiferone A and of maclurin using a combinatorial approach for screening active microorganism strains. We found
Ruttiros Khonkarn et al.
Colloids and surfaces. B, Biointerfaces, 94, 266-273 (2012-03-02)
Xanthone exhibits several medicinal activities and especially it inhibits the growth of cancer cells. However, the use of xanthone is limited because of its low aqueous solubility and systemic toxicity. In the present study xanthone was loaded into poly(ethylene glycol)-b-poly[N-(2-hydroxypropyl)
Ibrahim Jantan et al.
Phytochemistry, 80, 58-63 (2012-05-30)
Three benzophenones, 2,6,3',5'-tetrahydroxybenzophenone (1), 3,4,5,3',5'-pentahydroxybenzophenone (3) and 3,5,3',5'-tetrahydroxy-4-methoxybenzophenone (4), as well as a xanthone, 1,3,6-trihydroxy-5-methoxy-7-(3'-methyl-2'-oxo-but-3'-enyl)xanthone (9), were isolated from the twigs of Garcinia cantleyana var. cantleyana. Eight known compounds, 3,4,5,3'-tetrahydroxy benzophenone (2), 1,3,5-trihydroxyxanthone (5), 1,3,8-trihydroxyxanthone (6), 2,4,7-trihydroxyxanthone (7), 1,3,5,7-tetrahydroxyxanthone (8)
Kavitha Sudheendran et al.
The Journal of organic chemistry, 77(22), 10194-10210 (2012-10-17)
As little as 0.5 mol % CuCl is sufficient to catalyze the intramolecular O-arylation of easily accessible 2-(2-bromobenzyl)cyclohexane-1,3-diones to provide the corresponding 2,3,4,9-tetrahydro-1H-xanthen-1-ones with yields ranging from 83% to 99%.

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