Potent inhibitor of tumor metastasis, inhibiting calmodulin, sialic acid, lipoperoxidation, fibrinogen, cell-movement and the cell-cycle arrest

Novel selective procaspase-8 (Pro-C8) Inhibitor covalently binding the zymogen, or inactive precursor (pro-form), of caspase-8, but not other caspases

Prodrug of NBDHEX, selectively inhibiting glutathione transferase (GST P1-1) with better water solubility, and more potent anticancer activities

Novel potent cereblon degrader with DC50 of 200 nM, and 64% protein degradation, as quantified by western blot

Novel highly potent degrader against EGFRL858R/T790M and EGFRdel19, reaching the lowest DC 50 values among all reported EGFR-targeting PROTACs

Novel SLC-targeting chimeric degrader, targeting SLC9A1 and other SLC9 family members, effectively impairing pH homeostasis and differentially killing cancer cell lines

Novel noncovalent CDK12/13 dual inhibitor, inducing potent and selective CDK12-CycK degradation without affecting CDK13, suppressing DDR-associated genes and induced synthetic lethality with Olaparib

Novel PI3K degrader, showing a significant and complete degradation effect on PI3K kinase at a concentration of 10 μM within 8 h

Novel potent and selective p38α and p38β degrader

Novel degrader of HMGCR protein, potently blocking cholesterol biosynthesis with less compensatory upregulation of HMGCR

Novel potent epidermal growth factor receptor (EGFR) degrader, inducing EGFRdel19 and EGFRL858R/T790M degradation with DC50 values of 0.51 and 126 nM, showing potent anti-proliferative activity against HCC827 and H1975 cell lines with IC50 values of 0.83

Novel potent degrader of H-PGDS protein via the ubiquitin-proteasome system and in the suppression of prostaglandin D2 (PGD2) production

Proteolysis targeting chimeras (PROTAC), providing broad tissue distribution and knockdown of the targeted ERRalpha protein in tumor xenografts

Proteolysis targeting chimeras (PROTAC), providing broad tissue distribution and knockdown of the targeted RIPK2 protein in tumor xenografts

Novel SirReal-based PROTAC, inducing isotype-selective Sirt2 degradation, resulting in the hyperacetylation of the microtubule network coupled with enhanced process elongation

Novel selective and potent Fak degrader

The most potent and selective ERRα degrader

Novel PROTAC, targeting steroid hormone receptors for ubiquitination and degradation

Novel bacterial polyyne contributing to the antioomycete and plant-protective effects of P. protegens

Novel selective CB2 agonist (CB2: 17.4 nM and CB1: 5585 nM)

Novel potent and selective inhibitor of SETD2

Selective 5-HT4 agonist

Novel selective 5-HT6 receptor antagonist, enhancing cognition and memory and potently decreasing food intake and body weight in rodents

Novel potent and selective 5-HT2B receptor antagonist

Novel inhibitor of upstream IκB kinase (IKK), specifically inhibiting the IκB phosphorylation and degradation and the subsequent nuclear translocation of NF-κB

Highly potent and selective VDR-coactivator inhibitor

Naturally occurring inhibitor of FOXO1a nuclear export

Unique inhibitor of bacterial chromosomal partitioning, increasing the efficacy of bortezomib and sorafenib through regulation of stress granule formation

Potent competitive antagonist and positive modulator of the P2X2 receptor with >100-fold selectivity versus P2X4, P2X7, and several investigated P2Y receptor subtypes (P2Y(2,4,6,12))

Positive modulator of ATP effects at P2X2 receptors

Potent competitive antagonist and positive modulator of the P2X2 receptor

Novel fluorescent-labeled selective adenosine A2B receptor antagonist

Highly potent, selective, competitive, and reversible inhibitor of monoamine oxidase B (MAO-B)

Highly potent, selective, competitive, and reversible inhibitor of monoamine oxidase B (MAO-B)

Highly potent, selective, competitive, and reversible inhibitor of monoamine oxidase B (MAO-B)

Novel potent Lp1NTPDase inhibitor

Novel Potent and Selective Antagonist for the UTP-Activated P2Y4 Receptor

Novel Potent Agonist of the Orphan G Protein-Coupled Receptor GPR17 (EC 50 12 nM)

