General Information of Drug Therapeutic Target (DTT) (ID: TTRA5BZ)

DTT Name Steroid 17-alpha-monooxygenase (S17AH)
Synonyms Steroid 17-alpha-hydroxylase/17,20 lyase; P450c17; P450-C17; P450 17; CYPXVII; CYP17A1; CYP 17; 17 alpha-Hydroxylase/C17-20-lyase
Gene Name CYP17A1
DTT Type
Successful target
[1]
BioChemical Class
Paired donor oxygen oxidoreductase
UniProt ID
CP17A_HUMAN
TTD ID
T89041
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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EC Number
EC 1.14.14.19
Sequence
MWELVALLLLTLAYLFWPKRRCPGAKYPKSLLSLPLVGSLPFLPRHGHMHNNFFKLQKKY
GPIYSVRMGTKTTVIVGHHQLAKEVLIKKGKDFSGRPQMATLDIASNNRKGIAFADSGAH
WQLHRRLAMATFALFKDGDQKLEKIICQEISTLCDMLATHNGQSIDISFPVFVAVTNVIS
LICFNTSYKNGDPELNVIQNYNEGIIDNLSKDSLVDLVPWLKIFPNKTLEKLKSHVKIRN
DLLNKILENYKEKFRSDSITNMLDTLMQAKMNSDNGNAGPDQDSELLSDNHILTTIGDIF
GAGVETTTSVVKWTLAFLLHNPQVKKKLYEEIDQNVGFSRTPTISDRNRLLLLEATIREV
LRLRPVAPMLIPHKANVDSSIGEFAVDKGTEVIINLWALHHNEKEWHQPDQFMPERFLNP
AGTQLISPSVSYLPFGAGPRSCIGEILARQELFLIMAWLLQRFDLEVPDDGQLPSLEGIP
KVVFLIDSFKVKIKVRQAWREAQAEGST
Function
Conversion of pregnenolone and progesterone to their 17- alpha-hydroxylated products and subsequently to dehydroepiandrosterone (DHEA) and androstenedione. Catalyzes both the 17-alpha-hydroxylation and the 17,20-lyase reaction. Involved in sexual development during fetal life and at puberty.
KEGG Pathway
Steroid hormone biosynthesis (hsa00140 )
Metabolic pathways (hsa01100 )
Ovarian steroidogenesis (hsa04913 )
Prolactin signaling pathway (hsa04917 )
Reactome Pathway
Glucocorticoid biosynthesis (R-HSA-194002 )
Endogenous sterols (R-HSA-211976 )
Androgen biosynthesis (R-HSA-193048 )
BioCyc Pathway
MetaCyc:HS07560-MON

Molecular Interaction Atlas (MIA) of This DTT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DTT
2 Approved Drug(s) Targeting This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
ABIRATERONE DM8V75C Prostate cancer 2C82.0 Approved [1]
Abiraterone acetate DMANBZI Prostate cancer 2C82.0 Approved [2]
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5 Clinical Trial Drug(s) Targeting This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
TAK-700 DM2H8FZ Prostate cancer 2C82.0 Phase 3 [3]
TAVT-45 DMHBRGT Prostate cancer 2C82.0 Phase 3 [4]
Seviteronel DM9IMEZ Breast cancer 2C60-2C65 Phase 2 [5]
CFG920 DM2BXDU Prostate cancer 2C82.0 Phase 1/2 [6]
DST-2970 DM69ZBU Prostate cancer 2C82.0 Phase 1 [7]
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89 Investigative Drug(s) Targeting This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
1-((9H-Fluoren-2-yl)ethyl)-1H-imidazole DMGRV8U Discovery agent N.A. Investigative [8]
1-((9H-Fluoren-2-yl)methyl)-1H-imidazole DMPBJ9L Discovery agent N.A. Investigative [8]
1-(1-(4'-Ethylbiphenyl-4-yl)propyl)-1H-imidazole DMOQPKT Discovery agent N.A. Investigative [8]
1-(1-(4-thiophen-3-yl-phenyl)propyl)-1Himidazole DMQF2N5 Discovery agent N.A. Investigative [9]
1-(1-(4-thiophen-3-ylphenyl)ethyl)-1H-imidazole DMEIH5N Discovery agent N.A. Investigative [9]
1-(1-(Biphenyl-4-yl)allyl)-1H-imidazole DMLJ7WA Discovery agent N.A. Investigative [8]
1-(1-Biphenyl-4-yl-2-methyl-propyl)-1H-imidazole DMPEIQT Discovery agent N.A. Investigative [8]
