NCT-506 is an orally bioavailable aldehyde dehydrogenase 1A1 (ALDH1A1) inhibitors with an IC50 of 7 nM. 了解更多

Ac-CoA Synthase Inhibitor1 is an anti-virus agent. 了解更多

Terphenyllin is a naturally abundant p-terphenyl metabolite isolated from the coral derived fungus Aspergillus candidus, has signi?cant α-glucosidase inhibitory activity. 了解更多

STING agonist-4 is an stimulator of Interferon Genes (STING) receptor agonist with an apparent inhibitory constant (IC50) of 20 nM. 了解更多

Propofol is a hypnotic alkylphenol derivative. Propofol is a General Anesthetic. Propofol is a short-acting medication that results in a decreased level of consciousness and lack of memory for events. Formulated for intravenous induction of sedation and hypnosis during anesthesia, propofol facilitates inhibitory neurotransmission mediated by gamma-aminobutyric acid (GABA). 了解更多

Proglumide is a drug that exerts an inhibitory effect on gastric secretion and reduces gastrointestinal motility. IProglumide is a known cholecystokinin (CCK) antagonist. 了解更多

Leukemia Inhibitory Factor Human Recombinant, HEK 了解更多

Leukemia Inhibitory Factor Receptor Alpha Human Recombinant 了解更多

Leukemia Inhibitory Factor Rat Recombinant 了解更多

Leukemia Inhibitory Factor Mouse Recombinant 了解更多

Leukemia Inhibitory Factor Human Recombinant 了解更多

Leukemia Inhibitory Factor Human Recombinant, Sf9 了解更多

Leukemia Inhibitory Factor, GST tag Human Recombinant 了解更多

Vascular Endothelial Growth InhibitorHuman Recombinant, His Tag 了解更多

Melanoma Inhibitory Activity Protein Human Recombinant, His Tag 了解更多

Melanoma Inhibitory Activity 2 Human Recombinant 了解更多

Melanoma Inhibitory Activity Human Recombinant 了解更多

Macrophage Migration Inhibitory Factor Mouse Recombinant 了解更多

Macrophage Migration Inhibitory Factor Human Recombinant (Active) 了解更多

Macrophage Migration Inhibitory Factor Human Recombinant 了解更多

Macrophage Migration Inhibitory Factor Human Recombinant, His Tag C-Terminus 了解更多

Macrophage Migration Inhibitory Factor Human, Recombinant His Tag N-Terminus 了解更多

Macrophage Migration Inhibitory Factor Rat Recombinant 了解更多

Macrophage Migration Inhibitory Factor, Mouse Anti Human 了解更多

WNT Inhibitory Factor 1 Human Recombinant 了解更多

WNT Inhibitory Factor 1 Mouse Recombinant 了解更多

Fas Apoptotic Inhibitory Molecule Human Recombinant 了解更多

ATPase Inhibitory Factor 1 Human Recombinant 了解更多

MAP3K12 Binding Inhibitory Protein 1 Human Recombinant 了解更多

Gastric Inhibitory Polypeptide Human Recombinant 了解更多

Calcineurin Autoinhibitory Peptide是Ca2+钙调蛋白依赖性蛋白磷酸酶（钙调神经磷酸酶）（IC50?10 uM）的选择性抑制剂。不抑制PP1，PP2A或CaM激酶II（IC50> 100 mM）。 了解更多

MIF Antagonist是MIF体外（IC50 = 7 μM）和细胞（IC50 = 25 μM）的多巴色素互变异构酶活性的抑制剂。 了解更多

Auranofin is a gold salt classified by the World Health Organization as an antirheumatic agent. It is a gold-thiol complex with anti-inflammatory and immunosuppressive actions. 了解更多

Cinnamylamine can be used for the preparation of Tranylcypromine, a drug that acts as a nonselective and irreversible inhibitor of the enzyme monoamine oxidase (MAO), and is used as an antidepressant and anxiolytic agent. 了解更多

ASN03576800 is an inhibitor of the VP40 matrix protein. 了解更多

Soporidine is a strigolactone (SL) antagonist and inhibitor of germination in their biological assays. It binds AtHTL and specifically interferes with SL signaling. 了解更多

BDTX-189 is a potent, orally active and selective inhibitor of allosteric EGFR and HER2 oncogenic mutations, including EGFR/HER2 exon 20 insertion mutants. BDTX-189 shows KDs of 0.2, 0.76, 13 and 1.2 nM for EGFR, HER2, BLK and RIPK2, reapectively. Anticancer activity. 了解更多

HS-1793 is a resveratrol analogue. HS-1793 downregulates the expression of hypoxia-induced HIF-1 and VEGF and inhibits tumor growth of human breast cancer cells in a nude mouse xenograft model. 了解更多

UCB-9260, an orally active compound, inhibits TNF signaling by stabilising an asymmetric form of the trimer. UCB-9260 is selective for TNF over other superfamily members, and binds TNF with a similar Kd of 13?nM. 了解更多

Ganoderic acid A can inhibit of the JAK-STAT3 signaling pathway, also inhibit proliferation, viability, ROS. 了解更多

CFI-400437 is a potent and selective inhibitor of polo-like kinase 4 (PLK4). 了解更多

XL092 is an ATP-competitive inhibitor of multiple RTKs including MET, VEGFR2, AXL and MER, with IC50 values in cell-based assays of 15, 1.6, 3.4, and 7.2 nM respectively. 了解更多

Topovale, also known as ARC-111, is a potent topoisomerase I inhibitor. 了解更多

WM 3835 is a lysine acetyltransferase HBO1 (KAT7) inhibitor. 了解更多

Etalocib, also known as LY293111 and VML295, is a potent and selective inhibitor of the lipoxygenase pathway either directly through 5'-lipoxygenase or via antagonism of the leukotriene B4 (LTB4) receptor. 了解更多

Pibrentasvir, also known as ABT-530, is a protease inhibitor potentially for the treatment of HCV infection. 了解更多

Sisunatovir, also known as RV521, is a highly potent fusion inhibitor with efficacy against a panel of clinical isolates of RSV-A and RSV-B viruses. 了解更多

AH10639 is a novel inhibitor of Pneumocystis carinii and Toxoplasma gondii dihydrofolate reductase. 了解更多

Merafloxacin, also known as CI 934, is a fluoroquinolone antibacterial, which was also identified as a ?1 PRF inhibitor of SARS-CoV-2. Frameshift inhibition by merafloxacin is robust to mutations within the pseudoknot region and is similarly effective on ?1 PRF of other beta coronaviruses. Importantly, frameshift inhibition by merafloxacin substantially impedes SARS-CoV-2 replication in Vero E6 cells, thereby providing the proof of principle of targeting ?1 PRF as an effective antiviral strategy for SARS-CoV-2. 了解更多