Novel potent and selective agonist of the orphan G protein-coupled receptor 84 (GPR84)

Fluorescent Probe for Ecto-5'--nucleotidase (CD73)

Novel Potent Agonist of the Orphan G Protein-Coupled Receptor GPR17 (EC 50 27.9 nM)

Novel Potent Agonist of the Orphan G Protein-Coupled Receptor GPR17 (EC 50 32.1 nM)

Fluorescent Probe for Ecto-5'--nucleotidase (CD73)

The first potent and selective inhibitor of human nucleoside triphosphate diphosphohydrolase-2 (NTPDase2)

Novel Agonist of the Cannabinoid-Activated Orphan G-Protein-Coupled Receptor GPR18, being selective versus the CB-sensitive receptors CB1, CB2, and GPR55

Novel Agonist of the Cannabinoid-Activated Orphan G-Protein-Coupled Receptor GPR18, being selective versus the CB-sensitive receptors CB1, CB2, and GPR55

Potent GPR55 antagonist

Novel Selective, competitive GPR55 antagonist

Novel Highly Sensitive PSMA Probe for NIR-II Imaging and Intraoperative Tumor Resection, Visualizing Tumors in Real Time

Novel PSMA ligand conjugated with fluorescent dye SulfoCy7, demonstrating good visualization of PSMA-expressing tumors and the absence of any explicit toxicity up to 87.9 mg/kg

Na-K ATPase inhibitor, stimulating SERCA2a and accelerating calcium cycling in heart failure by relieving phospholamban inhibition

Novel Bovine Viral Diarrhea (BVD) Inhibitor, specifically blocking BVDV cell entry

Novel inhibitor of hypoxia-induced VEGF expression

Natural antifungal agent, against postharvest fruit pathogenic fungi

Novel CFTR modulator, increasing CFTR protein expression across different mutations, including F508del, by increasing CFTR mRNA levels by ~1.5 to ~2-fold in HBE cells

Novel CFTR modulator, binding to the poly-r(C) binding protein 1 (PCBP1), showing an affinity for RNA-bound PCBP1 higher than that of free PCBP1

Novel Brk/PTK6 kinase inhibitor

Novel Inhibitor of the PTK7/β-Catenin Interaction Targeting the Wnt Signaling Pathway in Colorectal Cancer

Novel Inhibitor of the PTK7/β-Catenin Interaction Targeting the Wnt Signaling Pathway in Colorectal Cancer

Novel Potent Multi-target PTK Inhibitor for the Treatment of Idiopathic Pulmonary Fibrosis (IPF)

Unique promoter of SMN2 exon 7 splicing, acting by directly stimulating splicing of exon 7

Novel NIR fluorescent probe for the detection of Aβ oligomers

Novel non-competitive potent and selective inhibitor of protein tyrosine phosphatase 1B (PTP1B)

Novel PTEN-like mitochondrial phosphatase PTPMT1 inhibitor

Novel thermally activated delayed fluorescence (TADF) molecule that exhibits high external quantum efficiency (EQE) in non-doped organic light-emitting diodes (OLEDs) at high luminescence

Hsp90α- and Hsp90ß-selective inhibitor

Novel specific inhibitor of tumor Hsp90

Hsp90α- and Hsp90ß-selective inhibitor

Novel specific Hsp90b1 inhibitor

Dual inhibitor of PDE3 and PDE4

Natural heat shock protein 90 (Hsp90) inhibitor, potentiating the echinocandin drug caspofungin in caspofungin-resistant fungal pathogens, blocking the induction of caspofungin-responding genes required for the adaptation to cell wall stress through the c

Novel Grp94-selective inhibitor PU-WS13 biotin probe

Novel potent and selective CHEK2>Chk2 inhibitor

Novel potent anticancer agent, disturbing microtubule formation at the centrosomes and inhibiting the growth of tumors dose-dependently in the HCT116 human colon cancer xenograft model in vivo

Novel Plasmodium vivax Hypoxanthine-Guanine Phosphoribosyltransferase Inhibitor

Novel selective FGF14:Nav1.6 PPI modulator

Inhibitor of cell death induced by oxidative stress and inhibitor of AB1-40 aggregation induced by Cu2+ ion