1-(1-Biphenyl-4-yl-2-phenyl-ethyl)-1H-imidazole DMCTF8X Discovery agent N.A. Investigative [8]
1-(1-Biphenyl-4-yl-3-methyl-butyl)-1H-imidazole DMWME7I Discovery agent N.A. Investigative [8]
1-(1-Biphenyl-4-yl-butyl)-1H-imidazole DM4XILF Discovery agent N.A. Investigative [8]
1-(1-Biphenyl-4-yl-ethyl)-1H-imidazole DMW85CH Discovery agent N.A. Investigative [8]
1-(1-Biphenyl-4-yl-pentyl)-1H-imidazole DM3AD7E Discovery agent N.A. Investigative [8]
1-(1-Biphenyl-4-yl-propyl)-1H-imidazole DMGVE3F Discovery agent N.A. Investigative [8]
1-(3,4-dichlorobenzyl)-1H-imidazole DMX6PKO Discovery agent N.A. Investigative [10]
1-(3,4-difluorobenzyl)-1H-imidazole DMRXD2P Discovery agent N.A. Investigative [10]
1-(3,5-bis(trifluoromethyl)benzyl)-1H-imidazole DM5WOK8 Discovery agent N.A. Investigative [10]
1-(3,5-dibromobenzyl)-1H-imidazole DMNRCM0 Discovery agent N.A. Investigative [10]
1-(3,5-dichlorobenzyl)-1H-imidazole DMLSWHP Discovery agent N.A. Investigative [10]
1-(3,5-difluorobenzyl)-1H-imidazole DMEAI6V Discovery agent N.A. Investigative [10]
1-(3-(4-chlorophenyl)propyl)-1H-imidazole DMIFARP Discovery agent N.A. Investigative [11]
1-(3-(4-fluorophenyl)propyl)-1H-imidazole DMWKXZ2 Discovery agent N.A. Investigative [11]
1-(3-phenylpropyl)-1H-imidazole DMPAWFJ Discovery agent N.A. Investigative [11]
1-(4-Bromobenzyl)-1H-imidazole DM2C7U0 Discovery agent N.A. Investigative [11]
1-(4-bromophenethyl)-1H-imidazole DME8B15 Discovery agent N.A. Investigative [11]
1-(4-chlorobenzyl)-1H-imidazole DMBR9TQ Discovery agent N.A. Investigative [11]
1-(4-chlorophenethyl)-1H-imidazole DM9MDZG Discovery agent N.A. Investigative [11]
1-(4-fluorobenzyl)-1H-imidazole DMBJCGA Discovery agent N.A. Investigative [11]
1-(4-iodobenzyl)-1H-imidazole DMM17I0 Discovery agent N.A. Investigative [12]
1-(4-methyl-benzyl)-1H-imidazole DM48ISZ Discovery agent N.A. Investigative [10]
1-(4-nitrobenzyl)-1H-imidazole DMKT2MB Discovery agent N.A. Investigative [10]
1-(Bis-biphenyl-4-yl-methyl)-1H-imidazole DMF3D5R Discovery agent N.A. Investigative [8]
1-Ethyl-5-(imidazol-1-yl-phenyl-methyl)-1H-indole DMUOSJG Discovery agent N.A. Investigative [13]
1-Imidazol-1-ylmethyl-4-nitro-xanthen-9-one DMN7KHS Discovery agent N.A. Investigative [14]
1-Imidazol-1-ylmethylxanthen-9-one DMIDX7P Discovery agent N.A. Investigative [15]
2,3,4,5-Tetrafluoro-6-pentafluorophenylazo-phenol DMGQE4B Discovery agent N.A. Investigative [16]
2,3,5,6-Tetrafluoro-4-pentafluorophenylazo-phenol DMRVYKQ Discovery agent N.A. Investigative [16]
2-(1-Imidazol-1-yl-ethyl)-9H-carbazole DM4MIXK Discovery agent N.A. Investigative [8]
3-(1-Chloro-7-methoxy-naphthalen-2-yl)-pyridine DMLH7YI Discovery agent N.A. Investigative [17]
3-(1-ethyl-3,4-dihydronaphthalen-2-yl)-pyridine DMR7M82 Discovery agent N.A. Investigative [18]
3-(1-methyl-3,4-dihydronaphthalen-2-yl)-pyridine DMU5HMC Discovery agent N.A. Investigative [18]
3-(6-Ethoxy-naphthalen-2-yl)-pyridine DMUQ0WI Discovery agent N.A. Investigative [17]
3-(6-methoxy-3,4-dihydronaphthalen-2-yl)pyridine DMAJHXO Discovery agent N.A. Investigative [18]
3-(6-methoxynaphthalen-2-yl)pyridine DMYRJAB Discovery agent N.A. Investigative [19]
