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Tirofiban

CAS No.
144494-65-5
Chemical Name:
Tirofiban
Synonyms
Aggrastat;MK-383;C07965;CS-584;irofiban;TIROFIBAN;Tirofiban(L700462;Tirofiban USP/EP/BP;Tirofiban Impurity 10;Tirofiban/Tirofiban HCl
CBNumber:
CB9169083
Molecular Formula:
C22H36N2O5S
Molecular Weight:
440.6
MDL Number:
MFCD05237246
MOL File:
144494-65-5.mol
Last updated:2023-05-18 11:31:16

Tirofiban Properties

Melting point 223-225°
Boiling point 611.7±65.0 °C(Predicted)
Density 1.154±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Store in freezer, under -20°C
solubility Limited solubility
pka 3.37±0.10(Predicted)
BRN 6182267
CAS DataBase Reference 144494-65-5(CAS DataBase Reference)
FDA UNII GGX234SI5H
ATC code B01AC17

Pharmacokinetic data

Protein binding 65%
Excreted unchanged in urine 66%
Volume of distribution 22-42 Litres
Biological half-life 1.5-2 / Increased

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26
WGK Germany  3
RTECS  YP2364100

Tirofiban price More Price(20)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 30165 Tirofiban ≥98.5% (HPLC) 144494-65-5 5mg $235 2024-03-01 Buy
American Custom Chemicals Corporation API0005653 TIROFIBAN 95.00% 144494-65-5 5MG $503.93 2021-12-16 Buy
Adipogen Life Sciences CDX-T0153-M100 Tirofiban ≥99%(HPLC) 144494-65-5 100mg $1129 2021-12-16 Buy
AK Scientific E042 Tirofiban 144494-65-5 5mg $165 2021-12-16 Buy
American Custom Chemicals Corporation API0005653 TIROFIBAN 95.00% 144494-65-5 250MG $1248.45 2021-12-16 Buy
Product number Packaging Price Buy
30165 5mg $235 Buy
API0005653 5MG $503.93 Buy
CDX-T0153-M100 100mg $1129 Buy
E042 5mg $165 Buy
API0005653 250MG $1248.45 Buy

Tirofiban Chemical Properties,Uses,Production

Chemical Properties

Tirofiban is an Off-White to Pale Yellow Solid. It is soluble in organic solvents such as ethanol, DMSO, and dimethyl formamide, which should be purged with an inert gas. The solubility of tirofiban in these solvents is approximately 30 mg/ml.

Originator

Aggrastat,Merck and Co., Inc.

Uses

Tirofiban (Aggrastatt, MK-0383; L-700,462) is a parenteral, highly specific, and potent GPIIb/IIIa antagonist that was approved for patient use in 1998 for the treatment of unstable angina and non-Q-wave myocardial infarction.
Tirofiban is a nonpeptide GP IIb/IIIa antagonist that binds reversibly to IIb/IIIa receptors. Tirofiban is a non-peptide reversible antagonist of the platelet integrin glycoprotein (GP) IIbIIIa receptor used as an antiplatelet drug.
Tirofiban is a small molecule inhibitor of the protein-protein interaction between fibrinogen and the platelet integrin receptor GP IIb/IIIa and is the first drug candidate whose origins can be traced to a pharmacophore-based virtual screening lead.

Definition

ChEBI: Tirofiban is a member of the class of piperidines that is L-tyrosine in which a hydrogen attached to the amino group is replaced by a butylsulfonyl group and in which the hydrogen attached to the phenolic hydroxy group is replaced by a 4-(piperidin-4-yl)butyl group. It has a role as a fibrin modulating drug, a platelet glycoprotein-IIb/IIIa receptor antagonist and an anticoagulant. It is a member of piperidines, a sulfonamide and a L-tyrosine derivative.

