Drug General Information |
Drug ID |
D06HFV
|
Former ID |
DNC005627
|
Drug Name |
5-[5-Fluoro-indan-(1E)-ylidenemethyl]-pyrimidine
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
Download
2D MOL
3D MOL
|
Formula |
C14H11FN2
|
Canonical SMILES |
C1CC(=CC2=CN=CN=C2)C3=C1C=C(C=C3)F
|
InChI |
1S/C14H11FN2/c15-13-3-4-14-11(1-2-12(14)6-13)5-10-7-16-9-17-8-10/h3-9H,1-2H2/b11-5+
|
InChIKey |
LEJPKWXGQFBXRX-VZUCSPMQSA-N
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PubChem Compound ID |
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Target and Pathway |
Target(s) |
Cytochrome P450 19 |
Target Info |
Inhibitor |
[1]
|
17 alpha-hydroxylase-C17, 20-lyase |
Target Info |
Inhibitor |
[1]
|
Cytochrome P450 11B1, mitochondrial |
Target Info |
Inhibitor |
[1]
|
BioCyc Pathway
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Superpathway of steroid hormone biosynthesis
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Estradiol biosynthesis II
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Estradiol biosynthesis IPWY-7305:Superpathway of steroid hormone biosynthesis
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Glucocorticoid biosynthesis
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Androgen biosynthesisPWY-7305:Superpathway of steroid hormone biosynthesis
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Mineralocorticoid biosynthesis
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KEGG Pathway
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Steroid hormone biosynthesis
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Metabolic pathways
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Ovarian steroidogenesishsa00140:Steroid hormone biosynthesis
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Ovarian steroidogenesis
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Prolactin signaling pathwayhsa00140:Steroid hormone biosynthesis
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NetPath Pathway
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FSH Signaling Pathway
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PANTHER Pathway
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Androgen/estrogene/progesterone biosynthesis
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PathWhiz Pathway
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Androgen and Estrogen MetabolismPW000045:Androgen and Estrogen Metabolism
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SteroidogenesisPW000141:Steroidogenesis
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Reactome
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Endogenous sterolsR-HSA-193048:Androgen biosynthesis
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Glucocorticoid biosynthesis
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Endogenous sterolsR-HSA-194002:Glucocorticoid biosynthesis
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Endogenous sterols
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WikiPathways
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Metapathway biotransformation
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Tryptophan metabolism
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Oxidation by Cytochrome P450
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Ovarian Infertility Genes
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Metabolism of steroid hormones and vitamin D
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FSH signaling pathway
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Integrated Breast Cancer Pathway
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Phase 1 - Functionalization of compoundsWP702:Metapathway biotransformation
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Steroid Biosynthesis
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Glucocorticoid & Mineralcorticoid Metabolism
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Prostate Cancer
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Corticotropin-releasing hormone
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References |
REF 1 | J Med Chem. 2005 Mar 10;48(5):1563-75.Synthesis and evaluation of (pyridylmethylene)tetrahydronaphthalenes/-indanes and structurally modified derivatives: potent and selective inhibitors of aldosterone synthase. |