3-fluoro-4'-(1-(pyridin-4-yl)propyl)biphenyl-4-ol DM4PLSU Discovery agent N.A. Investigative [20]
3-Fluoro-4'-(pyridin-4-ylmethyl)biphenyl-4-ol DMJ3WNP Discovery agent N.A. Investigative [21]
3-[(4'-Hydroxybiphenyl-4-yl)methyl]pyridine DMHISM2 Discovery agent N.A. Investigative [21]
3-[4-Fluoro-indan-(1Z)-ylidenemethyl]-pyridine DMPS340 Discovery agent N.A. Investigative [22]
4'-(1-(pyridin-4-yl)propyl)biphenyl-3-ol DMEW1CP Discovery agent N.A. Investigative [20]
4'-(2-methyl-1-(pyridin-4-yl)propyl)biphenyl-3-ol DM6DSNI Discovery agent N.A. Investigative [20]
4'-(Pyridin-4-ylmethyl)biphenyl-3,4-diamine DMZ0H5X Discovery agent N.A. Investigative [21]
4'-(Pyridin-4-ylmethyl)biphenyl-3,4-diol DM6Z5EK Discovery agent N.A. Investigative [21]
4'-(Pyridin-4-ylmethyl)biphenyl-3-amine DMR8O1B Discovery agent N.A. Investigative [21]
4'-(Pyridin-4-ylmethyl)biphenyl-4-amine DM8HXYS Discovery agent N.A. Investigative [21]
4'-(Pyridin-4-ylmethyl)biphenyl-4-carboxamide DMYXMT6 Discovery agent N.A. Investigative [21]
4-((1H-imidazol-1-yl)methyl)benzonitrile DMFUBRC Discovery agent N.A. Investigative [10]
4-((1H-imidazol-1-yl)methyl)phenol DMYDGH4 Discovery agent N.A. Investigative [12]
4-((3',4'-Difluorobiphenyl-4-yl)methyl)pyridine DMHN5OL Discovery agent N.A. Investigative [21]
4-(4'-Fluoro-biphenyl-4-ylmethyl)pyridine DM52NMU Discovery agent N.A. Investigative [21]
4-(4-(thiophen-2-yl)benzyl)pyridine DMVXJU6 Discovery agent N.A. Investigative [21]
4-(4-(thiophen-3-yl)benzyl)pyridine DM7I21V Discovery agent N.A. Investigative [21]
4-Bromo-1-imidazol-1-ylmethyl-xanthen-9-one DMMVASI Discovery agent N.A. Investigative [14]
4-Indan-(1Z)-ylidenemethyl-pyridine DM25DR7 Discovery agent N.A. Investigative [22]
4-[(3'-Hydroxybiphenyl-4-yl)methyl]pyridine DM04MK7 Discovery agent N.A. Investigative [21]
4-[(4'-Hydroxybiphenyl-4-yl)methyl]pyridine DMIEMWA Discovery agent N.A. Investigative [21]
4-[1-(4'-Methoxybiphenyl-4-yl)propyl]pyridine DMCEABJ Discovery agent N.A. Investigative [21]
4-[4-(6-methoxynaphthalen-2-yl)benzyl]pyridine DM62351 Discovery agent N.A. Investigative [21]
4-[5-Bromo-indan-(1E)-ylidenemethyl]-pyridine DMI7YAQ Discovery agent N.A. Investigative [22]
4-[5-Bromo-indan-(1Z)-ylidenemethyl]-pyridine DMQKHXN Discovery agent N.A. Investigative [22]
4-[5-Chloro-indan-(1E)-ylidenemethyl]-pyridine DMZL8KN Discovery agent N.A. Investigative [22]
4-[5-Chloro-indan-(1Z)-ylidenemethyl]-pyridine DM1Z3DG Discovery agent N.A. Investigative [22]
4-[5-Fluoro-indan-(1E)-ylidenemethyl]-pyridine DMY08FE Discovery agent N.A. Investigative [22]
4-[5-Fluoro-indan-(1Z)-ylidenemethyl]-pyridine DMHDZUO Discovery agent N.A. Investigative [22]
5-[4-(Pyridin-4-ylmethyl)phenyl]-1H-indole DMW8RLN Discovery agent N.A. Investigative [21]
5-[5-Fluoro-indan-(1E)-ylidenemethyl]-pyrimidine DM2RIHT Discovery agent N.A. Investigative [22]
6-(3-(pyridin-4-yl)phenyl)naphthalen-2-ol DMA8TWC Discovery agent N.A. Investigative [23]
6-(pyridin-3-yl)-2-naphthonitrile DMC3SJI Discovery agent N.A. Investigative [19]
6-Pyridin-3-yl-3,4-dihydroquinoline-2(1H)-thione DMHAS2B Discovery agent N.A. Investigative [19]
