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	[532449]
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
PubChem Compound ID	5490028
Target and Pathway
Target(s)	17 alpha-hydroxylase-C17, 20-lyase	Target Info	Inhibitor	[532449]
	3-oxo-5-alpha-steroid 4-dehydrogenase 2	Target Info	Inhibitor	[532449]
	3-oxo-5-alpha-steroid 4-dehydrogenase 1	Target Info	Inhibitor	[532449]
BioCyc Pathway	Superpathway of steroid hormone biosynthesis
	Glucocorticoid biosynthesis
	Androgen biosynthesisPWY-7305:Superpathway of steroid hormone biosynthesis
	Allopregnanolone biosynthesis
	Androgen biosynthesis
KEGG Pathway	Steroid hormone biosynthesis
	Metabolic pathways
	Ovarian steroidogenesis
	Prolactin signaling pathwayhsa00140:Steroid hormone biosynthesis
	Prostate cancerhsa00140:Steroid hormone biosynthesis
NetPath Pathway	IL2 Signaling Pathway
PathWhiz Pathway	Androgen and Estrogen Metabolism
	SteroidogenesisPW000045:Androgen and Estrogen Metabolism
Reactome	Androgen biosynthesis
	Glucocorticoid biosynthesis
	Endogenous sterolsR-HSA-193048:Androgen biosynthesisR-HSA-193048:Androgen biosynthesis
WikiPathways	Metapathway biotransformation
	Steroid Biosynthesis
	Oxidation by Cytochrome P450
	Metabolism of steroid hormones and vitamin D
	Glucocorticoid & Mineralcorticoid Metabolism
	Prostate Cancer
	Phase 1 - Functionalization of compounds
References
Ref 532449	J Med Chem. 1990 Sep;33(9):2452-5.Hydroxyperfluoroazobenzenes: novel inhibitors of enzymes of androgen biosynthesis.
Ref 532449	J Med Chem. 1990 Sep;33(9):2452-5.Hydroxyperfluoroazobenzenes: novel inhibitors of enzymes of androgen biosynthesis.

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