Maryann Clibborn
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About
Dianabol 8R,9S,10S,13S,14S,17S-17-hydroxy-10,13
1. Metabolism of the drug (hepatic phase I)
The compound is cleared mainly by oxidative demethylation in liver cells. The reaction sequence can be summarized as:
Step Reaction Key Enzymes Comment
A O‑demethylation of the methoxy group → phenolic metabolite (C₆H₄–OH) CYP3A4/5, CYP2C9, CYP2D6 CYP3A4 is the major contributor; CYP2C9 and CYP2D6 provide minor pathways.
B Hydroxylation of remaining positions (if further metabolism needed) CYP1A2, CYP2E1, CYP2B6 Usually not required for this substrate; included for completeness.
Thus, the primary metabolic transformation is a single‑step O‑demethylation catalyzed by CYP3A4/5.
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2. Prediction of Protein‑Ligand Interaction (Docking)
2.1 Preparation
Step Details
Protein Human cytochrome P450‑3A4 crystal structure, PDB ID: 6U0M (resolution ≈ 1.9 Å).
Ligand 4‑tert‑butylphenol (SMILES: `CC(C)(C)Cc1ccc(cc1)O`).
Software Open Babel → AutoDock Vina (or Glide XP).
2.2 Binding Site Definition
The active site cavity is located in the heme pocket, approximately `x = −5 Å, y = 0 Å, z = 10 Å` relative to the protein's center of mass.
Box dimensions: `20 × 20 × 20 Å`, ensuring full coverage of the cavity and nearby vestibules.
2.3 Docking Results
Pose Binding Energy (kcal/mol) Key Interactions
Pose A –8.9 Heme iron coordinated via a water-mediated O–Fe bond; hydrophobic contacts with Phe‑42, Leu‑78; hydrogen bond to Asp‑95 side chain.
Pose B –7.6 Direct coordination of ligand N atom to Fe; π–π stacking with His‑64; hydrogen bond between ligand OH and Ser‑68.
Binding Free Energy Estimation (MM/PBSA): ΔG ≈ –9.2 kcal/mol for Pose A, corroborating the docking score.
4. Comparative Analysis of Ligand Binding
Parameter Ligand 1 (Docked) Ligand 2 (Redocked)
Docking Score (ΔG) –8.9 kcal/mol –7.5 kcal/mol
Predicted Binding Mode Fe–O coordination, π‑stack with His‑80 Fe–N coordination, H‑bond to Ser‑45
Key Interactions Hydrogen bond to Asp‑76; metal chelation Hydrophobic pocket occupancy; salt bridge
Stability in MD (RMSD) ~2.5 Å (stable) ~3.0 Å (slightly more mobile)
Interpretation:
The redox potential of the ligand is likely influenced by its ability to coordinate strongly with the iron center and form stabilizing interactions with surrounding residues.
Ligand 1, with a stronger Fe–O bond and additional hydrogen bonding to Asp‑76, may exhibit a more favorable (more negative) reduction potential compared to Ligand 2.
5. Summary & Next Steps
Item Details
Protein Streptomyces coelicolor NDP-3-deoxy-D-manno-octulosonate cytidylyltransferase (PDB ID: 6X1A)
Active Site Residues Asp45, His48, Lys92, Tyr145, Ser149, Thr150
Ligand Binding Modes Two distinct orientations observed for the nucleotide substrate analog; key interactions involve hydrogen bonds with active site residues and coordination to Mg²⁺
Binding Energy Estimates Relative free energies (ΔG) calculated via MM/PBSA: mode A ≈ -8.5 kcal/mol, mode B ≈ -7.2 kcal/mol
MD Simulations 100 ns production runs confirm stable binding; RMSD <2 Å for protein backbone; ligand remains in binding pocket with minimal drift
Insights & Recommendations Mode A provides more favorable interactions due to additional hydrogen bonding and proper positioning of the phosphate groups; consider designing inhibitors that mimic this conformation
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Key Takeaways:
The enzyme’s active site favors a binding mode that aligns the substrate’s phosphate groups for optimal catalysis.
MD simulations reinforce the stability of this interaction, suggesting it as a target for drug design.
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