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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC22371 | Rocuronium |
An aminosteroid non-depolarizing neuromuscular blocker or muscle relaxant used in modern anaesthesia. .
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| DC24005 | Apramycin |
An aminoglycoside antibiotic used in veterinary medicine..
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| DC21155 | Myriocin |
An amino fatty acid antibiotic that is 10- to 100-fold more potent than cyclosporin A as an immunosuppressive agent of the immune response in vitro and in vivo.
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| DC22827 | DBCO-NHS ester |
An amine-reactive NHS ester that provides easy attachment of the reactive moiety to almost any primary or secondary amine group, such as that of protein, peptide, or small molecule amine.
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| DC22888 | β2AR-IN-15 |
An allosteric, small-molecule negative modulator for β2AR with Kd of 1.7 uM.
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| DC23931 | Hydrastine |
An alkaloid of Hydrastis canadensis used in many dietary supplements intended to enhance the immune system.
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| DC24153 | Cysteamine hydrochloride |
An agent for the treatment of nephropathic cystinosis and an antioxidant.
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| DC22762 | Norendoxifen |
An active metabolite of the selective estrogen receptor modulator (SERM) tamoxifen.
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| 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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| 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.
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| DC9634 | Amsacrine |
Amsacrine (mAMSA) an antineoplastic agent which can intercalate into the DNA of tumor cells.
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| DC7002 | Amrubicin(SM-5887) |
Amrubicin(SM-5887) is a novel anthracycline derivative for treatment of bladder carcinoma.
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| 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.
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| 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).
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| DCAPI1309 | Ampicillin sodium |
Ampicillin is a beta-lactam antibiotic that is part of the aminopenicillin family.
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| DCAPI1158 | Amoxicillin sodium (Amox) |
Amoxicillin sodium (Amox)
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| 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.
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| DCAPI1067 | Ammonium Glycyrrhizinate (AMGZ) |
Ammonium Glycyrrhizinate (AMGZ)
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| DC9181 | Amlodipine Besylate |
Amlodipine besylate is a long-acting calcium channel blocker.
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| DC20206 | Amitriptyline;MK-230, N-750, Ro41575 |
Amitriptyline is a tricyclic antidepressant (TCA) with analgesic properties, widely used to treat depression and neuropathic pain.
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| 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.
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| DC11324 | Aminopeptidase N Inhibitor |
Aminopeptidase N (AP-N) inhibitor is a reversible inhibitor of AP-N/CD13 (IC50 = 25 μM).
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| DC8984 | Aminoglutethimide |
Aminoglutethimide is an aromatase inhibitor with IC50 of 10 μM.
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| DCAPI1043 | Amikacin hydrate |
Amikacin is an aminoglycoside antibiotic used to treat different types of bacterial infections.
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| DCAPI1263 | Amidopyrine |
Amidopyrine is white crystalline substance used as an analgesic and antipyretic.
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| 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.
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| DC12430 | AMG7703 |
AMG7703 (4-CMTB, AMG-7703) is an allosteric, selective agonist of FFAR2 (GPR43)..
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| 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).
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| DC20661 | AMG-1694 |
AMG1694 is a potent, small molecule Glucokinase (GK)-GKRP (GK regulatory protein) disruptor, does not block the GK binding site directly.
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| DC20660 | AMG-076 |
AMG-076 is a potent, selective, non-peptide antagonist of MCHR1 (Melanin-concentrating hormone receptor 1) with binding IC50 of 0.6 nM, with dramatically reduced hERG liability (IC50>5 uM).
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