Drug General Information |
Drug ID |
D07ZNR
|
Former ID |
DNC011674
|
Drug Name |
2,3,5,6-Tetrafluoro-4-pentafluorophenylazo-phenol
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
Download
2D MOL
3D MOL
|
Formula |
C12HF9N2O
|
Canonical SMILES |
C1(=C(C(=C(C(=C1F)F)F)F)F)NN=C2C(=C(C(=O)C(=C2F)F)F)F
|
InChI |
1S/C12HF9N2O/c13-1-2(14)4(16)10(5(17)3(1)15)22-23-11-6(18)8(20)12(24)9(21)7(11)19/h22H
|
InChIKey |
FNPGFLBPXIANTH-UHFFFAOYSA-N
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PubChem Compound ID |
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Target and Pathway |
Target(s) |
17 alpha-hydroxylase-C17, 20-lyase |
Target Info |
Inhibitor |
[1]
|
3-oxo-5-alpha-steroid 4-dehydrogenase 2 |
Target Info |
Inhibitor |
[1]
|
3-oxo-5-alpha-steroid 4-dehydrogenase 1 |
Target Info |
Inhibitor |
[1]
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BioCyc Pathway
|
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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Allopregnanolone biosynthesis
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Androgen 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 steroidogenesis
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Prolactin signaling pathwayhsa00140:Steroid hormone biosynthesis
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Prostate cancerhsa00140:Steroid hormone biosynthesis
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NetPath Pathway
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IL2 Signaling Pathway
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PathWhiz Pathway
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Androgen and Estrogen Metabolism
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SteroidogenesisPW000045:Androgen and Estrogen Metabolism
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Reactome
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Androgen biosynthesis
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Glucocorticoid biosynthesis
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Endogenous sterolsR-HSA-193048:Androgen biosynthesisR-HSA-193048:Androgen biosynthesis
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WikiPathways
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Metapathway biotransformation
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Steroid Biosynthesis
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Oxidation by Cytochrome P450
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Metabolism of steroid hormones and vitamin D
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Glucocorticoid & Mineralcorticoid Metabolism
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Prostate Cancer
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Phase 1 - Functionalization of compounds
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References |
REF 1 | J Med Chem. 1990 Sep;33(9):2452-5.Hydroxyperfluoroazobenzenes: novel inhibitors of enzymes of androgen biosynthesis. |