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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
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
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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