Ak-HepaPur™ Dioleoyl Phosphatidylcholine (DOPC) is a phospholipid and is commonly used alone, or with other components, in the generation of micelles, liposomes and other types of artificial membranes.

Ak-HepaPur™ Polyenylphosphatidylcholines (PPC) is a phospholipid rich in polyunsaturated fatty acids. It is an important excipient and active ingredient for the preparation of liposomes and liver-targeted drug delivery systems.

Rapamycin is a potent and specific mTOR inhibitor.

Ertapenem sodium is a broad-spectrum long-acting β-lactam with activity against anaerobes.

α-Amanitin is the principal toxin of several deadly poisonous mushrooms, exerting its toxic function by inhibiting RNA-polymerase II.

Teduglutide is an analog of human glucagon-like peptide-2 (GLP-2).

Cefotaxime sodium is a β-lactamase stable third-generation cephalosporin.

Acipimox is a nicotinic acid analogue that inhibits lipolysis.

Semaglutide, a long-acting GLP-1 analogue, is a glucagon-like peptide-1 (GLP-1) receptor agonist.

Colchicine is a microtubule protein inhibitor. It binds to tubulin dimers, prevents microtubule formation, and thereby inhibits cell mitosis. It is also a competitive antagonist of the α3 glycine receptor.

Galanthamine hydrobromide is a selective, reversible, competitive, alkaloid AChE inhibitor.

Podofilox (Podophyllotoxin) is a potent inhibitor of microtubule assembly and DNA topoisomerase II.

1-Chloroethyl palmitate is a long-chain fatty acid ester featuring a C16 hydrophobic fatty chain and a chloroethyl reactive site; it can be used in the development of lipid derivatives and functionalized ester intermediates.

Triptolide is a diterpenoid triepoxide and acts as an NF-κB activation inhibitor.

Ursodeoxycholic acid is a secondary bile acid issued from the transformation of (cheno)deoxycholic acid by intestinal bacteria, acting through interactions with bile acid-activated receptors including TGR5 and FXR.

Eriodictyol is an active TRPV1 receptor antagonist.