Moexiprilat completely inhibits estrone-induced cardiac fibroblast growth.

N-Ethylaniline is used in qualitative and quantitative detection of carbohydrates.

Lansoprazole sulfide is an impurity of Lansoprazole -- a gastric pump inhibitor.

Dibenzylamine is a component of Potent neurogenic agent.

Azobenzene is a Photosensor molecule known to undergo reversible isomerization from trans to cis on illumination with photons of appropriate wavelength.

Phenylmercuric propionate is an Organometallic.

Free Cyanine3 carboxylic acid (Cy3? carboxylic acid analog), non-activated dye. Non-sulfonated reagent, with good solubility in organic solvents, and limited aquous solubility. The dye can be used as a non-reactive fluorophore, for control experiments, and for calibration.

L 655240 is a thromboxane and prostaglandin endoperoxide receptor antagonist.

Bis(2-ethylhexyl)hexanedioate is a diester resulting from the formal condensation of the carboxy groups of adipic acid with 2-ethylhexan-1-ol. It is used as a plasticiser in the preparation of various polymers.

Vapreotide is used in therapy of experimental pancreatic neoplasms in hamsters.

Chlorbenside (C13H10Cl2S), also known as chlorparaside and chlorsulfacide, is a pesticide. It is most commonly used as an acaricide being used to kill mites and ticks.

(R)-Amlodipine is the R isomer of Amlodipine --- a medication used to lower blood pressure and prevent chest pain.

IMS2186 is an anti-proliferative and anti-angiogenic agent. IMS2186 blocks the cell cycle at G2 and inhibits the production of PGE2/TNF-α. IMS2186 inhibits cell growth in vitro in tumor cells, non-transformed fibroblasts, and retinal pigment epithelial cells. IMS2186 inhibits angiogenesis (IC50 = 0.1 μM) and cell migration. Intraocular injection of IMS2186 could be a long-lasting effective treatment for CNV (choroidal neovascularization) in AMD (age-related macular degeneration) with a reduction in scarring and related visual loss.

Tribenoside in conjunction with lidocaine can be used to treat hemorrhoids.

Lufenuron is a chitin-synthesis inhibitor.

Tributyl phosphite is an alkylphosphite and is reported to inhibit carboxylesterase activity.

Tributylamine is a biochemical.

PEG8-Tos is a PEG derivative containing a hydroxyl group with a tosyl group. The PEG linker contains 7 units of ethylene glycol. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The tosyl group is a very good leaving group for nucleophilic substitution reactions.

Tri(t-butoxycarbonylethoxymethyl) ethanol is a branched PEG derivative with a terminal hydroxy group and three t-butyl esters. The hydroxy group enables further derivatization or replacement with other reactive functional groups. The t-butyl protected carboxyl groups can be deprotected under mild acidic conditions.

m-PEG1-NHS ester is a PEG derivative containing an NHS ester. The NHS ester can be used to label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The hydrophilic PEG spacer increases solubility in aqueous media.

Edetol is an ingredient of anti-aging cosmetics; sensitive coating on piezoelectric crystal detectors of SO2.

Sulfo-SANPAH Crosslinker, or N-Sulfosuccinimidyl-6-[4'-azido-2'-nitrophenylamino] hexanoate is a water soluble, heterobifunctional protein crosslinker with a spacer arm length of 18.2 angstroms.

Hydroxyzine pamoate is an histamine H1 receptor antagonist that is effective in the treatment of chronic urticaria, dermatitis, and histamine-mediated pruritus. Unlike its major metabolite CETIRIZINE, it does cause drowsiness.

Lomifylline is an inducer of Ca2±release from intracellular stores via the ryanodine receptor.

TT01001 is a mitoNEET ligand. It acts by improving diabetes and ameliorates mitochondrial function in db/db mice.

DDMU is a biochemical.

Phenethyl phenylacetate is a biochemical.

Atractyloside Potassium Salt is a natural inhibitor of ADP and ATP transport (AAT). It acts by binding specifically to the adenine nucleotide translocator in the inner mitochondrial membrane.

N,N'-Diphenylguanidine is a biochemical.

Dibemethine is active against chloroquinone-resistant Plasmodium falciparum and inhibit chloroquine transport via the P. falciparum chloroquine-resistance transporter (PfCRT).