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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC2312 Gps488
Novel HIV replication blocker (EC 50 = 1.66 μM), being actively against a panel of HIV mutant strains displaying resistance to individual drugs used in antiretroviral therapy
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DCC2311 Gpr88-agonist-84
Novel potent GPR88 agonist (EC 50 = 59 nM)
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DCC2310 Gpr88 Agonist 53
Novel, potent, efficacious, and brain-penetrant GPR88 agonist (cAMP EC 50 = 14 nM)
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DCC2309 Gpr52-in-43
Highly potent and specific GPR52 antagonist
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DCC2308 Gpr52-agonist-1b
The first orally active GPR52 agonist
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DCC2307 Gpr52-agonist-17
Novel potent GPR52 agonist, dose-dependently suppressing methamphetamine-induced hyperlocomotion in mice
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DCC2306 Gpr120-agonist-6a
Novel potent GPR120 agonist, exhibiting significant glucose-lowering effect and high selectivity over GPR40
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DCC2305 Gpi-15427
Potent PARP inhibitor
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DCC2304 Gpbar1-agonist-10
Novel selective non-steroidal agonist of G-protein bile acid receptor 1 (GPBAR1, also known as TGR5 or M-BAR)
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DCC2303 Go-y030
Curcumin analog, exhibiting potent growth suppressive activity in human colorectal carcinoma cells
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DCC2302 Govaniadine
Natural potent inducer of apoptosis in MCF-7 cell lines
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DCC2301 Govadine
Antipsychotic and cognitive enhancer; Dopamine D1 and D2 receptor modulator
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DCC2300 Gossypolone
Natural inhibitor of Musashi family of RNA-binding proteins
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DCC2299 Gonadorelin Acetate
Agonist of the GnRH receptor, inducing the secretion of the gonadotropins follicle-stimulating hormone and luteinizing hormone from the pituitary gland and to increase sex hormone production by the gonads
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DCC2298 Go/ldha-in-7
Dual Glycolate Oxidase/Lactate Dehydrogenase A (GO/LDHA) Inhibitor for Primary Hyperoxaluria
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DCC2297 Gnmt Inducer K-117
Novel potent GNMT inducer, inhibiting Huh7 cell growth in vitro and xenograft in vivo
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DCC2296 Gnlpt-in-1
Novel inhibitor of Gram-negative lipoprotein trafficking
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DCC2295 Gnidimacrin
Natural highly potent HIV latency-reversing agent
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DCC2294 gnf-pf-3834
Dose dependent up-regulator of the level of E-cadherin in SW620 cells
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DCC2293 Gnf-pf-3600
Novel inhibitor of Plasmodium falciparum, killing both blood- and sexual-stage P. falciparum parasites
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DCC2292 Gnf-pf-3539
Novel Inhibitor of EGF-EGFR Interactions
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DCC2290 Gnf351
Novel potent aryl hydrocarbon receptor (AHR) antagonist with the capacity to inhibit both DRE-dependent and -independent activity
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DCC2289 Gne-783
Novel selective CHK1 inhibitor
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DCC2288 Gne-6901
Novel GluN2A-selective NMDA receptor positive allosteric modulator (PAM)
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DCC2287 Gne-6689
Negative control for GNE-2256
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DCC2286 Gne-618
Novel inhibitor of nicotinamide phosphoribosyl transferase (NAMPT)
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DCC2285 Gne-5729
Novel NMDAR PAM with both an improved pharmacokinetic profile and increased selectivity against AMPARs
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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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