
188627-80-7
- Product Name:Eptifibatide
- Molecular Formula:C35H49N11O9S2
- Purity:99%
- Molecular Weight:831.974
Product Details;
CasNo: 188627-80-7
Molecular Formula: C35H49N11O9S2
Appearance: White powder
Quality products make an important contribution to long-term revenue and profitability. Manufacturer supply top purity Eptifibatide 188627-80-7 with ISO standards
1.What is the Eptifibatide ?
Eptifibatide is a platelet glycoprotein IIb/IIIa receptor reversible antagonist. It is used for acute coronary syndrome, coronary intervention before treatment and acute Q-wave myocardial infarction. It can relieve unstable angina symptoms and reduce the incidence of cardiovascular events.
Eptifibatide is a cyclical heptapeptide with anticoagulant activity. Eptifibatide selectively and reversibly binds to and blocks the platelet glycoprotein IIb/IIIa receptor. This prevents the binding of fibrinogen, von Willebrand factor, and other adhesive ligands and leads to an inhibition of platelet aggregation and prevents thrombus development. It is an efficient peptide drug to reduce the risk of cardiac ischemic events, however has a short half-life. Therefore, antithrombotic agents like eptifibatide are required to become improved with a protected and targeted delivery system such as using nano-liposomes to the site of thrombus.
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- 135900-78-6
Mpa-Har-Gly-Asp-Trp-Pro-Cys-NH2

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- 157630-07-4,188627-80-7
integrilin
Conditions | Yield |
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With ammonium hydroxide; In water; acetonitrile; at 23 ℃; for 2h; pH=9;
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63% |
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- 108-20-3
di-isopropyl ether

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- 6485-79-6
chlorotriisopropylsilane

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- 157630-07-4,188627-80-7
integrilin
Conditions | Yield |
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With trifluoroacetic acid; In dichloromethane; water; ethyl acetate;
|
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With trifluoroacetic acid; In dichloromethane; water; ethyl acetate;
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2.What is the CAS number for Eptifibatide ?
The CAS number of Eptifibatide is 188627-80-7.
More information of Eptifibatide 188627-80-7 are:
CAS Number |
188627-80-7 |
Density |
1.605 g/cm3 |
Refractive Index |
1.742 |
HS CODE |
2933299090 |
PSA |
374.49000 |
LogP |
1.62840 |
Pka |
4.01±0.10(Predicted) |
3.What are another words for Eptifibatide ?
Synonyms for Eptifibatide 188627-80-7:IntegratorsIntegrelin;L-Cysteinamide,N6-(aminoiminomethyl)-N2- (3-mercapto-1-oxopropyl)-L-lysylglycyl-L-Raspartyl- L-tryptophyl-L-prolyl-,cyclic (1f6)-disulfide;L-Cysteinamide, N6-(aminoiminomethyl)-N2-(3-mercapto-1-oxopropyl)-L-lysylglycyl-L-a-aspartyl-L-tryptophyl-L-prolyl-, cyclic (1?)-disulfide;2-[20-carbamoyl-12-[4-(diaminomethylideneamino)butyl]-3-(1H-indol-3-ylmethyl)-2,5,8,11,14,22-hexaoxo-17,18-dithia-1,4,7,10,13,21-hexazabicyclo[21.3.0]hexacos-6-yl]acetic acid;Integrilin;Integrelin;L-Cysteinamide, N6-(aminoiminomethyl)-N2-(3-mercapto-1-oxopropyl)-L-lysylglycyl-L-alpha-aspartyl-L-tryptophy-L-prolyl-, cyclic (1-6)-disulfide;
4.What is the molecular formula of Eptifibatide?
The chemical formula of Eptifibatide is C35H49N11O9S2 which containing 35 Carbon atoms,49 Hydrogen atoms,11 Nitrogen atoms,9 Oxygen atoms and 2 Sulfur atoms,and the molecular weight of Eptifibatide is 831.974.
5.What is Eptifibatide (188627-80-7) used for?
Eptifibatide is a reversible antagonist of the glycoprotein llb/llla complex, a specific platelet adhesion receptor that plays a central role in the cascade of thrombus formation by allowing mediators such as fibrinogen or von Willbrand factor to cross-link adjacent platelets and to give rise to aggregation. In diverse animal experimental models of arterial thrombosis, treatment with Eptifibatide resulted in an enhanced lysis of occlusive thrombus and a restoration of arterial blood flow. In clinical trials involving patients with acute coronary syndromes, Eptifibatide demonstrated a significant decrease in the incidence of death or nonfatal myocardial infarction at 30 days. In other trials in patients undergoing percutaneous coronary intervention (PCI), it showed a positive trend. Eptifibatide has the advantage of being short acting, its antiplatelet effect being rapidly reversible.
InChI:InChI=1/C35H49N11O9S2/c36-31(52)26-17-57-56-12-10-27(47)43-22(7-3-4-11-39-35(37)38)32(53)41-16-28(48)44-25(14-29(49)50)34(55)45-24(13-18-15-40-20-6-2-1-5-19(18)20)30(51)21-8-9-23(42-21)33(54)46-26/h1-2,5-6,15,21-26,40,42H,3-4,7-14,16-17H2,(H2,36,52)(H,41,53)(H,43,47)(H,44,48)(H,45,55)(H,46,54)(H,49,50)(H4,37,38,39)/t21?,22-,23-,24-,25-,26-/m0/s1
Relevant articles related to Eptifibatide:
Article |
Source |
Novel diphenylmethyl-derived amide protecting group for efficient liquid-phase peptide synthesis: AJIPHASE |
Takahashi, Daisuke,Yano, Tatsuya,Fukui, Tatsuya supporting information, p. 4514 - 4517 (2012/10/29) |
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