Novel stimulator of host immune defenses, Inducing the transcription of putative immune effectors in C. elegans

Novel stimulator of autophagy, inhibiting Mycobacterium tuberculosis survival in macrophages, and targeting Pik1

Novel non-peptidic RANTES antagonist

Potent agonist of S1P1 receptors

Specific and competitive H2 receptor antagonist

Prodrug of the novel nucleoside phosphonate HIV reverse transcriptase (RT) inhibitor GS-9148

Novel nucleoside phosphonate HIV reverse transcriptase (RT) inhibitor

Photosensitiser for the treatment of age-related macular degeneration

Novel P2X3 antagonist

Novel potent and selective CB2 probe (Ki for CB2: 0.8 nM and >12000 selectivity over CB1)

Novel potent RORγt inverse agonist

Novel RORγt agonist

Novel RORgammaT inhibitor

Novel potent and selective RORγt agonist, showing robust antitumor efficacy in syngeneic tumor models and improving the efficacy of anti‑PD‑1 in a murine lung cancer model

The first potent inverse agonist of retinoid-related orphan receptor (ROR) with dual selectivity for RORβ and RORγt

Allosteric modulator of dextromethorphan binding to high-affinity sigma receptors

Novel p38α kinase inhibitor; Antioxidant

Lipid modifying agent; Antihyperlipidemic and antiarteriosclerotic

Anti-cancer agent, acting through gastrin antagonism and H /K -ATPase inhibition, modulating apoptosis pathways, antidyslipidemic, antiadipogenic, gastroprotective, antifertility, and antileishmanial

Novel potent and selective ROCK inhibitor

Novel potent and selective ROCK inhibitor

Novel potent and selective ROCK inhibitor

Potent Rho--​kinase (ROCK) inhibitor

Novel potent ROCK inhibitor

Novel potent competitive inhibitor of Rho-associated coiled-coil-containing protein kinase 2 (ROCKII)

Platelet-activating factor (PAF-R) antagonist, selectively for intracellular PAF binding sites

Selective antagonist at the 5-HT1A receptor

Novel potent γ-secretase modulator (GSM) with high solubility, balanced lipophilicity, and showing no phototoxicity and PIK4CB side bing activity

Novel potent and selectve LPA1 antagonist, attenuating NHLF human lung fibroblast cell proliferation and contraction in vitro, reducing plasma histamine levels in mouse LPA-challenge model

Potent γ-secretase modulator (GSM)