Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D06CWX
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| Former ID |
DNC011467
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| Drug Name |
1-Hydroxy-8-methoxy-10H-anthracen-9-one
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| Synonyms |
CHEMBL125592; 9(10H)-Anthracenone, 1-hydroxy-8-methoxy-; 138591-01-2; ACMC-20mxto; 1-Hydroxy-8-methoxy-10H-anthracen-9-one; 1-Hydroxy-8-methoxyanthrone; SCHEMBL12775753; CTK0B8005; DTXSID10568303; ZINC13366515; BDBM50060886; AKOS030561671
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
 |
Download2D MOL |
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| Formula |
C15H12O3
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| Canonical SMILES |
COC1=CC=CC2=C1C(=O)C3=C(C2)C=CC=C3O
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| InChI |
1S/C15H12O3/c1-18-12-7-3-5-10-8-9-4-2-6-11(16)13(9)15(17)14(10)12/h2-7,16H,8H2,1H3
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| InChIKey |
KXNCIFRRMSGNPW-UHFFFAOYSA-N
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| CAS Number |
CAS 138591-01-2
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Arachidonate 5-lipoxygenase (5-LOX) | Target Info | Inhibitor | [1] |
| BioCyc | Aspirin-triggered lipoxin biosynthesis | |||
| Resolvin D biosynthesis | ||||
| Leukotriene biosynthesis | ||||
| Lipoxin biosynthesis | ||||
| Aspirin triggered resolvin D biosynthesis | ||||
| Aspirin triggered resolvin E biosynthesis | ||||
| KEGG Pathway | Arachidonic acid metabolism | |||
| Metabolic pathways | ||||
| Serotonergic synapse | ||||
| Ovarian steroidogenesis | ||||
| Toxoplasmosis | ||||
| NetPath Pathway | IL4 Signaling Pathway | |||
| Pathwhiz Pathway | Arachidonic Acid Metabolism | |||
| WikiPathways | Vitamin D Receptor Pathway | |||
| Arachidonic acid metabolism | ||||
| Eicosanoid Synthesis | ||||
| Selenium Micronutrient Network | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Simple analogues of anthralin: unusual specificity of structure and antiproliferative activity. J Med Chem. 1997 Nov 7;40(23):3773-80. | |||
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