Target intelligence / Profile preview

Fibrin (Factor Ia)

Target
Factor Ia
Molecular classification
Protein, Extracellular matrix protein
01

Overview

Fibrin, also known as Factor Ia, is a fibrous, non-globular protein that plays a crucial role in blood clotting (hemostasis). It is formed through the conversion of fibrinogen, a soluble plasma protein, by the action of the protease enzyme thrombin. This conversion and subsequent polymerization of fibrin is essential for wound healing and preventing excessive blood loss. Fibrin is the major component of blood clots, forming a mesh atop platelet plugs at wound sites to prevent blood loss. It also provides a scaffold for cell migration and tissue repair during the wound healing process. Abnormalities in fibrin formation or degradation are associated with various pathological conditions, including thrombosis, hemorrhagic disorders, cancer, and cardiovascular disease. Fibrin degradation products (FDPs), particularly D-dimer, are measured to detect conditions involving abnormal clot formation or dissolution.

Other names
Factor IaFibrin clot
02

Mechanism of action

Modulating fibrinogen levels or targeting fibrin-dependent interactions

03

Biological functions

HemostasisWound healingInflammationAngiogenesisBlood clot formationTissue repair
04

Disease associations

ThrombosisHemorrhagic disordersCancerCardiovascular diseaseNeurological disordersDisseminated Intravascular Coagulation (DIC)AfibrinogenemiaHypofibrinogenemiaDysfibrinogenemiaHypodysfibrinogenemia
05

Safety considerations

Excessive generation of fibrin leading to thrombosisIneffective generation or premature breakdown of fibrin increasing the risk of hemorrhage
06

Interacting drugs

Heparin

1 more in the full profile.

07

Biomarkers

Fibrin degradation products (FDPs)D-dimer

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