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

Novel human α-galactosidase A ligand, capable of stabilizing α-Gal A and restoring trafficking

The major adduct formed by the food-borne carcinogen, PhIP with DNA

Selective inhibitor of diacylglycerol acyltransferase 2 (DGAT2)

Novel potent, orally active inhibitor of LTA4H

Proteolysis targeting chimeras (PROTAC), potently decreasing FKBP12 abundance in MV4;11 cells, leading to over 80% reduction of FKBP12 at 0.1 μM and 50% reduction at 0.01 μM

Cell-permeable, reversible and selective inhibitor of ɣ-secretase

Potent Squalene Synthase Inhibitor

5-HT3 Receptor antagonist; Antitussive; Anti-inflammatory; Antiasthmatic

Natural modulator of mu-, delta-, and kappa-opioid receptors

Norepinephrine-dopamine reuptake inhibitor (NDRI)

Cholecystokinin antagonist, selective for the CCKA subtype

Glucocorticoid, Anti-inflammatory Agent

Pro-drug of dexamethasone, anti-inflammatory glucocorticoid, stimulating glutamine uptake in the cerebral cortex

Cysteine reactive protein labeling agent

PET precursor of preparing radiolabel [11C]HD-800, a high affinity brain penetrant PET tracer for imaging microtubules

Primary metabolite of diazepam, binding to the GABA A receptor benzodiazepine modulatory site

Precursor for PET imaging 11C-radiolabeled MK-6884

Desfluoro impurity of Ezetimibe

Inhibitor of acetyl-CoA carboxylase (ACC), activating GPR40, inhibiting West Nile virus (WNV) infection and reducing the multiplication of Usutu virus (USUV), a WNV-related flavivirus

HIV-1 fusion inhibitor, targeting the membrane-proximal external region of Env spikes, specifically inhibiting the HIV-1 envelope-mediated membrane fusion by blocking CD4-induced conformational changes

Most efficient spin trap for the in vitro and in vivo detection of O-, N-, S- and C-centered free radicals

Selective anti-tumor agent, inducing apoptosis and inhibiting topoisomerase I

Novel selective and sensitive near-infrared fluorescent probe for visualization of endogenous nitric oxide in living cells and animals

Novel reversible microtubule inhibitor, increasing lysosomal V-ATPase activity and lysosome acidity