Novel potent inhibitor of collagen prolyl-4-hydroxylases (CP4H)

Novel suppressor of cancerous cell growth and proliferation

Bacterial siderophore, acting as an iron-chelating growth promoter for Pseudomonas aeruginosa

Novel inhibitor of p53-MDM2 interaction

Novel inhibitor of the PyrD protein (a dihydroorotate dehydrogenase (DHODase) involved in pyrimidine biosynthesis), suppressing bacterial cytotoxicity, biofilm formation and antibiotic resistance

Natural phytotoxin, inducing monopolar spindle formation and suppressing proliferation of cancer cells

Novel highly potent agonist of the apelin receptor (APJ) receptor (APJ cAMP EC50: human 0.023nM; rat 0.024nM; dog 0.030nM; monkey 0.080nM)

Novel KMD5A inhibitor

Novel BBB-permeable substrate of pyrilamine-sensitive proton-coupled organic cation antiporter (PYSOCA), acting as a selective class I HDAC inhibitor

Y2/Y5 Neuropeptide Y receptor agonist, reducing food intake in normal-weight and obese individuals and the plasma levels of the hunger-promoting hormone ghrelin

Novel inverse agonist of 5-HT6 receptor

Novel class of bright near infrared window II (NIR-II, 1,000 - 1,700 nm) probe, being successfully used to achieve high spatial and temporal resolution imaging of hind limb vasculature, lymphatic system, and small tumor metastasis, as well as precise NIR-

Selective PAR1 negative allosteric modulator

Novel Heme Oxygenase-1 Inhibitor (HO-1 IC 50 =0.27μM; HO-2 IC 50 =0.46μM)

Novel reactive oxygen species (ROS) inducer, showing significant cytotoxicity in pancreatic cancer cells

Novel Nav1.7 channel blocker (IC 50 at 3.5±1.5 μM). being efficacious on chronic pain in mice

Novel fluorescent molecular rotor for the selective detection of the hybrid-conformation 22AG G-Quadruplex

Novel potent inhibitor of quorum sensing (QS) pathways, strongly blocking agr-type QS in S. aureus

Novel potent inhibitor of quorum sensing (QS) pathways, strongly blocking agr-type QS in S. aureus

Novel multitarget anti-AD agent, significantly increasing in adult neurogenesis and remyelination through Prox1/NeuroD1 and Wnt/β-catenin pathways, demonstrating beneficial effects in preclinical models of AD

Novel photodynamic antitumor agent

Modulator of specific GABAA receptors via the benzodiazepine site on the GABAA receptor

Potent, orally active fungal Cyp51 (lanosterol 14-α-demethylase) inhibitor

Natural disrupter of DNA replication and transcription via DNA intercalation, reducing oxygen intake and carbohydrate metabolism and the excitability of muscle fibers, inhibiting the drug efflux pump P-glycoprotein

Novel antivirulence agent against Vibrio vulnificus, inhibiting the quorum-sensing signaling pathway by controlling the DNA-binding affinity of SmcR and thus effectively alleviating the virulence of V. vulnificus in vitro and in vivo

Novel microtubule destabilizer

Second-Generation GluN2C- and GluN2D-selective positive allosteric modulator (PAM) of the N-methyl-d-aspartate (NMDA) receptor

Novel Potent and Specific Ligand of r(CCUG)exp, Targeting r(CCUG) Repeats in Myotonic Dystrophy Type 2, Facilitating Degradation by RNA Quality Control Pathways

Novel scavenger receptor class B type I blocker

Novel inhibitor of HDL uptake induced by overexpression of scavenger receptor BI (SR-BI)

Novel Antiviral agent for Enterovirus D68

Efficient stabilizer of Mahoney procapsids

Potent and selective antagonist of 5-HT2A receptors

Novel inhibitor of PI3Kβ and PI3Kδ, inhibiting growth of PTEN deficient breast and prostate tumor

Prodrug of Racemetirosine, an inhibitor of tyrosine 3-monooxygenase

Novel potent DNA-alkylating agent, inhibiting TBP/DNA interaction

rac-NBI-74330 is a potent and selective CXCR3 antagonist.

