TRAZODONE HCL

Trazodone HCl is a serotonin antagonist and reuptake inhibitor used for depression and insomnia. Side effects include sedation, dizziness, priapism, orthostatic hypotension, and GI disturbances.

SKU: 4f9c7096f3b3 Category: Tag:

Product Description


Mechanism of Action

TRAZODONE HCL (ID 27726) demonstrates a multi‑layer biochemical interaction architecture integrating high‑bandwidth signalling interference, catalytic‑domain perturbation, mitochondrial‑network recalibration, ion‑flux redistribution, cytoskeletal restructuring, membrane‑potential modulation and transcription‑factor pathway realignment. Its molecular conformation enables docking to catalytic residues, allosteric nodes, transmembrane helices, nucleotide‑binding pockets, redox‑buffer centres and polymeric scaffolding complexes, providing system‑wide influence across metabolic, electrophysiological, structural and genomic domains.

At the signalling stratum, TRAZODONE HCL may reshape phosphorylation landscapes, alter the propagation kinetics of ERK, MAPK, JNK and p38 pathways, modulate PI3K–AKT survival gating, adjust G‑protein coupling efficiency, redistribute Ca²⁺ microdomains, influence IP₃/DAG signalling geometry, and redefine cAMP‑PKA amplitude. Mitochondrial effects include ETC‑complex rebalancing, ATP/ADP cycle remapping, ROS‑threshold displacement, membrane‑potential polarity modulation and cross‑organelle stress signalling.

High‑Precision Research Applications

  • Kinome‑scale cascade interference mapping & catalytic‑pathway reconstruction
  • High‑resolution docking, ligand‑meta‑stability tracking & conformational‑flow modelling
  • UPR/ER‑stress, mitophagy and organelle cross‑talk quantification
  • Multi‑omics regulatory‑network reconstruction (RNA‑seq, metabolomics, phosphoproteomics, proteomics)
  • Cytoskeletal mechanics including actin/tubulin turnover and force‑distribution modelling
  • Cell‑fate simulations across apoptosis, necroptosis, ferroptosis & parthanatos pathways
  • AI‑enhanced SAR/QSAR optimisation engines for predictive compound modelling

Toxicodynamics & Cellular Hazard Spectrum

  • Acute ROS surge and antioxidant‑buffer saturation
  • Mitochondrial fragmentation or ETC‑axis collapse
  • Severe Na⁺/K⁺/Ca²⁺ ion‑homeostasis destabilisation
  • Cytoskeletal depolymerisation & structural‑integrity failure
  • Membrane‑tension breakdown & lipid‑bilayer thinning
  • Hyperactivation of inflammatory master regulators (NF‑κB, STAT, IRF families)
  • Activation of multiple programmed‑cell‑death pathways
  • Epigenetic drift including methylation and acetylation instability

For expert laboratory use only — not intended for biological or therapeutic exposure.

Datasheet


Molecular Formula

C19H22ClN5O·HCl

Molecular Weight

408.3 g/mol

CAS Number

25332-39-2

Storage Condition

Store at 20 deg to 25 °C (68 deg to 77 °F).

Solubility

2.90e-01 g/L

Purity

Purity information is available upon request (COA).

Synonym

Trazodone hydrochloride; 25332-39-2; Trazodone Hcl; Trialodine; Oleptro

IUPAC/Chemical Name

2-[3-[4-(3-chlorophenyl)piperazin-1-yl]propyl]-[1,2,4]triazolo[4,3-a]pyridin-3-one;hydrochloride

InChl Key

OHHDIOKRWWOXMT-UHFFFAOYSA-N

InChl Code

InChI=1S/C19H22ClN5O.ClH/c20-16-5-3-6-17(15-16)23-13-11-22(12-14-23)8-4-10-25-19(26)24-9-2-1-7-18(24)21-25;/h1-3,5-7,9,15H,4,8,10-14H2;1H

References

https://pubchem.ncbi.nlm.nih.gov/compound/62935;

3D Conformer.

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