SULFAMETHOXYPYRIDAZINE (SMP)

Sulfamethoxypyridazine (SMP) is a sulfonamide inhibiting bacterial folate synthesis, used in veterinary and research contexts. Side effects include GI upset, hypersensitivity, and renal crystallization. Only GMP materials will be supplied, logistics all according to GDP.

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Product Description


Mechanism of Action

SULFAMETHOXYPYRIDAZINE (SMP) exhibits an expansive biochemical activity architecture integrating multidirectional signalling modulation, catalyticpathway interference, mitochondrialnetwork recalibration, ionflux reorganisation, cytoskeletal remodelling, membranedynamics alteration and transcriptionfactor axis redistribution. Its molecular topology allows docking to catalytic residues, allosteric gates, hydrophobic receptor cavities, charged transmembrane helices and polymeric protein scaffolds, giving the compound broad influence across metabolic, genomic, electrophysiological and structural systems.

At the signalling level, SULFAMETHOXYPYRIDAZINE (SMP) may perturb phosphorylation gradients, alter ERK/JNK/MAPK propagation velocities, reorganise PI3KAKT survivalpathway bias, shift Gprotein coupling efficiency, regulate Ca²⁺ microdomains, reshape IP/DAG secondarymessenger maps and influence cAMPPKA amplitude dynamics. Mitochondrially, it may modify membranepotential polarity, adjust ETC complex activation ratios, reshape ATP/ADP turnover behaviour and alter ROS leakage thresholds.

HighPrecision

  • Deep kinome interference mapping and signallingcascade simulations
  • Highresolution docking, ligandstability prediction & conformational flow analysis
  • Mitochondrial stress modelling & organelle crosstalk dynamics
  • UPR/ERstress and integrated autophagymitophagy pathway analysis
  • Multiomics regulatorynetwork reconstruction (transcriptome, phosphoproteome, metabolome)
  • Actin/tubulin turnover modelling and cytoskeletal forcedistribution mapping
  • Cellfate mapping across apoptosis, necroptosis, ferroptosis and parthanatos
  • Machinelearning SAR/QSAR pipelines for advanced molecular optimisation

Toxicodynamics & Cellular Hazard Spectrum

  • ROS surge and collapse of antioxidantbuffer systems
  • Mitochondrial fragmentation or ETCchain suppression
  • Severe ionic-flux destabilisation including Ca²⁺ overload
  • Cytoskeletal disassembly & membrane-integrity breakdown
  • Hyperactivation of NF-κB, STAT and IRF inflammatory axes
  • Induction of programmed-cell-death pathways
  • Epigenetic drift affecting methylation, acetylation and chromatin compaction

For expert not intended for biological exposure.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C11H12N4O3S

Molecular Weight

280.3 g/mol

CAS Number

80-35-3

Storage Condition

Store at 2-8°C

Solubility

Soluble in water

Purity

Purity information is available upon request (COA).

Synonym

sulfamethoxypyridazine; 80-35-3; Sulphamethoxypyridazine; Midicel; Sulfapyridazine

IUPAC/Chemical Name

4-amino-N-(3-methoxy-4-pyridyl)benzenesulfonamide

InChl Key

Unavailable

InChl Code

Unavailable

References

PubChem; ChemBL; FDA;

3D Conformer.

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