PROCATEROL HCL

Procaterol HCl provides the same bronchodilatory effect with enhanced formulation stability. Side effects include tachycardia, dizziness, tremor, and mild hypokalemia.

SKU: 7ead86f57722 Category: Tag:

Product Description


Mechanism of Action

PROCATEROL HCL (ID 27243) demonstrates a high‑complexity biochemical interaction profile characterised by multilayer signalling integration, modular enzymatic pathway penetration, mitochondrial network modulation, ion‑flux recalibration, redox‑state equilibrium restructuring and transcription‑factor axis reprogramming. Its molecular geometry enables conformational docking to catalytic pockets, allosteric domains, transmembrane receptor helices and cytoskeletal scaffolds, creating broad regulatory influence across metabolic, structural and genomic systems.

At the signalling level, PROCATEROL HCL may modulate phosphorylation gradients, kinome cascade propagation (including MAPK, JNK, ERK, PI3K–AKT, and AMPK axes), G‑protein subunit turnover, calcium wave propagation, secondary messenger amplification and stress‑adaptation thresholds. Mitochondrially, the compound can alter electron‑transport‑chain efficiency, ATP–ADP cycling, mitochondrial ROS leakage, membrane potential polarity and respiratory‑complex activation ratios.

Advanced Research Value

PROCATEROL HCL is particularly suited for:

  • Cross‑pathway interference mapping and kinome interaction grids
  • Ultra‑high resolution receptor–ligand docking and conformational prediction
  • Organelle‑stress modelling (ER stress, mitochondrial folding stress, autophagic flux modulation)
  • Network‑level transcriptome rewiring using multi‑omics clustering
  • Precision cytoskeletal‑mechanics analysis including actin polymerisation and tubulin turnover
  • Apoptotic vs. survival‑pathway bias quantification
  • Advanced SAR, QSAR and machine‑learning molecular‑performance modelling

Risks, Toxicodynamics & Cellular Hazard Spectrum

At elevated exposure levels, PROCATEROL HCL may induce:

  • ROS surge and oxidative collapse
  • Mitochondrial hyperfragmentation or respiratory‑complex shutdown
  • Severe ion‑channel destabilisation
  • Cytoskeletal disassembly and membrane‑integrity breach
  • Aberrant transcription‑factor activation, inflammatory bursts (NF‑κB, STAT, IRF pathways)
  • High‑grade apoptosis, necroptosis or ferroptosis initiation
  • Epigenetic instability affecting methylation/acetylation balance

Datasheet


Molecular Formula

C16H22N2O3·HCl

Molecular Weight

326.82 g/mol

CAS Number

62929-91-3

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

procaterol hydrochloride; 62929-91-3; 4VD1BRT7T8; Pro-Air; Lontermin

IUPAC/Chemical Name

8-hydroxy-5-[(1S,2R)-1-hydroxy-2-(propan-2-ylamino)butyl]-1H-quinolin-2-one;hydrochloride

InChl Key

AEQDBKHAAWUCMT-KKJWGQAZSA-N

InChl Code

InChI=1S/C16H22N2O3.ClH/c1-4-12(17-9(2)3)16(21)11-5-7-13(19)15-10(11)6-8-14(20)18-15;/h5-9,12,16-17,19,21H,4H2,1-3H3,(H,18,20);1H/t12-,16+;/m1./s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/16219912;

3D Conformer.

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