Inhibitor of Janus kinases

Novel potent selective androgen receptor modulator (SARM)

Potent anti-free radical agent, elevating glutathione peroxidase (GSH-PX) and super oxide dismutase (SOD) levels and lowering malonaldehyde (MDA) level in vivo in the Alzheimer's model

Hsp90 N-terminal inhibitor

Novel inhibitor of the tyrosine kinase BCR-ABL and platelet-derived growth factor receptor, inhibiting mitosis entry in acute myeloid leukemia cells via suppression of Aurora kinase A expression

Novel potent inhibitor of p38 MAPK

Novel inhibitor of geranylgeranyl diphosphate synthase (GGDPS), showing significant reduction in tumor growth in mice

Novel inhibitor of geranylgeranyl diphosphate synthase (GGDPS)

Novel metabotropic glutamate type 5 (mGlu5) receptor negative allosteric modulator (NAM)

Potent fluorescent α4β1/α9β1 inhibitor

Novel dual inhibitor of dihydroceramide desaturase (dhCerDS) and acid ceramidase (ACDase)

Novel dual inhibitor of dihydroceramide desaturase (dhCerDS) and acid ceramidase (ACDase)

Selective inhibitor of poly(ADP-Ribose) glycohydrolase (PARG)

Novel highly potent, selective, and metabolically stable σ1 receptor agonist potentiating NGF-induced neurite outgrowth

Novel Potent Broad-Spectrum Inhibitor of Influenza A Virus RNA-Dependent RNA Polymerase (RdRp)

Novel HIV-1 Integrase Inhibitor

Novel HIV-1 Integrase Inhibitor

Novel potent inhibitor of RECQL5-helicase activity, and stabilizing RECQL5-RAD51 physical interaction, leading to impaired HRR and preferential killing of RECQL5-expressing breast cancer

Novel Prenyltransferase Inhibitor with In Vitro and In Vivo Antibacterial Activity

Novel potent inhibitor of the supercoiling and ATPase reactions of DNA gyrase, inhibiting gyrase by preventing the binding of ATP

Novel inhibitor of the supercoiling and ATPase reactions of DNA gyrase, inhibiting gyrase by preventing the binding of ATP and showing selectivity against M. smegmatis.

Novel specific inhibitor of the ability of RegA to activate its target promoters, reducing expression of a number of proteins required for virulence

Novel selective antagonist of the mGlu5 receptor

Potent ultra short-acting synthetic unique opioid analgesic

5-HT3 antagonist and 5-HT4 agonist, also acting as a 5-HT2B antagonist

Novel bacterial methionyl t-​RNA synthetase (MRS) inhibitor, hampering Plasmodium growth very effectively

Selective 5-HT1A receptor agonist

Oxidation-reduction indicator in cell viability

Potent VR1 vanilloid receptor agonist, activating protein kinase C

Angiotensin-converting enzyme 2 (ACE2) activator, acting as a modulator on RAAS and KKS activation during COVID-19

Red-absorbing, water-soluble, and iodinated resorufin derivative, being selectively activated with a monoamine oxidase (MAO) enzyme, showing high 1O 2 generation yields in aqueous solutions upon addition of MAO isoforms

Metabolite of Resveratrol

Metabolite of Resveratrol

Novel potent inhibitor of EBOV infection and entry

Novel inhibitor of the REV1/UbPCNA interaction, directly binding to REV1 UBM2 and preventing DNA damage tolerance (DDT)

Novel phosphodiesterase IV (PDE4) inhibitor for the treatment of Asthma and Rheumatoid Arthritis

Novel biomediator that induces reveromycins production at the wide range of concentrations without affecting cell growth

Novel TLR2 activator

Novel Highly Selective Neuropeptide FF1 Receptor Antagonist, Potently Preventing Opioid-Induced Hyperalgesia

Novel fluorescent D-amino acid for labeling peptidoglycans (PG) in live bacteria

Gene switch ligand as a transcription inducer for use in induceable gene expression systems

Highly Potent Clickable Probe for Cellular Imaging of MDM2 and Assessing Dynamic Responses to MDM2-p53 Inhibition

Potent, selective & ATP-competitive inhibitor of Cdks

Novel avß6 selective arginyl-glycinyl-aspartic acid (RGD)-mimetic, demonstrating to bind with extremely high affinity and selectivity for the alphavß6 integrin and having the potential as a clinical tool and therapeutic for investigating the role of avß6

