| Weight | 174.155 g/mol |
|---|---|
| Formula | C10H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
juglone (481-39-0)
5-hydroxy-1,4-naphthoquinone
Score:
#1787 in Biochemistry
,
#3908 in Biology
,
#4920 in Chemistry
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- Sigma-Aldrich - juglone53.90 - 172.50 USD
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- TCI - juglone71.00 - 251.00 USD
- 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)
- Cytotoxic Action of Juglone and Plumbagin: A Mechanistic Study Using HaCaT Keratinocytes (Chemical Research in Toxicology, 2004)
- Selective Inactivation of Parvulin-Like Peptidyl-Prolyl cis/trans Isomerases by Juglone (Biochemistry, 1998)
- 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)
- Inhibitory effects of plumbagin and juglone on azoxymethane-induced intestinal carcinogenesis in rats (Cancer Letters, 1998)
- Phenolic Acids, Syringaldehyde, and Juglone in Fruits of Different Cultivars of Juglans regia L. (Journal of Agricultural and Food Chemistry, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-hydroxy-1,4-naphthoquinone
-
SMILESC1=CC2=C(C(=O)C=CC2=O)C(=C1)O
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InChIKeyKQPYUDDGWXQXHS-UHFFFAOYSA-N
- Pubchem - juglone
- Wikipedia - juglone
Juglone, also called 5-hydroxy-1,4-naphthalenedione (IUPAC) is an organic compound with the molecular formula C10H6O3. In the food industry, juglone is also known as C.I. Natural Brown 7 and C.I.
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juglone
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