All Products

or product name starting with: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

A 80915A is A semi-naphthoquinone antibiotic produced by Streptomyces aculeolatus....

A 80987 is an HIV-1 protease inhibitor.

A-80b is a synthesized pyridazino[4,5-b]indole derivate. A 80b shows potent and lo...

A 81282 is a non-peptide selective antagonist of angiotensin receptors. A-81282 lo...

A 81988 is a selective angiotensin II antagonist for type I receptors. It is a p...

A-83-01 is an ALK inhibibitor. It was found that A-83-01 inhibited the transcripti...

A 83016A is a kinamycin-type antibiotic; from an unidentified actinomycete designa...

A 83016F is an antibiotic from an actinomycete designated A83016. It exhibits weak...

A-834735 is a drug developed by Abbott Laboratories that acts as a potent cannabin...

A 83586C is a depsipeptide antibiotic from Streptomyces karnatakensis that shows p...

A-836339 is a drug developed by Abbott Laboratories that acts as a potent cannabin...

A839977 is a P2X7R antagonist.

A-841720 is a metabotropic glutamate receptor 1 antagonist.

A-849519 is a reversible inhibitor of MetAP2 that has demonstrated anti-angiogenes...

A-850002 is a bioactive chemical.

A-85380 HCl

A-85380 is a nicotinic acetylcholine receptor agonist.

A 85 4777 is an antiinflammatory agent with nonclassical immunosuppressive propert...

A-867744 is a type II PAM with good potency and selectivity. A-867744 showed accep...

A-875400 is an inactive enantiomer of A-908292 (GLXC-22078) with approximately 50-...

A-887826 is Nav1.8 channel blocker of TTX-resistant sodium currents in rat dorsal ...

A-893 is a potent and selective SMYD2 inhibitor (IC50: 2.8 nM). A cocrystal struct...

A-908292 is a novel acetyl CoA carboxylase 2 (ACC2) inhibitor with an IC(50) of 23...

A 9145C is an inhibitor of RNA methylase. It also inhibits cyclopropane fatty acid...

A-922500 is a potent orally active inhibitor of DGAT-1 activity, inhibiting both h...

A-923 is an H3 antagonist with effects on cognition.

A 924 is an antineoplastic amino acid derivative.

A-933548 is a potent Calpain inhibitor for the Treatment of Alzheimer's Disease. A...

A-935142 is a novel hERG channel activator.

A 9387 is an inhibitor of Tn3-encoded resolvase protein binding at the res site.

A939572 is is a potent and orally bioavailable inhibitor of stearoyl-CoA desaturas...

A-940894 is a potent histamine H4 receptor antagonist with anti-inflammatory prope...

A-943931 HCL

A-943931 is Potent and selective H4 antagonist. Potent and selective histamine H4...

A-953227 is a highly potent and selective inhibitors of calpain. A-953227 features...

A-966492 is a potent PARP inhibitor, which displayed excellent potency against the...

A-967079 is a potent and selective antagonist of Transient Receptor Potential Anyk...

A-967079 is a selective TRPA1 channel blocker.

A‑971432 is a potent, orally bioavailable, selective Sphingosine-1-Phosphate Rece...

A-9758 is a novel potent and selective inverse agonist of RORγt.

A-9758 is a novel potent and selective inverse agonist of RORγt.

A-987306 is a potent histamine H4 receptor antagonist that is selective for H3, H1...

AA10 TG2 inhibitor

AA10 is a irreversible transglutaminase 2 (TG2) inhibitor.

AA-115, also known as APG-115, is a highly potent, chemically stable and efficacio...

AA 193 is a selective inhibitor of the presecretory reabsorption of uric acid.

AA 2379 is an antiinflammatory agent. AA 2379 inhibits the vascular permeability ...

AA26-9 is a potent and broad-spectrum serine hydrolase inhibitor. AA26-9-inhibite...

AA-289 is a novel potent MDM2 degrader.

AA 31 is a biochemical.

AA41612 is a novel antagonist of melanopsin-mediated phototransduction.

AA43279 is a novel selective Nav1.1 activator, increasing the firing activity of p...

AA 497 (Free Base)

AA 497 is a beta-2 agonist. AA497 causes relaxation and suppresses Ca spike freque...