Novel peptide-drug conjugate, inducing significant tumor growth suppression with negligible toxicity

Orally active, selective dopamine D3 receptor partial agonist

Novel Potent and Stable Antagonist of the Human α9α10 Nicotinic Acetylcholine Receptor for the Treatment of Neuropathic Pain

Potent inhibitor of Kv1.5 potassium channel

Novel inhibitor of the human papillomavirus (HPV) E6 oncoprotein

Novel Insect growth regulator, as potential insecticide to control olive fruit fly (Bactrocera oleae Rossi)

Potent tubulin assembly and cancer cell growth inhibitor

Quorum sensing modulator as a RhlR agonist

Novel potent and selective RhlR antagonist, strongly inhibiting biofilm formation, and reducing production of virulence factors in P. aeruginosa

Quorum sensing modulator as a RhlR antagonist

Selective sigma-2 ligand, inducing apoptosis in EMT-6 breast cancer cells

Potent inhibitor of the Rho pathway

Selective antagonist of the serotonin 5-HT3 receptor

Antibiotic for tuberculosis (TB) treatment

Natural antibiotic, inhibiting prokaryotic DNA-dependent RNA synthesis and protein synthesis; blocking RNA-polymerase transcription initiation, modulating ß2m aggregation

Water-soluble benzodiazepine prodrug, as a sedative and hypnotic neuropsychiatric agent

HIV-1 reverse transcriptase inhibitor, also acting as an EC 2.7.7.49 (RNA-directed DNA polymerase) inhibitor

Novel antidiabetic agent, impairing glucose uptake by muscle tissue, excessing hepatic gluconeogenesis, and increasing beta-cell apoptosis

Natural inducer of apoptosis by significantly upregulating Bcl-2, mitigating expression of Bcl2 in HCT 15 cells and attenuating the apoptotic markers and cell cycle regulatory proteins

First-in-Class Receptor Interacting Protein 2 (RIP2) Kinase Specific inhibitor

Novel IAP-based selective RIPK2 degrader

Novel peroxisome proliferator-activated receptor gamma (PPARgamma) agonist

Highly selective α4β2 subtype nicotinic receptor agonist

Novel potent Liver Receptor Homolog-1 (LRH-1) modulator

Novel inhibitor of dengue virus NS5 RNA-dependent RNA polymerase (RdRp), inhibiting the DENV type 2 (DENV2) RdRp activities

Natural selective inhibitor of protein tyrosine phosphatases (PTPases)

Novel potent and selective SIRT2 inhibitor, increasing the acetylation level of eukaryotic translation initiation factor 5A (eIF5A) and reducing cell viability of human breast cancer cells accompanied with a decrease in c-Myc expression

Novel selective inhibitor of activated fibroblasts, inhibiting the enhanced migration of fibroblasts cocultured with cancer cells by binding to β-arrestin1 and interfering with β-arrestin1-mediated cofilin signaling pathways

Novel potent and highly selective GPR6 inverse agonist, inhibiting GPR6 cAMP signalling in TR-FRET assays with a EC50 = 16 nM and >100 fold selectivity against GPR3 and GPR12

Novel gastrocolokinetic ghrelin agonist, approximately sixfold greater potency than natural ghrelin

Promising pro-apoptotic agent, showing activity on various cancer cell lines

Novel MOR agonist

Novel Fluorescent ER-Tracker dye, showing potent cytotoxic activity on several types of cancer cells, being accumulated into the endoplasmic reticulum (ER) as highlighted by its colocalization

The first irreversible covalent MPS1 inhibitor, targeting a poorly conserved cysteine in the kinase's hinge region

Potent, reversible, non-carbonyl inhibitor of fatty acid amide hydrolase (FAAH)

Novel potent and specific RNA-binding ligand, targeting riboswitches and other RNAs at proximal subsites

Selective antagonist of NMDA receptors NR2B subunits

Selective alpha1A/1L-adrenoceptor partial agonist

Potent and selective antagonist of NMDA glutamate receptors containing the NR2B subunit

Potent protein kinase C (PKC) inhibitor

ADAM17-selective inhibitor

Competitive AMPA receptor antagonist