3-Pyridyl Substituted Aliphatic Cycles as CYP11B2 Inhibitors: Aromaticity Abolishment of the Core Significantly Increased Selectivity over CYP1A2
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
3-Pyridyl Substituted Aliphatic Cycles as CYP11B2 Inhibitors: Aromaticity Abolishment of the Core Significantly Increased Selectivity over CYP1A2
Authors
Keywords
Electrospray ionization mass spectrometry, Oils, Chromatographic techniques, Aldosterone, Enzyme inhibitors, Ketones, Sodium carbonates, Hydrogen bonding
Journal
PLoS One
Volume 7, Issue 11, Pages e48048
Publisher
Public Library of Science (PLoS)
Online
2012-11-02
DOI
10.1371/journal.pone.0048048
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Novel Imidazol-1-ylmethyl Substituted 1,2,5,6-Tetrahydropyrrolo[3,2,1-ij]quinolin-4-ones as Potent and Selective CYP11B1 Inhibitors for the Treatment of Cushing’s Syndrome
- (2012) Lina Yin et al. JOURNAL OF MEDICINAL CHEMISTRY
- Selective Dual Inhibitors of CYP19 and CYP11B2: Targeting Cardiovascular Diseases Hiding in the Shadow of Breast Cancer
- (2012) Qingzhong Hu et al. JOURNAL OF MEDICINAL CHEMISTRY
- Synthesis and biological evaluation of imidazolylmethylacridones as cytochrome P-450 enzymes inhibitors
- (2012) Ashraf H. Abadi et al. MedChemComm
- Fine-Tuning the Selectivity of Aldosterone Synthase Inhibitors: Structure−Activity and Structure−Selectivity Insights from Studies of Heteroaryl Substituted 1,2,5,6-Tetrahydropyrrolo[3,2,1-ij]quinolin-4-one Derivatives
- (2011) Simon Lucas et al. JOURNAL OF MEDICINAL CHEMISTRY
- Design and synthesis of 1,3,5-trisubstituted 1,2,4-triazoles as CYP enzyme inhibitors
- (2011) Yaseen A. Al-Soud et al. TETRAHEDRON LETTERS
- Optimization of the First Selective Steroid-11β-hydroxylase (CYP11B1) Inhibitors for the Treatment of Cortisol Dependent Diseases
- (2011) Ulrike E. Hille et al. ACS Medicinal Chemistry Letters
- The Role of Fluorine Substitution in Biphenyl Methylene Imidazole-Type CYP17 Inhibitors for the Treatment of Prostate Carcinoma
- (2010) Qingzhong Hu et al. ChemMedChem
- Isopropylidene Substitution Increases Activity and Selectivity of Biphenylmethylene 4-Pyridine Type CYP17 Inhibitors
- (2010) Qingzhong Hu et al. JOURNAL OF MEDICINAL CHEMISTRY
- Replacement of Imidazolyl by Pyridyl in Biphenylmethylenes Results in Selective CYP17 and Dual CYP17/CYP11B1 Inhibitors for the Treatment of Prostate Cancer
- (2010) Qingzhong Hu et al. JOURNAL OF MEDICINAL CHEMISTRY
- Synthesis, Biological Evaluation, and Molecular Modeling of 1-Benzyl-1H-imidazoles as Selective Inhibitors of Aldosterone Synthase (CYP11B2)
- (2010) Luc Roumen et al. JOURNAL OF MEDICINAL CHEMISTRY
- First Selective CYP11B1 Inhibitors for the Treatment of Cortisol-Dependent Diseases
- (2010) Ulrike E. Hille et al. ACS Medicinal Chemistry Letters
- Steroidogenic cytochrome P450 (CYP) enzymes as drug targets: Combining substructures of known CYP inhibitors leads to compounds with different inhibitory profile
- (2009) Ulrike E. Hille et al. COMPTES RENDUS CHIMIE
- Novel CYP17 inhibitors: Synthesis, biological evaluation, structure–activity relationships and modelling of methoxy- and hydroxy-substituted methyleneimidazolyl biphenyls
- (2009) Ulrike E. Hille et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- CYP17 Inhibitors. Annulations of Additional Rings in Methylene Imidazole Substituted Biphenyls: Synthesis, Biological Evaluation and Molecular Modelling
- (2008) Mariano A. E. Pinto-Bazurco Mendieta et al. ARCHIV DER PHARMAZIE
- Synthesis, biological evaluation, and molecular modeling studies of methylene imidazole substituted biaryls as inhibitors of human 17α-hydroxylase-17,20-lyase (CYP17)—Part II: Core rigidification and influence of substituents at the methylene bridge
- (2008) Qingzhong Hu et al. BIOORGANIC & MEDICINAL CHEMISTRY
- Aldosterone synthase inhibition improves cardiovascular function and structure in rats with heart failure: a comparison with spironolactone
- (2008) P. Mulder et al. EUROPEAN HEART JOURNAL
- Synthesis, Biological Evaluation, and Molecular Modeling of Abiraterone Analogues: Novel CYP17 Inhibitors for the Treatment of Prostate Cancer
- (2008) Mariano A. E. Pinto-Bazurco Mendieta et al. JOURNAL OF MEDICINAL CHEMISTRY
- In Vivo Active Aldosterone Synthase Inhibitors with Improved Selectivity: Lead Optimization Providing a Series of Pyridine Substituted 3,4-Dihydro-1H-quinolin-2-one Derivatives
- (2008) Simon Lucas et al. JOURNAL OF MEDICINAL CHEMISTRY
- Overcoming Undesirable CYP1A2 Inhibition of Pyridylnaphthalene-Type Aldosterone Synthase Inhibitors: Influence of Heteroaryl Derivatization on Potency and Selectivity
- (2008) Ralf Heim et al. JOURNAL OF MEDICINAL CHEMISTRY
- Novel Aldosterone Synthase Inhibitors with Extended Carbocyclic Skeleton by a Combined Ligand-Based and Structure-Based Drug Design Approach
- (2008) Simon Lucas et al. JOURNAL OF MEDICINAL CHEMISTRY
- Synthesis, biological evaluation and molecular modelling studies of methyleneimidazole substituted biaryls as inhibitors of human 17α-hydroxylase-17,20-lyase (CYP17). Part I: Heterocyclic modifications of the core structure
- (2007) Carsten Jagusch et al. BIOORGANIC & MEDICINAL CHEMISTRY
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now