OXOMEMAZINE HCL

Oxomemazine HCl provides identical antihistaminic and sedative effects in a more stable salt form. Side effects include dizziness, anticholinergic effects, and rare allergic reactions.

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Product Description


Mechanism of Action

OXOMEMAZINE HCL (ID 26993) exhibits a multidimensional biochemical activity profile involving modulation of enzyme-catalyzed pathways, receptor-mediated intracellular signaling, ion-channel regulation, mitochondrial bioenergetics, oxidative-stress balancing, membrane dynamics, and transcription-factor orchestration. Its molecular configuration allows high-affinity interaction with catalytic residues, allosteric domains, regulatory scaffolds, and signaling intermediates, influencing phosphorylation cycles, second‑messenger flux (Ca²⁺, cAMP, IP₃, DAG), ROS equilibrium, ATP synthesis, and mitochondrial respiratory-chain regulation.

Depending on dose, exposure duration, and cell type, OXOMEMAZINE HCL can modify chromatin accessibility, metabolic flux routing, vesicular trafficking, cytoskeletal structure, and gene-expression clusters associated with survival, inflammation, apoptosis, autophagy, and metabolic adaptation.

Benefits and Advantages

Due to its consistent mechanistic behavior, this compound is utilized in advanced research, including:

  • Receptor–ligand interaction studies and affinity modeling
  • High‑resolution enzyme kinetics and catalytic-pathway deconstruction
  • Mitochondrial ATP‑flux assays and oxidative‑stress system modeling
  • Multi‑omics profiling (transcriptomics, proteomics, metabolomics, phosphoproteomics)
  • Cytoskeletal and membrane‑dynamics exploration
  • Apoptosis, ferroptosis, necroptosis, and autophagy pathway analysis
  • Structure–activity relationship (SAR) investigations and compound optimization
  • Pharmacodynamic modeling, mechanistic dose–response scaling, and pathway benchmarking

Side Effects and Risks

Potential laboratory risks include:

  • Oxidative‑stress imbalance and ROS accumulation
  • Mitochondrial overload or respiratory-chain suppression
  • Ion‑channel dysregulation affecting Ca²⁺/Na⁺/K⁺ homeostasis
  • Unintended receptor cross‑activation or pathway inhibition
  • Cytoskeletal destabilization and membrane‑integrity disruption
  • Dose-dependent cytotoxicity (apoptotic or autophagic induction)
  • Transcriptional or epigenetic instability under prolonged exposure
  • Activation of inflammatory signaling networks (NF‑κB, JNK, p38 MAPK)

Use strictly in controlled laboratory environments with appropriate biosafety protocols.

Datasheet


Molecular Formula

C18H23ClN2O2S

Molecular Weight

366.9 g/mol

CAS Number

4784-40-1

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

Oxomemazine hydrochloride; 4784-40-1; EINECS 225-330-4; UNII-6BOK44G9K6; 6BOK44G9K6

IUPAC/Chemical Name

3-(5,5-dioxophenothiazin-10-yl)-N,N,2-trimethylpropan-1-amine;hydrochloride

InChl Key

NPMMOYKGIWLASW-UHFFFAOYSA-N

InChl Code

InChI=1S/C18H22N2O2S.ClH/c1-14(12-19(2)3)13-20-15-8-4-6-10-17(15)23(21,22)18-11-7-5-9-16(18)20;/h4-11,14H,12-13H2,1-3H3;1H

References

https://pubchem.ncbi.nlm.nih.gov/compound/3083870;

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