CAS 129-39-5: 1,8-Dinitro-9,10-anthracenedione
Formula:C14H6N2O6
InChI:InChI=1S/C14H6N2O6/c17-13-7-3-1-5-9(15(19)20)11(7)14(18)12-8(13)4-2-6-10(12)16(21)22/h1-6H
InChI key:InChIKey=MBIJFIUDKPXMAV-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)C=3C1=C(N(=O)=O)C=CC3)=CC=CC2N(=O)=O
Synonyms:- 1,8-Dinitro-9,10-anthracenedione
- 1,8-Dinitro-9,10-anthraquinone
- 9,10-Anthracenedione, 1,8-dinitro-
- 9,10-Anthracenedione, 1,8-dinitro-1,8-dinitroanthracene-9,10-dione
- Alizarine Violet R Base
- Anthraquinone, 1,8-dinitro-
- NSC 37108
- Waxoline Violet BA
- C.I. Solvent Violet 14
- 1,8-Dinitroanthraquinone
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Found 4 products.
9,10-Anthracenedione, 1,8-dinitro-
CAS:Formula:C14H6N2O6Purity:96%Color and Shape:SolidMolecular weight:298.20723999999991,8-Dinitroanthraquinone
CAS:1,8-DinitroanthraquinoneFormula:C14H6N2O6Purity:95%Color and Shape: yellow crystalline solidMolecular weight:298.21g/mol1,8-Dinitroanthraquinone
CAS:1,8-Dinitroanthraquinone is an aromatic hydrocarbon that inhibits the growth of bacteria in vitro. This compound has been shown to inhibit telomerase activity and to be a potent inhibitor of monosodium glutamate-induced nitrosative stress in cultured cells. It also inhibits nitrite ion reduction by 2-phenylbutyric acid, which is an acceptor for the nitrite ion. 1,8-Dinitroanthraquinone has been shown to have a kinetic effect on the conversion of nitrite ion to nitrous acid, which is important in the formation of carcinogenic nitrosamines. The paradigm shift in this research was that the inhibition of telomerase activity was not only due to its effects on DNA but also due to its activation energy as well as its effects on protein synthesis.Formula:C14H6N2O6Purity:Min. 96 Area-%Color and Shape:PowderMolecular weight:298.21 g/mol1,8-Dinitroanthraquinone
CAS:Controlled ProductFormula:C14H6N2O6Color and Shape:NeatMolecular weight:298.21
