OXYPHENONIUM BROMIDE

Oxyphenonium bromide is an antimuscarinic agent decreasing GI motility and acid secretion. Side effects include tachycardia, dry mouth, and blurred vision.

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Product Description


Mechanism of Action

OXYPHENONIUM BROMIDE (ID 27003) 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, OXYPHENONIUM BROMIDE 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

C21H28BrNO3

Molecular Weight

428.4 g/mol

CAS Number

50-10-2

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

OXYPHENONIUM BROMIDE; 50-10-2; Spasmophen; Oxifenon; Oxyfenon

IUPAC/Chemical Name

2-(2-cyclohexyl-2-hydroxy-2-phenylacetyl)oxyethyl-diethyl-methylazanium bromide

InChl Key

UKLQXHUGTKWPSR-UHFFFAOYSA-M

InChl Code

InChI=1S/C21H34NO3.BrH/c1-4-22(3,5-2)16-17-25-20(23)21(24,18-12-8-6-9-13-18)19-14-10-7-11-15-19;/h6,8-9,12-13,19,24H,4-5,7,10-11,14-17H2,1-3H3;1H/q+1;/p-1

References

https://pubchem.ncbi.nlm.nih.gov/compound/5748;

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