Eptifibatide

cas: 188627-80-7 — see every product listed under this CAS number, including other names

Eptifibatide (CAS 188627-80-7) is a chemical reagent available from Chemat. Available pack sizes: on request, 10mg, 100mg, 25mg, 5mg, 50mg, 10mM (in 1ml dmso), 1mg. Offered by: Chemat Brand, GLPBio, Biosynth, Sigma-Aldrich.

brandChemat Brand
catalog numberULPE126001
cas188627-80-7
sizeon request
availability Do potwierdzenia przez Chemat|To be confirmed by Chemat
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Available pack sizes

brand size price
Chemat Brand on request price on request
GLPBio 10mg 704.69 Pln
GLPBio 100mg 1991.83 Pln
GLPBio 25mg 1022.97 Pln
GLPBio 5mg 592.36 Pln
GLPBio 50mg 1397.41 Pln
GLPBio 10mM (in 1ml dmso) 681.29 Pln
Biosynth 5mg price on request
Biosynth 1mg price on request
Sigma-Aldrich 4.63MG 6026.00 Pln

properties

purityNo data
categoryChemicals
delivery timeTo be confirmed by Chemat

Eptifibatide is a synthetic homodetic cyclic peptide comprising Nalpha-(3-sulfanylpropanoyl)homoarginyl, glycyl, aspartyl, tryptophyl, prolyl and cysteinamide residues connected in sequence and cyclised via a disulfide bond. Derived from a protein found in the venom of the southeastern pygmy rattlesnake, Sistrurus miliarus barbouri, eptifibatide is an anti-coagulant that inhibits platelet aggregation by selectively blocking the platelet glycoprotein IIb/IIIa receptor, so preventing the binding of fibrinogen, von Willebrand factor, and other adhesive ligands. It is used in the management of unstable angina and in patients undergoing coronary angioplasty and stenting procedures. It has a role as an anticoagulant and a platelet aggregation inhibitor. It is a homodetic cyclic peptide, an organic disulfide and a macrocycle.

Source: ChEBI

Identity
Molecular formulaC35H49N11O9S2
Molecular weight832.0 g/mol
IUPAC name2-[(3S,6S,12S,20R,23S)-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]hexacosan-6-yl]acetic acid
InChIKeyCZKPOZZJODAYPZ-LROMGURASA-N
SMILESC1C[C@H]2C(=O)N[C@@H](CSSCCC(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@H](C(=O)N2C1)CC3=CNC4=CC=CC=C43)CC(=O)O)CCCCN=C(N)N)C(=O)N

Computed by PubChem (NCBI)

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