α-(Methylamino)isobutyric acid is a specific substrate for amino acid transport system A (ATA1). ATA mediate the uptake of short-chain neutral amino acids in a Na+-dependent manner.

L-2-Aminooxy-3-phenylpropanoic acid hydrobromide is a potent inhibitor of L-phenylalanine ammonia-lyase.

Glycyl-Exatecan (D5 hydrochloride) is deuterium labeled Glycyl-Exatecan hydrochloride.

NOC-5 is a diazeniumdiolate compound that belongs to the same family of NO donors.

4-Methylumbelliferyl-α-D-galactopyranoside (4MU-α-Gal), a substrate for α-galactosidase A (GLA), is a blue pro-fluorogenic substrate. 4-Methylumbelliferyl-α-D-galactopyranoside forms two products, galactose and fluorescent 4MU, upon cleavage by GLA.

Ferroheme, a complex of ferrous iron and a porphyrin, is an isosteric inhibitor of fatty acid binding to rat liver fatty acid binding protein.

GSK1820795A as a telmisartan analog is a selective antagonist at hGPR132a. GSK1820795A blocks activation of yeast cells expressing hGPR132a by N-acylamides.

Golgicide A-1 (GCA-1) is a less active cis-diastereomer of Golgicide A (GCA). Golgicide A-1 weakly inhibits mosquito reproduction.

A small molecule inhibitor of clathrin terminal domain and inhibits clathrin-mediated endocytosis.

QLT0267 is an ATP-competitive selective inhibitor of integrin-linked kinase (ILK).

CTP354, also known as C-21191, a novel deuterated subtype-selective GABA(A) modulator. CTP may be potentially useful for treatment of neuropathic pain, spasticity and anxiety disorders. GABAA receptors are found in the nervous system and, when activated, reduce the transmission of certain nerve signals. Several classes of widely used drugs target GABAA receptors, including benzodiazepines, but do not have the receptor subtype selectivity of CTP-354.

HPK1-IN-2 is a potent and orally active inhibitor of hematopoietic progenitor kinase-1 (HPK1, a serine/threonine Ste20-related protein kinase), Lck and Flt3 with IC50 of <0.05 μM, IC50 of <0.5 μM and IC50 of <0.05 μM, respectively. HPK1-IN-2 exhibits antitumor activity.

Stachyose hydrate act as a prebiotic to enhance the growth and activity of beneficial bacteria. Stachyose hydrate exhibit a hypoglycemic effect, and improve inflammation through modulating gut microbiota.

Sodium carboxymethyl cellulose (CMC-Na) (MW 250000) is the sodium salt of cellulose arboxymethyl and frequently used as viscous agent, paste and barrier agent.

Vindolinine is a natural alkaloide that can be found in Catharanthus roseus.

Neoisoastilbin possesses antioxidant, anti-hyperuricemic and anti-Inflammatory activities.

Kaempferol-3-O-(2''-O-β-D-glucopyl)-β-D-rutinoside is a natural glycoside that could be found in Camellia oleifera seeds.

Cantleyoside is a natiural iridoid glycoside that could be found in the Roots of Dipsacus asper.

Brandioside is a natural phenylpropanoid glycoside from Brandisia hancei.

Bletilol B is a natural compound that could be found in Bletilla striata.

Bletilloside A is a natural glucoside that could be found in the tubers of Bletilla striata.

Bisabolol oxide A possesses antihyperalgesic and antiedematous effects with oral activity.

Bergaptol O-β-D-glucopyranoside possesses anti-gastric ulcer and anti-cancer effect.

Azedarachol possesses antifeedant activity.

Arundinin is a stilbenoid from Bletilla striata.

Argentinogenin is a natural compound with anti-cancer activity that could be found in traditional Chinese drug Chan Su.

Ardisicrenoside A exhibits anti-cancer activity.

Anthranoyllycoctonine is a natural norditerpenoid alkaloid that could be found in the Leaves of Delphinium ajacis.

Angenomalin is a furanocoumarin from Angenlica anomala.

Angeloylgomisin Q is a new dibenzocyclooctadiene lignan from the stems of Schisandra sphaerandra. Angeloylgomisin Q has the potential for alzheimer's disease research.