Novel osteoclastogenesis inhibitor, preventing ovariectomy-induced osteoporosis in ddY mice

Novel selective inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2), blocking VEGF-stimulated endothelial cell proliferation and migration and reducing tumor vessel permeability

Novel prodrug of luciferin to mimic the transport and activation of valacyclovir, , being a robust and functional determinant of VACVase activity

Natural pseudo-aminosugar

Prodrug of ganciclovir for treatment of cytomegalovirus (CMV) infection in those with HIV/AIDS or following organ transplant

Orally acting antinociceptive muscarinic agonist

Selective 5-HT2C receptor full agonist

Specific inhibitor of tissue Kallikrein>kallikrein

Novel potent inhibitor of FGFR4 kinase activity

Novel Mycobacterium Tuberculosis VapC-Activating Stapled Peptide, successfully penetrated Mycobacterium smegmatis cell membranes and exerted bactericidal activity at a minimum inhibitory concentration that inhibited 50% of the isolates (MIC50) < 6.25 μM

Novel Long Residence Time Superior Inhibitor of the Vasopressin V2 Receptor

Non-immunosuppressive immunophilins ligand, demonstrating enhanced neuroregeneration in the peripheral nervous system and CNS

Quorum sensing modulator as a LasR antagonist

Novel

Novel kidney urea transporter UT-A1 inhibitor

Novel USP30 inhibitor, increasing Ub-TOM20 with an EC50 of 2.45 mM and inducing the maximal Ub-TOM20

Novel H2 receptor agonist, functionally stimulating human cardiac H2 receptors in vitro and in vivo

Novel fluorescent histamine H3 receptor ligand

Novel NPY Y1 Receptor Antagonist

Novel H2 receptor agonist, functionally stimulating human cardiac H2 receptors in vitro and in vivo

Novel H2 receptor agonist, functionally stimulating human cardiac H2 receptors in vitro and in vivo

Novel subtype selective histamine H2 receptor G protein-biased agonist

Py-5-Labeled Fluorescent Multipurpose Probe for Investigations on the Histamine H3 and H4 Receptors, acting as a partial agonist at the hH3R [pEC50 (reporter gene) 8.77] and as an inverse agonist/antagonist at the h/mH4Rs [pIC50 (reporter gene) 8.76/7.08;

Novel potent partial agonist of histamine H4 receptors (H4R)

Novel potent partial agonist of histamine H4 receptors (H4R)

Potent, selective, and irreversible inhibitor of fatty acid amide hydrolase (FAAH)

Novel FAAH inhibitor

Novel Red-Emitting Fluorescent Dualsteric Probe for the Muscarinic Acetylcholine M2 Receptor

Natural flavonoid from the leaves of Glycyrrhiza uralensis

Novel Potent Neuropeptide Y Y4 Receptor (Y4R) Partial Agonist (pK i : 8.47)