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Tirofiban hydrochloride monohydrate

CAS No. 150915-40-5

Tirofiban hydrochloride monohydrate( L-700462 | MK-383 | MK-0383 )

Catalog No. M12110 CAS No. 150915-40-5

A potent, selective inhibitor of the platelet fibrinogen receptor GPIIb/IIIa with IC50 of 9 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 48 Get Quote
10MG 60 Get Quote
25MG 108 Get Quote
50MG 195 Get Quote
100MG 354 Get Quote
200MG 460 Get Quote
500MG Get Quote Get Quote
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Biological Information

  • Product Name
    Tirofiban hydrochloride monohydrate
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective inhibitor of the platelet fibrinogen receptor GPIIb/IIIa with IC50 of 9 nM.
  • Description
    A potent, selective inhibitor of the platelet fibrinogen receptor GPIIb/IIIa with IC50 of 9 nM, inhibition of platelet aggregation; displays > 24,000-fold over human umbilical vein endothelial cell fibrinogen receptors; inhibits ex vivo platelet aggregation induced by ADP in anesthetized dogs.Thrombosis Approved(In Vitro):Tirofiban hydrochloride monohydrate (0.25, 1, 3 μg/mL; 72 hours) increases proliferation of HAEC cells.Tirofiban hydrochloride monohydrate (24 hours) closes the scratch of HUVECs migration within 18 hours.Tirofiban hydrochloride monohydrate (0.25, 1 μg/mL; 1 hour) induces production of VEGF after 30 minutes which can stimulates proliferation of endothelial cells.(In Vivo):Tirofiban hydrochloride monohydrate (60 μg/kg; i.v.; once) shows activity of increasing contraction force, ventricular compliance, and improving heart function by increasing HR, LVESP, dp/dtmax, and reducing LVEDP.Tirofiban hydrochloride monohydrate (60 μg/kg; i.v.; once) enhances eNOS activity, decreases iNOS activity and reduces area of no-reflow after reperfusion following AMI. Tirofiban hydrochloride monohydrate (50 μg/per; irrigate; once) shows anticoagulant effect with patency rates of 59% at 24 hours after microvascular anastomosis in the crush model.
  • In Vitro
    Tirofiban hydrochloride monohydrate (0.25, 1, 3 μg/mL; 72 hours) increases proliferation of HAEC cells.Tirofiban hydrochloride monohydrate (24 hours) closes the scratch of HUVECs migration within 18 hours.Tirofiban hydrochloride monohydrate (0.25, 1 μg/mL; 1 hour) induces production of VEGF after 30 minutes which can stimulates proliferation of endothelial cells. Cell Proliferation Assay Cell Line:HAEC cells Concentration:0.25, 1, 3 μg/mL Incubation Time:72 hours Result:Increased proliferation of HAEC cells.Cell Migration Assay Cell Line:HUVEC cells Concentration:Incubation Time:24 hours Result:Stimulated the migratory capacity of endothelial cells.Western Blot Analysis Cell Line:HAEC cells Concentration:0.05, 0.12, 0.25, 1 μg/mL Incubation Time:1 hour Result:Induced production of VEGF which stimulated proliferation of endothelial cells.
  • In Vivo
    Tirofiban hydrochloride monohydrate (60 μg/kg; i.v.; once) shows activity of increasing contraction force, ventricular compliance, and improving heart function by increasing HR, LVESP, dp/dtmax, and reducing LVEDP.Tirofiban hydrochloride monohydrate (60 μg/kg; i.v.; once) enhances eNOS activity, decreases iNOS activity and reduces area of no-reflow after reperfusion following AMI.Tirofiban hydrochloride monohydrate (50 μg/per; irrigate; once) shows anticoagulant effect with patency rates of 59% at 24 hours after microvascular anastomosis in the crush model. Animal Model:Male Sprague-Dawley rats (10 to 15-week-age; 270-330 g).Dosage:60 μg/kg Administration:Intravenous injection; once.Result:Increased contraction force, ventricular compliance, and improved heart function.Reduced the size of no-reflow and infarct.Animal Model:Sprague-Dawley rats (350-400 g; crush injury model)Dosage:50 μg/per (50 μg/mL, 1 mL for each) Administration:Irrigate 1 mL within the vessel lumen (before placement of the last suture); once.Result:Showed anticoagulant effect with patency rates of 59%.
  • Synonyms
    L-700462 | MK-383 | MK-0383
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Integrin
  • Recptor
    GPIIb/IIIa
  • Research Area
    Cardiovascular Disease
  • Indication
    Thrombosis

Chemical Information

  • CAS Number
    150915-40-5
  • Formula Weight
    495.0728
  • Molecular Formula
    C22H39ClN2O6S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 12 mg/mL
  • SMILES
    CCCCS(=O)(=O)N[C@@H](CC1=CC=C(C=C1)OCCCCC2CCNCC2)C(=O)O.O.Cl
  • Chemical Name
    L-Tyrosine, N-(butylsulfonyl)-O-[4-(4-piperidinyl)butyl]-, hydrochloride, hydrate (1:1:1)

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Hartman GD, et al. J Med Chem. 1992 Nov 27;35(24):4640-2. 2. Lynch JJ Jr, et al. J Pharmacol Exp Ther. 1995 Jan;272(1):20-32. 3. Cook NS, et al. Thromb Haemost. 1993 Nov 15;70(5):838-47.
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