Plays important role in regulation of blood pressure

Selective blocker of inward-rectifier K+ channels

α7 subtype-selective nAChR antagonist

Designed to capture high-mannose, hybrid, and complex type glycosylated peptides from complex protein mixtures

Potent C5a receptor antagonist

PKG inhibitor

Inhibitor of actin polymerization

PAR2 receptor agonist

High affinity MDM2 inhibitor

Mitochondria VDAC modulator; also Ferroptosis activator

Selective PAR4 antagonist

High affinity and selective allosteric KSP inhibitor

Deuterated olanzapine (Cat. No. 4349)

Potent K2P2.1 (TREK-1) channel blocker

High affinity, selective NPR3 antagonist

Wnt5a peptide mimetic

Highly potent and selective NOP agonist

Endogenous agonist for retinoic acid receptors; inducer of neuronal differentiation

Nrf2 signaling activator

Inhibitor of fibrinogen aggregation and fibrin polymerization

Shown to inhibit fibronectin function by binding to platelet-binding sites and to induce apoptosis in osteoblasts

Chemotactic peptide for polymorphonuclear leukocytes

Shown to inhibit fibronectin binding to platelet-binding sites

Acts as a functional antagonist of inflammatory mediators

Active in cell adhesion and cell-surface receptor binding and in stimulating cell migration

Inactive control peptide for other fibronectin inhibitors

Inhibitor of protein kinases G and A

Annexin/lipocortin 1-mimetic; inhibits leukocyte extravasation

Selective and potent c-MET kinase inhibitor

Deuterated fenretinide (Cat. No. 1396)