Manufacturing Process

The synthesis of tirofiban starts by reaction of tyrosine with bis-trimethylsilyl trifluoraceramide to give a derivative in which both functions -OH and COOH_x0002_are protected. Treatment of this intermediate with butylsulfonyl chloride gives the corresponding sulfonamide derivative; the quite labile silyl groups are then removed under mildly acidic conditions to give N-butylsulfonyl-tyrosine. In a parallel scheme, 4-picoline is converted to its anion by means of butyl lithium; this gives 4-(4-chlorobutyl)-pyridine on alkylation with 1-bromo-3- chloropropane. The reaction of this compound with N-butylsulfonyl-tyrosine in presence of NaOH gives the ether 2-butylsulfonyaminol-3-[4-pyridin-4-ylbutoxy-phenyl]propionic acid. Hydrogenation over palladium on charcoal then reduce the pyridine ring to a piperidine to afford the fibrinogen receptor antagonist tirofiban.

Therapeutic Function

Fibrinogen receptor antagonist

General Description

Tirofiban is a nonpeptide that appears unrelatedchemically to eptifibatide, but actually has many similarities.The chemical architecture incorporates a systemthat is mimicking the RGD moiety that is present in eptifibatide.This can be seen in the distance between the nitrogenof the piperidine ring, which mimics the basic nitrogen ofarginine in the RGD sequence, and the carboxylic acid,which mimics the acid of aspartate in the RGD sequence.The basic nitrogen and the carboxylic acid of tirofiban areseparated by approximately 15 to 17? (16–18 atoms). Thisis the optimum distance seen in the RGD sequence of theplatelet receptor. Tirofiban is useful in treating non–Q wavemyocardial infarction and unstable angina.

Clinical Use

Tirofiban is a member of a new class of antithrombotic agents known as the “ fibans”. These compounds have a structural similarity to disintegrin, which was originally isolated from snake venoms. The location of the –COO- and NH3+ in the fibans is identical to the distance between the same functional groups of the RGD loop of disintegrin, and as a result, the fibans are able to effectively block the binding of fibrinogen to the GPIIb/IIIa receptor in an reversible manor.

Drug interactions

Potentially hazardous interactions with other drugs
Iloprost: increased risk of bleeding.
Heparin: increased risk of bleeding

Metabolism

Tirofiban is eliminated largely unchanged in the urine, with some biliary excretion in the faeces.

Mode of action

Tirofiban is a reversible antagonist that inhibits platelet aggregation by reversibly binding to the receptor glycoprotein (GP) IIb/IIIa of human platelets, thus preventing the binding of fibrinogen. Inhibition of platelet aggregation occurs in a dose- and concentrationdependent manner.?

149490-61-9
144494-65-5
Synthesis of Tirofiban from N-Butylsulfonyl-O-(4-(4-pyridinyl)butyl)-L-tyrosine
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View Lastest Price from Tirofiban manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Tirofiban pictures 2022-09-07 Tirofiban
144494-65-5
US $0.00-0.00 / kg 1kg 98% 250kg per month Shaanxi Dideu Medichem Co. Ltd
Tirofiban USP/EP/BP pictures 2021-08-07 Tirofiban USP/EP/BP
144494-65-5
US $1.10 / g 1g 99.9% 100 Tons min Dideu Industries Group Limited
Tirofiban pictures 2021-07-13 Tirofiban
144494-65-5
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
  • Tirofiban pictures
  • Tirofiban
    144494-65-5
  • US $0.00-0.00 / kg
  • 98%
  • Shaanxi Dideu Medichem Co. Ltd
  • Tirofiban pictures
  • Tirofiban
    144494-65-5
  • US $15.00-10.00 / KG
  • 99%+ HPLC
  • Zhuozhou Wenxi import and Export Co., Ltd

Tirofiban Spectrum

TIROFIBAN (2s)-2-(butylsulfonylamino)-3-[4-[4-(4-piperidyl)butoxy]phenyl]propanoic acid C07965 MK-383 N-(Butylsulfonyl)-O-[4-(4-piperidinyl)butyl]-L-tyrosine Tirofiban/Tirofiban HCl irofiban CS-584 AGGRASTAT; L700462; MK383 Tirofiban(L700462 (2S)-2-(butylsulfonylamino)-3-[4-(4-piperidin-4-ylbutoxy)phenyl]propanoicacid Tirofiban Impurity 10 Tirofiban USP/EP/BP Aggrastat Tirofiban (S)-2-(butylsulfonamido)-3-(4-(4-(piperidin-4- yl)butoxy)phenyl)propanoic acid 144494-65-5 144494-65-6 C22H30N2O5SD6 C22H36N2O5S Inhibitors