VALETHAMATE

Valethamate is an antispasmodic and anticholinergic used in obstetrics to relax cervical smooth muscle. Side effects include dry mouth, tachycardia, blurred vision, and dizziness.

SKU: 05d19949e6d2 Category: Tag:

Product Description


Mechanism of Action

VALETHAMATE (ID 27800) exhibits a high‑dimensional biochemical interaction matrix spanning signalling‑axis disruption, catalytic‑domain modulation, mitochondrial‑network recalibration, ion‑flux redistribution, cytoskeletal‑architecture remodelling, membrane‑potential rebalancing and transcription‑factor pathway restructuring. Its molecular topology supports interaction with catalytic residues, allosteric regulators, transmembrane helices, nucleotide‑binding pockets, redox‑buffer modules and polymeric scaffolding complexes, enabling wide‑band influence across metabolic, structural, genomic and electrophysiological domains.

Mechanistically, VALETHAMATE may reshape phosphorylation maps across ERK/MAPK/JNK/p38 axes, alter PI3K–AKT survival‑bias, modulate G‑protein coupling geometry, redistribute Ca²⁺ microdomain waveforms, adjust IP₃/DAG signalling topology and recalibrate cAMP–PKA amplitude. Mitochondrial impacts include ETC‑complex rebalancing, ATP/ADP cycle modulation, ROS‑threshold displacement, mitochondrial membrane‑potential polarity shifts and cross‑organelle stress signalling.

High‑Precision Research Applications

  • Kinome‑scale interference & catalytic‑cascade modelling
  • High‑resolution docking & conformational‑flow prediction
  • UPR/ER‑stress & autophagy/mitophagy integration networks
  • Full multi‑omics reconstruction (RNA‑seq, proteomics, phosphoproteomics, metabolomics)
  • Cytoskeletal force‑mapping & polymer turnover dynamics
  • Cell‑fate modelling: apoptosis, necroptosis, ferroptosis, parthanatos
  • AI‑driven SAR/QSAR predictive simulation

Toxicodynamics & Cellular Hazard Spectrum

  • Excessive ROS accumulation & antioxidant‑buffer collapse
  • Mitochondrial fragmentation or ETC suppression
  • Hyper‑disruption of Na⁺/K⁺/Ca²⁺ ionic‑gradients
  • Cytoskeletal degradation & membrane‑integrity failure
  • Inflammatory master‑switch activation (NF‑κB/STAT/IRF)
  • Multi‑axis programmed‑cell‑death induction
  • Epigenetic drift across methylation & acetylation layers

For expert laboratory research only — not intended for biological use.

Datasheet


Molecular Formula

C19H32NO2+

Molecular Weight

306.5 g/mol

CAS Number

16376-74-2

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

Valethamate; Valethamate ion; Valethamate cation; 16376-74-2; D64S64QVX7

IUPAC/Chemical Name

diethyl-methyl-[2-(3-methyl-2-phenylpentanoyl)oxyethyl]azanium

InChl Key

UPPMZCXMQRVMME-UHFFFAOYSA-N

InChl Code

InChI=1S/C19H32NO2/c1-6-16(4)18(17-12-10-9-11-13-17)19(21)22-15-14-20(5,7-2)8-3/h9-13,16,18H,6-8,14-15H2,1-5H3/q+1

References

https://pubchem.ncbi.nlm.nih.gov/compound/5648;

3D Conformer.

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