Weight | 158.156 g/mol |
---|---|
Formula | C10H6O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
1,2-NAPHTHOQUINONE (524-42-5)
ortho-naphthoquinone · o-naphthoquinone
Score:
#721 in Biochemistry
,
#2439 in Chemistry
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- The metabolism of menadione (2-methyl-1,4-naphthoquinone) by isolated hepatocytes. A study of the implications of oxidative stress in intact cells. (Journal of Biological Chemistry, 1982)
- Site of action of the antimalarial hydroxynaphthoquinone, 2-[trans-4-(4'-chlorophenyl) cyclohexyl]-3- hydroxy-1,4-naphthoquinone (566C80) (Biochemical Pharmacology, 1992)
- Formation and reduction of glutathione-protein mixed disulfides during oxidative stress: A study with isolated hepatocytes and menadione (2-methyl-1,4-naphthoquinone) (Biochemical Pharmacology, 1987)
- Plumbagin (5-Hydroxy-2-methyl-1,4-naphthoquinone) Suppresses NF-B Activation and NF-B-regulated Gene Products Through Modulation of p65 and IB Kinase Activation, Leading to Potentiation of Apoptosis Induced by Cytokine and Chemotherapeutic Agents (Journal of Biological Chemistry, 2006)
- 2-and 3-substituted 1,4-naphthoquinone derivatives as subversive substrates of trypanothione reductase and lipoamide dehydrogenase from Trypanosoma cruzi: Synthesis and correlation between redox cycling activities and in vitro cytotoxicity (Journal of Medicinal Chemistry, 2001)
- Plumbagin (5-Hydroxy-2-methyl-1,4-naphthoquinone) Induces Apoptosis and Cell Cycle Arrest in A549 Cells through p53 Accumulation via c-Jun NH2-Terminal Kinase-Mediated Phosphorylation at Serine 15 in Vitro and in Vivo (Journal of Pharmacology and Experimental Therapeutics, 2006)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - ortho-naphthoquinone
- o-naphthoquinone
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SMILESC1=CC=C2C(=C1)C=CC(=O)C2=O
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InChIKeyKETQAJRQOHHATG-UHFFFAOYSA-N
- Pubchem - 1,2-NAPHTHOQUINONE
- Wikipedia - 1,2-naphthoquinone
1,2-Naphthoquinone or ortho-naphthoquinone is a polycyclic aromatic organic compound with formula C 10H 6O 2. This double ketone (quinone) is a reactive metabolite of naphthalene and is found in diesel exhaust particles. The accumulation of this toxic metabolite in rats from doses of naphthalene has been shown to cause eye damage, including the formation of cataracts.
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