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10470-83-4 | 5,8-QUINOLINEQUINONE
CAS No: 10470-83-4 Catalog No: AG008TXL MDL No:MFCD04038780
Product Description
Catalog Number:
AG008TXL
Chemical Name:
5,8-QUINOLINEQUINONE
CAS Number:
10470-83-4
Molecular Formula:
C9H5NO2
Molecular Weight:
159.1415
MDL Number:
MFCD04038780
IUPAC Name:
quinoline-5,8-dione
InChI:
InChI=1S/C9H5NO2/c11-7-3-4-8(12)9-6(7)2-1-5-10-9/h1-5H
InChI Key:
NVJSPQCVDHGYRE-UHFFFAOYSA-N
SMILES:
O=C1C=CC(=O)c2c1nccc2
NSC Number:
682996
Properties
Complexity:
257
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
159.032g/mol
Formal Charge:
0
Heavy Atom Count:
12
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
159.144g/mol
Monoisotopic Mass:
159.032g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
47A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.7
Literature
| Title | Journal |
|---|---|
| New quinoline-5,8-dione and hydroxynaphthoquinone derivatives inhibit a chloroquine resistant Plasmodium falciparum strain. | European journal of medicinal chemistry 20120801 |
| Application of porous nickel-coated TiO₂ for the photocatalytic degradation of aqueous quinoline in an internal airlift loop reactor. | International journal of environmental research and public health 20120201 |
| 7-Chloro-6-piperidin-1-yl-quinoline-5,8-dione (PT-262), a novel synthetic compound induces lung carcinoma cell death associated with inhibiting ERK and CDC2 phosphorylation via a p53-independent pathway. | Cancer chemotherapy and pharmacology 20081001 |
| The aza-analogues of 1,4-naphthoquinones are potent substrates and inhibitors of plasmodial thioredoxin and glutathione reductases and of human erythrocyte glutathione reductase. | Organic & biomolecular chemistry 20080807 |
| Discovery of quinolinediones exhibiting a heat shock response and angiogenesis inhibition. | Journal of medicinal chemistry 20080424 |
| Investigating the antiproliferative activity of quinoline-5,8-diones and styrylquinolinecarboxylic acids on tumor cell lines. | Bioorganic & medicinal chemistry letters 20071115 |
| Synthesis and in vitro antitumor activity of ring C and D-substituted phenanthrolin-7-one derivatives, analogues of the marine pyridoacridine alkaloids ascididemin and meridine. | Bioorganic & medicinal chemistry 20040801 |
| Antitumor agents. 3. Design, synthesis, and biological evaluation of new pyridoisoquinolindione and dihydrothienoquinolindione derivatives with potent cytotoxic activity. | Journal of medicinal chemistry 20040212 |
| Synthesis and in vitro antitumor activity of novel ring D analogues of the marine pyridoacridine ascididemin: structure-activity relationship. | Journal of medicinal chemistry 20020815 |
| Discovery and biological evaluation of a new family of potent inhibitors of the dual specificity protein phosphatase Cdc25. | Journal of medicinal chemistry 20011122 |
| Synthesis of pyridino[2,3-f]indole-4,9-dione and 6,7-disubstituted quinoline-5,8-dione derivatives and evaluation on their cytotoxic activity. | Bioorganic & medicinal chemistry 20011101 |
| Comparative study on biological activities of heterocyclic quinones and streptonigrin. | The Journal of antibiotics 19870501 |
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