| DC22431 |
AM432 sodium |
AM 432 is potent, selective, orally active prostaglandin D2 receptor (DP2/CRTH2) antagonist with binding IC50 of 6 nM for hDP2. |
|
| DC23485 |
AM-5262 |
AM-5262 is a potent full GPR40 (FFA1) agonist with EC50 of 81 nM. |
|
| DC23435 |
AM-6226 |
AM-6226 (AM6226) is a potent, selective, orally bioavailable GPR40 (FFA1) full agonist with EC50 of 0.12 uM. |
|
| DC9447 |
AM679 |
AM679 is a potent and selective FLAP inhibitor with IC50s of 2.2 nM/0.6 nM/154 nM for FLAP binding/hLA/hWB respectively. |
|
| DC8958 |
Amantadine HCl |
Amantadine Hydrochloride is an antiviral and an antiparkinsonian drug. |
|
| DC10372 |
Amcasertib(BBI503)
Featured
|
Amcasertib(BBI503) is an orally administered investigational agent designed to inhibit cancer stem cell pathways, including Nanog, by targeting stemness kinases. |
|
| DC20792 |
Amelubant |
Amelubant (BIIL284) is a potent, long-acting, orally active leukotriene B4 (LTB4) receptor antagonist, inhibits LTB4-induced mouse ear inflammation with ED50 of 0.008 mg/kg (p.o.). |
|
| DC7356 |
Ametantrone
Featured
|
Ametantrone is a new anthracenedione antineoplastic agents, produced a concentration-dependent inhibition of hepatic microsomal lipid peroxidation. |
|
| DC9457 |
AMG 837 (calcium hydrate) |
AMG 837 calcium hydrate is a potent GPR40 agonist(EC50=13 nM) with a superior pharmacokinetic profile and robust glucose-dependent stimulation of insulin secretion in rodents.
|
|
| 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). |
|
| 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) |
|
