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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DC8514 AMG-1 Featured AMG-1 is a potent inhibitor of human c-Met and RON with IC50 values of 4 and 9 nmol/L respectively.
DC20661 AMG-1694 AMG1694 is a potent, small molecule Glucokinase (GK)-GKRP (GK regulatory protein) disruptor, does not block the GK binding site directly.
DC23850 AMG-458(AMG458;AMG 458) AMG-458 (AMG458) is a potent, selective, orally bioavailable c-Met inhibitor with Ki of 1.2 nM (human c-Met).
DC20664 AMG-548 Featured AMG-548 is a potent and selective inhibitor of p38α with Ki of 0.5 nM, dispalys weak inhibition for p38β (Ki=3.6 nM), and >5,000-fold selectivity over p38γ and p38δ; shows >1,000-fold selectivity over other 36 kinases, and is efficacious in acute and chro
DC12430 AMG7703 AMG7703 (4-CMTB, AMG-7703) is an allosteric, selective agonist of FFAR2 (GPR43)..
DC8503 AMG-Tie2-1 Featured AMG-Tie2-1 is a highly potent, non-selective inhibitor of Tie-2 (IC50 <1 nM).
DC9548 Amicarbazone Amicarbazone(BAY-MKH3586; BAY314666) is a potent inhibitor of photosynthetic electron transport via binding to the Qb domain of photosystem II (PSII); herbicide with a broad spectrum of weed control.
DCAPI1263 Amidopyrine Amidopyrine is white crystalline substance used as an analgesic and antipyretic.
DCAPI1043 Amikacin hydrate Amikacin is an aminoglycoside antibiotic used to treat different types of bacterial infections.
DC8984 Aminoglutethimide Aminoglutethimide is an aromatase inhibitor with IC50 of 10 μM.
DC11324 Aminopeptidase N Inhibitor Aminopeptidase N (AP-N) inhibitor is a reversible inhibitor of AP-N/CD13 (IC50 = 25 μM).
DC11193 Aminopyridine 2 Aminopyridine 2 (MPO inhibitor AP-2) is a novel potent, selective, orally available inhibitor of Myeloperoxidase (MPO), inhibits MPO peroxidase activity in vitro and in human plasma with IC50 of 0.16 and 1.9 uM, respectively.
DC20206 Amitriptyline;MK-230, N-750, Ro41575 Amitriptyline is a tricyclic antidepressant (TCA) with analgesic properties, widely used to treat depression and neuropathic pain.
DC9181 Amlodipine Besylate Amlodipine besylate is a long-acting calcium channel blocker.
DCAPI1067 Ammonium Glycyrrhizinate (AMGZ) Ammonium Glycyrrhizinate (AMGZ)
DC20178 Pyrrolidinedithiocarbamate ammonium;APDC, PDTC Featured Ammonium pyrrolidine dithiocarbamate (PDTC) is a potent nuclear factor-κB (NF-κB) inhibitor that inhibits IκB phosphorylation, blocks NF-κB translocation to the nucleus and reduces the expression of downstream cytokines.
DC20188 Amodiaquine Amodiaquine is a synthetic aminoquinoline that acts by binding to the protozoal or parasitic DNA and preventing DNA and RNA production and subsequent protein synthesis. It is used for the therapy of malaria.
DCAPI1343 Amorolfine HCl Featured Amorolfine hydrochloride is a antifungal reagent.
DC10698 Amoscanate Featured Amoscanate(nithiocyamine) is an experimental anthelmintic agent of the arylisothiocyanate class which was found to be highly effective in animals against the four major species of schistosomes which infect humans,and is also highly active against hookworm
DCAPI1158 Amoxicillin sodium (Amox) Amoxicillin sodium (Amox)
DCAPI1309 Ampicillin sodium Ampicillin is a beta-lactam antibiotic that is part of the aminopenicillin family.
DC23111 Ampkinone Ampkinone is a novel small molecule activator of AMPK, stimulates the phosphorylation of AMPK via indirect activation of AMPK in various cell lines (2.7-fold at 10 uM).
DC11274 AMPPD Featured AMPPD, 1,2-dioxo-cyclohexane derivatives, is a new biochemistry ultrasensitive alkaline phosphatase substrate.
DC23625 AMR-2 AMR-2 is a highly potent, orally active, triple reuptake inhibitor of SERT, NET, and DAT with IC50 of 3.0, 3.1, and 8.3 nM, respectively.
DC7002 Amrubicin(SM-5887) Amrubicin(SM-5887) is a novel anthracycline derivative for treatment of bladder carcinoma.
DC9634 Amsacrine Amsacrine (mAMSA) an antineoplastic agent which can intercalate into the DNA of tumor cells.
DC20088 Amuvatinib hydrochloride (MP470 hydrochloride; HPK 56 hydrochloride) Amuvatinib hydrochloride (MP470 hydrochloride) is a multi-targeted receptor tyrosine kinases inhibitor, which inhibits c-Kit (D816V), c-Kit (D816H), c-Kit (V560G), c-Kit (V654A), PDGFRα (D842V), and PDGFRα (V561D) with IC50s of 950 nM, 10 nM, 34 nM, 127 n
DC21995 AMXT-1501 AMXT-1501 (AMXT 1501, AMXT1501) is a novel potent polyamine transport inhibitor, synergistically reduces cell viability in NB cells in combination of with DFMO.
DC21996 AMXT-1501 tetrahydrochloride AMXT-1501 tetrahydrochloride (AMXT 1501, AMXT1501) is a novel potent polyamine transport inhibitor, synergistically reduces cell viability in NB cells in combination with DFMO.
DC23109 AMZ30 AMZ30 is a potent, selective, covalent inhibitor of the serine hydrolase protein phosphatase methylesterase-1 (PME-1) with IC50 of 0.6 uM, >100-fold selectivity over other SHs.

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