Unique antimigration and antiangiogenic agent

Closely related co-metabolite of cyclosporin A

Competitive nicotinic receptor antagonist

D1-like full agonist with similar affinity for D1 and D5, and roughly 10-fold selectivity over D2-like receptors

Novel dose-dependent inhibitor of the SARS-CoV-2 Mac1 Macrodomain

Corticosteroid Hormone Receptor Agonist

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Antiemetic agent used in the treatment of vomiting and vertigo

Muscle relaxant, causing general central nervous system depression, relieving pain caused by strains, sprains, and other musculoskeletal conditions

Novel inhibitor of CP4H activity in cultured cells at concentrations that do not cause iron deficiency

Novel inhibitor of CP4H activity in cultured cells at concentrations that do not cause iron deficiency

Inhibitor of DTDST inhibitor, a novel intestinal epigallocatechin gallate (EGCg) transporter

Natural Tat inhibitor, blocking HIV-1 transcription by specifically targeting the viral transactivator, Tat

Selective herbicide for the control of dicot weeds

Non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions

Major biliary metabolite of Diclofenac, a nonsteroidal antiinflammatory drug and COX inhibitor

Morin derivative, enhancing neural glyoxalase pathway (GP) activity and preventing methylglyoxal-mediated oxidative stress (OS) in an AD model

Histamine H1-receptor antagonist

Novel Inhibitor of the AAA-ATPase Drg1, blocking ribosome biogenesis

Selective alpha4beta2 nAChR partial agonist for the treatment of nicotine dependence to assist in smoking cessation

Novel probe for protein S-sulfinylation from cells

Novel potent and selective STING agonist, activating secretion of IFNβ, IL-6, TNF, and KC/GROα, exhibiting durable anti-tumour effects

Novel STING agonist with enhanced binding to STING and cellular function, displaying strong anti-tumour activity

Novel potent, selective and covalent inhibitor of DCN1, selectively inhibiting neddylation of cullin 3 in cells

The most potent inhibitor of sodium iodide symporter (NIS) reported to date

Novel Pim kinase inhibitor

Novel inducer of autophagic cell death through upregulation of HMGB1 in A549 cells

Novel growth inhibitor of both triple-positive and triple-negative human breast cancer cell lines

Novel HCV NS3 degrader, reducing susceptibility to resistance mutations, potently inhibiting HCV in a cellular infection model, exhibiting the most potent degradation (DC50 of 50nM at 4h) of HCV NS3,

Abundant lipid in the membranes of many algae, lower plants, and fungi, showing an inverse concentration relationship with phosphatidylcholine, being capable of replacing phosphatidylcholine