TIROFIBAN

Tirofiban is a glycoprotein IIb/IIIa inhibitor preventing platelet aggregation, used in acute coronary syndromes. Side effects include bleeding, thrombocytopenia, hypotension, and injection‑site reactions requiring close monitoring.

SKU: 4a84c1b4f8a7 Category: Tag:

Product Description


Mechanism of Action

TIROFIBAN (ID 27686) exerts multi‑axis biochemical modulation involving enzymatic‑cascade interference, receptor‑mediated signalling adjustment, oxidative‑stress balancing, mitochondrial‑respiratory modulation, ion‑channel behaviour influence, cytoskeletal‑architecture modification and transcription‑factor regulatory alignment. Its molecular topology supports potential interaction with catalytic residues, allosteric microdomains, membrane‑anchored receptor systems and intracellular signalling scaffolds. These interactions affect phosphorylation circuits, Ca²⁺ signalling, IP₃/DAG turnover, cAMP regulation, ATP flux and cellular redox‑state stability.

Benefits & Applications

  • Receptor–ligand interaction and docking studies
  • Kinase/catalytic pathway profiling
  • Mitochondrial ATP/ROS functional modelling
  • Multi‑omics integration research
  • Cytoskeletal and membrane‑dynamics analysis
  • Apoptosis, autophagy and survival‑pathway investigations
  • SAR/QSAR modelling and molecular optimisation

Risks & Side Effects

  • ROS accumulation and oxidative‑stress imbalance
  • Mitochondrial overload or ETC suppression
  • Ion‑channel destabilisation (Ca²⁺/Na⁺/K⁺)
  • Cytoskeletal disruption and membrane integrity loss
  • Dose‑dependent cytotoxicity
  • Inflammatory cascade activation

Datasheet


Molecular Formula

C22H24N2O5S

Molecular Weight

440.6 g/mol

CAS Number

144494-65-5

Storage Condition

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

Solubility

Very slightly soluble

Purity

Purity information is available upon request (COA).

Synonym

tirofiban; 144494-65-5; Agrastat; tirofibanum; N-(Butylsulfonyl)-O-(4-(4-piperidyl)butyl)-L-tyrosine

IUPAC/Chemical Name

(2S)-2-(butylsulfonylamino)-3-[4-(4-piperidin-4-ylbutoxy)phenyl]propanoic acid

InChl Key

COKMIXFXJJXBQG-NRFANRHFSA-N

InChl Code

InChI=1S/C22H36N2O5S/c1-2-3-16-30(27,28)24-21(22(25)26)17-19-7-9-20(10-8-19)29-15-5-4-6-18-11-13-23-14-12-18/h7-10,18,21,23-24H,2-6,11-17H2,1H3,(H,25,26)/t21-/m0/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/60947;

3D Conformer.

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