6-Pyridin-3-yl-naphthalen-2-ol DMGWNDB Discovery agent N.A. Investigative [17]
6-[4-(Pyridin-4-ylmethyl)phenyl]naphthalen-2-ol DM40LQ9 Discovery agent N.A. Investigative [21]
7-(1-(1H-imidazol-1-yl)ethyl)-9H-fluoren-2-ol DMRPFNU Discovery agent N.A. Investigative [8]
ANG-3407 DMVI93X Prostate cancer 2C82.0 Investigative [24]
ISOCONAZOLE DMMF1HX Discovery agent N.A. Investigative [25]
N-(4'-Isonicotinoylbiphenyl-3-yl)acetamide DM2N3TG Discovery agent N.A. Investigative [21]
N-3-(4-bromophenyl)propyl imidazole DMFRD09 Discovery agent N.A. Investigative [11]
Rac-4'-(1-Imidazol-1-yl-propyl)-biphenyl-3,4-diol DMTN7IU Discovery agent N.A. Investigative [26]
Rac-4'-(1-Imidazol-1-yl-propyl)-biphenyl-3,5-diol DMQYRAB Discovery agent N.A. Investigative [26]
Rac-4'-(1-Imidazol-1-yl-propyl)-biphenyl-3-ol DMH2CX5 Discovery agent N.A. Investigative [26]
Rac-4'-(1-Imidazol-1-yl-propyl)-biphenyl-4-ol DMUQ6FW Discovery agent N.A. Investigative [26]
VN/107-1 DMJRI6A Prostate cancer 2C82.0 Investigative [24]
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⏷ Show the Full List of 89 Investigative Drug(s)

Molecular Expression Atlas (MEA) of This DTT

Molecular Expression Atlas (MEA) Jump to Detail Molecular Expression Atlas of This DTT
Disease Name ICD 11 Studied Tissue p-value Fold-Change Z-score
Prostate cancer 2C82 Prostate 6.87E-01 0.07 0.21
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The Drug-Metabolizing Enzyme (DME) Role of This DTT

DTT DME Name Steroid 17-alpha-monooxygenase (CYP17A1) DME Info
Gene Name CYP17A1
2 Approved Drug(s) Metabolized by This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
Aminophenazone DMY2AH1 N. A. N. A. Phase 4 [27]
Dihydrotestosterone DM3S8XC Prostate hyperplasia GA90 Phase 4 [28]
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1 Discontinued Drug(s) Metabolized by This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
Dexniguldipine DMLZIT2 Solid tumour/cancer 2A00-2F9Z Discontinued in Phase 2 [29]
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1 Investigative Drug(s) Metabolized by This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS DM1G4S9 Discovery agent N.A. Investigative [30]
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References

1 2011 FDA drug approvals. Nat Rev Drug Discov. 2012 Feb 1;11(2):91-4.
2 CYP17A1 inhibitors in castration-resistant prostate cancer.Steroids.2015 Mar;95:80-7.
3 Orteronel (TAK-700), a novel non-steroidal 17,20-lyase inhibitor: effects on steroid synthesis in human and monkey adrenal cells and serum steroid levels in cynomolgus monkeys. J Steroid Biochem Mol Biol. 2012 Apr;129(3-5):115-28.
4 Clinical pipeline report, company report or official report of Tavanta Therapeutics
5 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
6 Recent progress in pharmaceutical therapies for castration-resistant prostate cancer. Int J Mol Sci. 2013 Jul 4;14(7):13958-78.
7 Clinical pipeline report, company report or official report of DisperSol Technologies.
8 Synthesis, biological evaluation, and molecular modeling studies of methylene imidazole substituted biaryls as inhibitors of human 17alpha-hydroxyl... Bioorg Med Chem. 2008 Aug 15;16(16):7715-27.
