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Cat. No. Product Name Field of Application Chemical Structure
DCC2284 Gne-3476
Novel GluN2A-selective NMDA receptor positive allosteric modulator (PAM)
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DCC2283 Gne-203
Novel Met inhibitor
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DCC2282 Gne-0946
Novel potent and selective RORc inverse agonist
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DCC2281 Gne-0723
Novel GluN2A subunit-selective and brain-penetrant positive allosteric modulator (PAM) of The N-methyl-d-aspartate receptor (NMDAR)
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DCC2280 Gn39482
Novel Tubulin Polymerization Inhibitor
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DCC2279 Gmb-905
Negative control for GMB-805
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DCC2278 Gmb-805
Novel potent BCR-Abl PROTAC, inducing degradation and demonstrating in vivo activity
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DCC2277 Gma-839
Selective modulator of gamma-aminobutyric acid(A) receptors
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DCC2276 Gm3 N-12
Novel GM3 derivative, showing excellent migration and invasion inhibitory effects in cells and marked antitumor activity in C57BL/6 mice, involving focal adhesion and ECM-receptor interaction signaling pathways
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DCC2275 Glycitin 6"-o-malonate
Metabolite of soy isoflavones, promoting the proliferation of bone marrow stromal cells and osteoblasts and suppresses bone turnover
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DCC2274 Glut-in-30
Novel glucose transporter (GLUT) inhibitor, exhibited high antitumor potency through the suppression of glucose uptake (IC 50 : 2.5 μM), while not cytotoxic to prostate and mammary epithelial cells
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DCC2273 Glut-i2-nh2
Glucose transporter inhibitor linker for insulin conjugate
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DCC2272 Glut-i2
Selective inhibitor of human glucose transporter subtype 1/4 (hGLUT1/4)
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DCC2271 Glut-i1
Selective inhibitor of human glucose transporter subtype 1/4 (hGLUT1/4)
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DCC2270 Glut4-activator-26b
Novel potent glucose transporter type 4 (GLUT4) translocation activator, showing a significant blood glucose lowering effect in the severe diabetic mice model
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DCC2269 Gls1 Inhibitor Ll202
Novel inhibitor of glutaminase 1 (GLS1) with high binding affinity (SPR, Kd = 24 nM; ITC, Kd = 37 nM), exhibiting a similar in vivo antitumor activity as CB839
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DCC2268 Glpg0259
The first-in-class, ATP-competitive inhibitor of MAPKAPK5
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DCC2267 Glp-2r Modulator I
Ago-allosteric modulator of human GLP-2R
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DCC2266 Glp-2 (1-33) Acetate
Enteroendocrine hormone, stimulating the growth of intestinal epithelium
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DCC2265 Glo1-in-9
Novel inhibitor of glyoxalase 1 (Glo1), increasing the cellular methylglyoxal levels in human cells and suppressing the osteoclast formation of mouse bone marrow-derived macrophages
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DCC2264 Glo1-in-60
Novel potent Glyoxalase 1 (GLO1) inhibitor, demonstrating to penetrate the blood-brain barrier, elevating levels of methylglyoxal in the brain, and reducing depression-like behavior in mice
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DCC2263 Glmu-in-5175178
Novel inhibitor of the acetyltransferase activity of Escherichia coli N-acetylglucosamine-1-phosphate-uridyltransferase/glucosamine-1-phosphate-acetyltransferase (GlmU).
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DCC2262 Glipentide
Second-generation sulfonylurea, promoting the accumulation of fructose 2,6-bisphosphate in hepatocytes
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DCC2261 Glft2-in-31
Novel Galactofuranosyltransferase 2 (GlfT2) inhibitor
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DCC2260 Glenvastatin
Novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor
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DCC2259 glaziovianin A
Novel inhibitor of the cell cycle progression in M-phase; Inhibotor of endosome maturation
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DCC2258 Gkm001
First-in-class liver-selective glucokinase activator for the treatment of type 2 diabetes
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DCC2257 Gka-71
Novel and potent glucokinase activator (GKA)
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DCC2256 Gka-22
Novel Allosteric Activator of Human Glucokinase in the Absence of Glucose
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DCC2255 Gk-667
Novel water solubile prodrug of ICRF-193, penetrating into NVCMs, reaching intracellular concentrations sufficient to induce cytoprotective effects against ANT toxicity
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