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About This Item
Empirical Formula (Hill Notation):
C13H8O2
CAS Number:
Molecular Weight:
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
Quality Level
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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Storage Class
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| X600-25G | 04061837549809 |