CHEBI:9605 - tirofiban

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ChEBI Name tirofiban
ChEBI ID CHEBI:9605
Definition 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.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:40602
Supplier Information
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Roles Classification
Biological Role(s): platelet glycoprotein-IIb/IIIa receptor antagonist
Antagonist of platelet surface glycoprotein-IIb/IIIa which has a key role in hemostasis and thrombosis such as platelet adhesion and aggregation.
Application(s): fibrin modulating drug
A drug that affects the function of fibrin in blood coagulation.
platelet glycoprotein-IIb/IIIa receptor antagonist
Antagonist of platelet surface glycoprotein-IIb/IIIa which has a key role in hemostasis and thrombosis such as platelet adhesion and aggregation.
anticoagulant
An agent that prevents blood clotting.
Related Structures
tirofiban is a Structural Derivative of
sulfonic acid
Mass : 82.08008
Formula : H2O3S
29214
oxoacid
Definition : A compound which contains oxygen, at least one other element, and at least one hydrogen bound to oxygen, and which produces a conjugate base by loss of positive hydrogen ion(s) (hydrons).
L-tyrosine
Mass : 181.18858
Formula : C9H11NO3
17895
L-phenylalanine
Mass : 165.18918
Formula : C9H11NO2
17295
phenylalanine
Mass : 165.18918
Formula : C9H11NO2
28044
proteinogenic amino acid
Definition : Any of the 23 alpha-amino acids that are precursors to proteins, and are incorporated into proteins during translation. The group includes the 20 amino acids encoded by the nuclear genes of eukaryotes together with selenocysteine, pyrrolysine, and N-formylmethionine. Apart from glycine, which is non-chiral, all have L configuration.
tyrosine
Mass : 181.18858
Formula : C9H11NO3
18186
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