Alternate TextTo enhance service speed and avoid tariff delays, we've opened a US warehouse. All US orders ship directly from our US facility.
Home > Products > Novel inhibitors

Novel inhibitors

You can also try the following methods, and our professionals will serve you Customized Consultation
Cat. No. Product Name Field of Application Chemical Structure
DCC2321 Gr-65630
5-HT3 receptor antagonist
More description
DCC2320 Gr-55562 Dihydrobromide
5-HT1B/5-HT1D serotonin receptor antagonist
More description
DCC2319 Gr269666a
Novel inhibitor of the EGFr and C-erbB-2.
More description
DCC2318 gr-205171 Dihydrochloride
Selective and brain penetrant NK1-receptor antagonist
More description
DCC2317 Gr134056x
Negative control for GI181771X
More description
DCC2316 Gr105659x
Potent TrkA kinase inhibitor
More description
DCC2315 G-quadruplex/i-motif Binder A9
Novel dual G-quadruplex/i-motif binder, binding to and stabilizing both G-quadruplex and i-motif, being effective in both oncogene replication and transcription
More description
DCC2314 Gqc-05
Novel high affinity, potent, and selective stabilizer of the MYC G-quadruplex (G4)., inducing cytotoxicity with corresponding decreased MYC mRNA and altering protein binding to the NHE III1 region
More description
DCC2313 Gpx4-in-26a
Novel potent and selective ferroptosis inducer, inhibiting glutathione peroxidase 4 (GPX4)
More description
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
More description
DCC2311 Gpr88-agonist-84
Novel potent GPR88 agonist (EC 50 = 59 nM)
More description
DCC2310 Gpr88 Agonist 53
Novel, potent, efficacious, and brain-penetrant GPR88 agonist (cAMP EC 50 = 14 nM)
More description
DCC2309 Gpr52-in-43
Highly potent and specific GPR52 antagonist
More description
DCC2308 Gpr52-agonist-1b
The first orally active GPR52 agonist
More description
DCC2307 Gpr52-agonist-17
Novel potent GPR52 agonist, dose-dependently suppressing methamphetamine-induced hyperlocomotion in mice
More description
DCC2306 Gpr120-agonist-6a
Novel potent GPR120 agonist, exhibiting significant glucose-lowering effect and high selectivity over GPR40
More description
DCC2305 Gpi-15427
Potent PARP inhibitor
More description
DCC2304 Gpbar1-agonist-10
Novel selective non-steroidal agonist of G-protein bile acid receptor 1 (GPBAR1, also known as TGR5 or M-BAR)
More description
DCC2303 Go-y030
Curcumin analog, exhibiting potent growth suppressive activity in human colorectal carcinoma cells
More description
DCC2302 Govaniadine
Natural potent inducer of apoptosis in MCF-7 cell lines
More description
DCC2301 Govadine
Antipsychotic and cognitive enhancer; Dopamine D1 and D2 receptor modulator
More description
DCC2300 Gossypolone
Natural inhibitor of Musashi family of RNA-binding proteins
More description
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
More description
DCC2298 Go/ldha-in-7
Dual Glycolate Oxidase/Lactate Dehydrogenase A (GO/LDHA) Inhibitor for Primary Hyperoxaluria
More description
DCC2297 Gnmt Inducer K-117
Novel potent GNMT inducer, inhibiting Huh7 cell growth in vitro and xenograft in vivo
More description
DCC2296 Gnlpt-in-1
Novel inhibitor of Gram-negative lipoprotein trafficking
More description
DCC2295 Gnidimacrin
Natural highly potent HIV latency-reversing agent
More description
DCC2294 gnf-pf-3834
Dose dependent up-regulator of the level of E-cadherin in SW620 cells
More description
DCC2293 Gnf-pf-3600
Novel inhibitor of Plasmodium falciparum, killing both blood- and sexual-stage P. falciparum parasites
More description
DCC2292 Gnf-pf-3539
Novel Inhibitor of EGF-EGFR Interactions
More description

Customized Consultation X

Your information is safe with us. * Required Fields.

Your name
Company
Email
Procuct Name
Cat. No.
Remark
Verification code
Please fill out the characters in the picture
X