TADALAFIL

Tadalafil is a PDE5 inhibitor enhancing nitricoxidemediated vasodilation for erectile dysfunction and pulmonary hypertension. Side effects include headache, flushing, dyspepsia, back pain, nasal congestion, and rare priapism. Only GMP materials will be supplied, logistics all according to GDP.

SKU: b886c2da1ff1 Category: Tag:

Product Description


Mechanism of Action

TADALAFIL exhibits a highly distributed biochemical activity matrix spanning multiaxis signalling disruption, enzymaticcascade interference, mitochondrialnetwork recalibration, cytoskeletal remodelling, redoxsystem modulation, ionflux redistribution and transcriptionfactor pathway realignment. Its conformational topology enables interaction with catalytic cores, allosteric domains, transmembrane helices, hydrophobic receptor cavities, nucleotidebinding pockets and multiprotein scaffolding structures. This generates systemwide modulation across metabolic, genomic, structural and electrophysiological domains.

At the signalling level, TADALAFIL may reshape phosphorylation gradients, modify propagation dynamics across MAPK/ERK/JNK/p38 axes, alter PI3KAKT survival signalling, shift Gprotein coupling states, recalibrate intracellular Ca²⁺ microdomains, and modulate IP/DAG and cAMPPKA signalling amplitudes. Mitochondrial effects include ETCcomplex rebalancing, ATPturnover adjustment, ROSleakage threshold modulation and membranepotential polarity shifts. Its multinode regulation enables deep experimental interrogation of stressadaptation pathways and metabolicresponse thresholds.

HighResolution

  • Ultrascale kinome interference mapping & catalyticcascade simulation
  • Highfidelity receptorligand docking & conformationalflow modelling
  • Organelle crosstalk modelling (UPR, mitochondrial/ER stress, mitophagy dynamics)
  • Multiomics regulatorynetwork reconstruction (RNAseq, metabolomics, proteomics, phosphoproteomics)
  • Advanced cytoskeletal biomechanics (actin/tubulin turnover, tensionmapping)
  • Cellfate modelling across apoptosis, necroptosis, ferroptosis, parthanatos & autophagic flux axes
  • AIenhanced SAR/QSAR molecularperformance prediction

Toxicodynamics & Hazard Profile

  • Accelerated ROS accumulation & antioxidant-system saturation
  • Mitochondrial fragmentation or ETCchain destabilisation
  • Severe Ca²⁺/Na⁺/K⁺ ionic-flux dysregulation
  • Cytoskeletal depolymerisation & loss of mechanical integrity
  • Membrane damage, permeability shifts & lipidbilayer thinning
  • Inflammatory overactivation via NF-κB, STAT & IRF signalling
  • Multiple programmed-cell-death pathway activation
  • Epigenetic distortions (methylation drift, acetylation imbalance)

For expert laboratory research only not intended for biological exposure.

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

Datasheet


Molecular Formula

C22H19N3O4

Molecular Weight

389.4 g/mol

CAS Number

171596-29-5

Storage Condition

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

Solubility

Practically insoluble in water

Purity

Purity information is available upon request (COA).

Synonym

Tadalafil; Cialis; 171596-29-5; Ic351; ADCIRCA

IUPAC/Chemical Name

(2R,8R)-2-(1,3-benzodioxol-5-yl)-6-methyl-3,6,17-triazatetracyclo[8.7.0.03,8.011,16]heptadeca-1(10),11,13,15-tetraene-4,7-dione

InChl Key

WOXKDUGGOYFFRN-IIBYNOLFSA-N

InChl Code

InChI=1S/C22H19N3O4/c1-24-10-19(26)25-16(22(24)27)9-14-13-4-2-3-5-15(13)23-20(14)21(25)12-6-7-17-18(8-12)29-11-28-17/h2-8,16,21,23H,9-11H2,1H3/t16-,21-/m1/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/110635;

3D Conformer.

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