شماره ركورد كنفرانس :
3776
عنوان مقاله :
Efficient Approach for the Synthesis of Eptifibatide as Antiplatelet Drug
پديدآورندگان :
Hamdan Fatima K. N. Toosi University of Technology , Balalaie Saeed Balalaie@kntu.ac.ir K. N. Toosi University of Technology
تعداد صفحه :
1
كليدواژه :
,
سال انتشار :
1395
عنوان كنفرانس :
بيست چهارمين سمينار شيمي آلي ايران
زبان مدرك :
انگليسي
چكيده فارسي :
Over the years, peptides have been evolved as promising therapeutic agents in the treatment of cancer, diabetes, and cardiovascular diseases, and application of peptides in a variety of other therapeutic areas is growing rapidly. Eptifibatide is an antiplatelet drug of the glycoprotein IIb/IIIa inhibitor class (Figure 1). It is a cyclic heptapeptide which belongs to the class of the arginin-glycin-aspartat (RGD) mimetics and reversibly binds to platelets. Eptifibatide has a short half-life. The drug is the third inhibitor of GP IIb/IIIa that has found broad acceptance and has been approved by FDA in 1998 Herein, we wish to report the new approach for the synthesis of an API antiplatelet drug using Solid Phase Peptide Synthesis (SPPS) and suitable coupling reagents. The structure of compounds was confirmed based on the HR-MS (ESI) data. The details about synthetic approach and structure of product will be further discussed in the conference..
كشور :
ايران
لينک به اين مدرک :
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