9 Synthesis, biological evaluation and molecular modelling studies of methyleneimidazole substituted biaryls as inhibitors of human 17alpha-hydroxyla... Bioorg Med Chem. 2008 Feb 15;16(4):1992-2010.
10 Synthesis and biochemical evaluation of a range of potent benzyl imidazole-based compounds as potential inhibitors of the enzyme complex 17alpha-hy... Bioorg Med Chem Lett. 2006 Aug 1;16(15):4011-5.
11 Synthesis, biochemical evaluation and rationalisation of the inhibitory activity of a range of 4-substituted phenyl alkyl imidazole-based inhibitor... Bioorg Med Chem Lett. 2006 Sep 15;16(18):4752-6.
12 Synthesis and biochemical evaluation of a range of (4-substituted phenyl)sulfonate derivatives of 4-hydroxybenzyl imidazole-based compounds as pote... Bioorg Med Chem Lett. 2010 Sep 1;20(17):5345-8.
13 New selective nonsteroidal aromatase inhibitors: synthesis and inhibitory activity of 2,3 or 5-(alpha-azolylbenzyl)-1H-indoles. Bioorg Med Chem Lett. 1999 Feb 8;9(3):333-6.
14 A new class of nonsteroidal aromatase inhibitors: design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17 alpha-hydroxylase/C17,20-lyase. J Med Chem. 2001 Mar 1;44(5):672-80.
15 Novel highly potent and selective nonsteroidal aromatase inhibitors: synthesis, biological evaluation and structure-activity relationships investigation. J Med Chem. 2010 Jul 22;53(14):5347-51.
16 Hydroxyperfluoroazobenzenes: novel inhibitors of enzymes of androgen biosynthesis. J Med Chem. 1990 Sep;33(9):2452-5.
17 Heteroaryl-substituted naphthalenes and structurally modified derivatives: selective inhibitors of CYP11B2 for the treatment of congestive heart fa... J Med Chem. 2005 Oct 20;48(21):6632-42.
18 Synthesis and evaluation of heteroaryl-substituted dihydronaphthalenes and indenes: potent and selective inhibitors of aldosterone synthase (CYP11B... J Med Chem. 2006 Apr 6;49(7):2222-31.
19 In vivo active aldosterone synthase inhibitors with improved selectivity: lead optimization providing a series of pyridine substituted 3,4-dihydro-... J Med Chem. 2008 Dec 25;51(24):8077-87.
20 Isopropylidene substitution increases activity and selectivity of biphenylmethylene 4-pyridine type CYP17 inhibitors. J Med Chem. 2010 Jul 8;53(13):5049-53.
21 Replacement of imidazolyl by pyridyl in biphenylmethylenes results in selective CYP17 and dual CYP17/CYP11B1 inhibitors for the treatment of prosta... J Med Chem. 2010 Aug 12;53(15):5749-58.
22 Synthesis and evaluation of (pyridylmethylene)tetrahydronaphthalenes/-indanes and structurally modified derivatives: potent and selective inhibitor... J Med Chem. 2005 Mar 10;48(5):1563-75.
23 Synthesis, biological evaluation and molecular modelling studies of novel ACD- and ABD-ring steroidomimetics as inhibitors of CYP17. Bioorg Med Chem Lett. 2008 Jan 1;18(1):267-73.
24 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 1361).
25 Three dimensional pharmacophore modeling of human CYP17 inhibitors. Potential agents for prostate cancer therapy. J Med Chem. 2003 Jun 5;46(12):2345-51.
26 Novel CYP17 inhibitors: synthesis, biological evaluation, structure-activity relationships and modelling of methoxy- and hydroxy-substituted methyl... Eur J Med Chem. 2009 Jul;44(7):2765-75.
27 Contribution of human hepatic cytochrome P450s and steroidogenic CYP17 to the N-demethylation of aminopyrine. Xenobiotica. 1999 Feb;29(2):187-93.
28 Identifying susceptibility genes for prostate cancer--a family-based association study of polymorphisms in CYP17, CYP19, CYP11A1, and LH-beta. Cancer Epidemiol Biomarkers Prev. 2005 Aug;14(8):2035-9.
29 In vitro metabolism of dexamethasone (DEX) in human liver and kidney: the involvement of CYP3A4 and CYP17 (17,20 LYASE) and molecular modelling studies. Biochem Pharmacol. 1997 Sep 1;54(5):605-11.
30 Transcriptional complexes at the CYP17 CRS. Endocr Res. 2002 Nov;28(4):551-8.