Drug Information
Drug General Information | Top | |||
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Drug ID |
D0R1EO
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Former ID |
DNC012535
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Drug Name |
[3-(Biphenyl-4-yloxy)-propyl]-dimethyl-amine
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Synonyms |
CHEMBL132091; [3-(Biphenyl-4-yloxy)-propyl]-dimethyl-amine; N,N-dimethyl-3-(4-phenylphenoxy)propan-1-amine; AC1L9UWB; SCHEMBL10679594; ZINC4842179; BDBM50133286
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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 |
C17H21NO
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Canonical SMILES |
CN(C)CCCOC1=CC=C(C=C1)C2=CC=CC=C2
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InChI |
1S/C17H21NO/c1-18(2)13-6-14-19-17-11-9-16(10-12-17)15-7-4-3-5-8-15/h3-5,7-12H,6,13-14H2,1-2H3
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InChIKey |
ITTYRYJIHNHJBL-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Lanosterol synthase (LSS) | Target Info | Inhibitor | [1] |
BioCyc | Cholesterol biosynthesis II (via 24,25-dihydrolanosterol) | |||
Cholesterol biosynthesis III (via desmosterol) | ||||
Cholesterol biosynthesis I | ||||
Superpathway of cholesterol biosynthesis | ||||
Lanosterol biosynthesis | ||||
KEGG Pathway | Steroid biosynthesis | |||
Metabolic pathways | ||||
Biosynthesis of antibiotics | ||||
Panther Pathway | Cholesterol biosynthesis | |||
Pathwhiz Pathway | Steroid Biosynthesis | |||
Reactome | Cholesterol biosynthesis | |||
Activation of gene expression by SREBF (SREBP) | ||||
WikiPathways | Activation of Gene Expression by SREBP (SREBF) | |||
SREBP signalling | ||||
Cholesterol Biosynthesis | ||||
Cholesterol biosynthesis |
References | Top | |||
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REF 1 | Oxidosqualene cyclase inhibitors as antimicrobial agents. J Med Chem. 2003 Sep 25;46(20):4240-3. |
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