Identification Common Name Eptifibatide Class Small Molecule Description Eptifibatide is an organic compound with the chemical formula C35H49N11O9S2. Eptifibatide belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. With an average molecular weight of 831.97 g/mol, Eptifibatide is a heavy molecule.
This compound is found in or released from two recorded sources: antennas within electrical and electronic equipment, and antithrombotic agents within healthcare, pharmaceuticals, and veterinary products. The recorded route of exposure for this substance is intravenous. Eptifibatide acts upon five recorded protein targets, serving as an antagonist or modulator of Integrin beta-3 (ITGB3), Voltage-dependent calcium channel subunit alpha-2/delta-1 (CACNA2D1), Voltage-dependent N-type calcium channel subunit alpha-1B (CACNA1B), Voltage-dependent calcium channel subunit alpha-2/delta-2 (CACNA2D2), and one other protein.
Read more Contaminant Type Not Available Chemical Structure Synonyms Value Source N(6)-Amidino-N(2)-(3-mercaptopropionyl)-L-lysylglycyl-L-alpha-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide, cyclic(1-6)-disulfide ChEBI S(1),S(6)-Cyclo[N(6)-carbamimidoyl-N(2)-(3-sulfanylpropanoyl)-L-lysylglycyl-L-alpha-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide] ChEBI N(6)-Amidino-N(2)-(3-mercaptopropionyl)-L-lysylglycyl-L-a-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide, cyclic(1-6)-disulfide Generator N(6)-Amidino-N(2)-(3-mercaptopropionyl)-L-lysylglycyl-L-a-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide, cyclic(1-6)-disulphide Generator N(6)-Amidino-N(2)-(3-mercaptopropionyl)-L-lysylglycyl-L-alpha-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide, cyclic(1-6)-disulphide Generator N(6)-Amidino-N(2)-(3-mercaptopropionyl)-L-lysylglycyl-L-α-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide, cyclic(1-6)-disulfide Generator N(6)-Amidino-N(2)-(3-mercaptopropionyl)-L-lysylglycyl-L-α-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide, cyclic(1-6)-disulphide Generator S(1),S(6)-Cyclo[N(6)-carbamimidoyl-N(2)-(3-sulfanylpropanoyl)-L-lysylglycyl-L-a-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide] Generator S(1),S(6)-Cyclo[N(6)-carbamimidoyl-N(2)-(3-sulfanylpropanoyl)-L-lysylglycyl-L-α-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide] Generator S(1),S(6)-Cyclo[N(6)-carbamimidoyl-N(2)-(3-sulphanylpropanoyl)-L-lysylglycyl-L-a-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide] Generator S(1),S(6)-Cyclo[N(6)-carbamimidoyl-N(2)-(3-sulphanylpropanoyl)-L-lysylglycyl-L-alpha-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide] Generator S(1),S(6)-Cyclo[N(6)-carbamimidoyl-N(2)-(3-sulphanylpropanoyl)-L-lysylglycyl-L-α-aspartyl-L-tryptophyl-L-prolyl-L-cysteinamide] Generator Integrelin MeSH Integrilin MeSH Epifibatide MeSH Epifibratide MeSH
Read more Chemical Formula C35 H49 N11 O9 S2 Average Molecular Mass 831.970 g/mol Monoisotopic Mass 831.316 g/mol CAS Registry Number 188627-80-7 IUPAC Name 2-[(3R,11S,17S,20S,25aS)-11-(4-carbamimidamidobutyl)-1,9,12,15,18-pentahydroxy-3-(C-hydroxycarbonimidoyl)-20-[(1H-indol-3-yl)methyl]-21-oxo-3H,4H,7H,8H,11H,14H,17H,20H,21H,23H,24H,25H,25aH-pyrrolo[2,1-g]1,2-dithia-5,8,11,14,17,20-hexaazacyclotricosan-17-yl]acetic acid Traditional Name eptifibatide SMILES [H][C@@]12CCCN1C(=O)[C@]([H])(CC1=CNC3=CC=CC=C13)N=C(O)[C@]([H])(CC(O)=O)N=C(O)CN=C(O)[C@]([H])(CCCCNC(N)=N)N=C(O)CCSSC[C@]([H])(N=C2O)C(O)=N InChI Identifier InChI=1S/C35H49N11O9S2/c36-30(51)25-18-57-56-13-10-27(47)42-22(8-3-4-11-39-35(37)38)31(52)41-17-28(48)43-23(15-29(49)50)32(53)44-24(14-19-16-40-21-7-2-1-6-20(19)21)34(55)46-12-5-9-26(46)33(54)45-25/h1-2,6-7,16,22-26,40H,3-5,8-15,17-18H2,(H2,36,51)(H,41,52)(H,42,47)(H,43,48)(H,44,53)(H,45,54)(H,49,50)(H4,37,38,39)/t22-,23-,24-,25-,26-/m0/s1 InChI Key CZKPOZZJODAYPZ-LROMGURASA-N Chemical Taxonomy Description Belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Kingdom Organic compounds Super Class Organic acids and derivatives Class Carboxylic acids and derivatives Sub Class Amino acids, peptides, and analogues Direct Parent Glutamic acid and derivatives Alternative Parents Substituents Glutamic acid or derivatives
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
Hippuric acid
Hippuric acid or derivatives
Benzamide
Pyrrolo[2,3-d]pyrimidine
Benzoic acid or derivatives
Pyrrolopyrimidine
Benzoyl
Aminopyrimidine
Pyrimidone
Monocyclic benzene moiety
Pyrimidine
Substituted pyrrole
Benzenoid
Dicarboxylic acid or derivatives
Pyrrole
Vinylogous amide
Heteroaromatic compound
Amino acid
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid salt
Azacycle
Organic alkali metal salt
Carboxylic acid
Organoheterocyclic compound
Organic salt
Organic oxygen compound
Organic sodium salt
Organic nitrogen compound
Amine
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic zwitterion
Primary amine
Organonitrogen compound
Organooxygen compound
Aromatic heteropolycyclic compound Molecular Framework Aromatic heteropolycyclic compounds External Descriptors 
