Diphenyl cresyl phosphate is a biochemical.

Lofepramine is an antidepressant; serotonin and norepinephrine re-uptake inhibitor (SNRI). A psychotropic IMIPRAMINE derivative that acts as a tricyclic antidepressant and possesses few anticholinergic properties. It is metabolized to DESIPRAMINE. Lofepramine is a third generation tricyclic antidepressant utilized throughout Europe and Japan for the treatment of major depression.

C.I. Pigment Red 4 mainly used in printing ink, paint, watercolor, paint and inkpad color, also can be used for rubber, natural raw lacquer, cosmetics, paint and coating printing color. Yellow red powder, bright color. Insoluble in water, slightly soluble in ethanol, acetone and benzene. In concentrated sulfuric acid to blue light magenta, dilution after yellow red precipitation; In concentrated nitric acid for brilliant scarlet; In a dilute sodium hydroxide solution does not change color; In the ethanol – potassium hydroxide solution for purple. Liquidity and cover resistance, good heat resistance is poor.

C.I. 12170 is also known as Naphthylamine Bordeaux, (diluted with Barium Sulfate).

Dacuronium bromide is an aminosteroid neuromuscular blocking agent Pancuronium (P178500) with much weaker activity which was never marketed. It acts as a competitive antagonist of the nicotinic acetylcholine receptor (nAChR).

(S)-Laudanosine is the (S) enantiomer of laudanosine, a metabolite of the neuromuscular blocking agents atracurium and cisatracurium. It inhibits prolyl endopeptidase and inhibits both arachidonic acid- and collagen-induced aggregation in washed rabbit platelets.

Avenaciolide is a water-insoluble fungal metabolite that inhibits glutamate transport in isolated rat liver mitochondria.

Erythromycylamine is a macrolide antibiotic and an active metabolite of dirithromycin. It is active against a variety of bacteria, including strains of S. pyogenes, S. pneumoniae, L. monocytogenes, and B. pertussis. It is also active against 28 clinical isolates of M. avium complex (MAC) isolated from patients with AIDS. Erythromycylamine inhibits polylysine and polyproline synthesis in a cell-free assay.

Phomalactone is a fungal metabolite that is active against various strains of plant pathogenic fungi.

Reparixin L-lysine salt is a potent and noncompetitive CXCR1 and CXCR2 allosteric antagonist that inhibits migration of neutrophils induced by CXCL1, CXCL2, CXCL8 and CINC-1. This product also inhibits vascular permeability and neutrophil recruitment in in vivo models of mild and severe ischemia/reperfusion injury. Also selectively depletes cancer stem cells in human breast cancer cell lines and xenograft models.

Pyruvic acid semicarbazone is a biochemical.

Camptothecin sodium selectively inhibits the nuclear enzyme DNA Topoisomerase, Type I. Several semisynthetic analogs of camptothecin have demonstrated antitumor activity.

Profluralin is an herbicide.

Aureothin is a natural nitroaryl-substituted polyketide that exhibits antitumor, antifungal, and insecticidal activities. It is a non-competitive inhibitor of NADH:ubiquinone oxidoreductase.

Muscimol is a neurotoxic isoxazole obtained by decarboxylation of Ibotenic Acid. Muscimol is a potent agonist of GABA-A receptors and is used mainly as an experimental tool in animal and tissue studies.

Aseanostatin P1 is a fatty acid which inhibits myeloperoxidase (MPO) release from human polymorphonuclear leukocytes.

Amiloride is a medication typically used with other medications to treat high blood pressure or swelling due to heart failure or cirrhosis of the liver. In the USA, this drug is available via prescription only.

AM-1172 is an endocannabinoid analog specifically designed to be a potent and selective inhibitor of AEA uptake that is resistant to FAAH hydrolysis.

Glyceryl monooleate is a biochemical which may be used as a nanocarrier for drug delivery.

Bis-PEG3-sulfonic acid is a PEG Linker.

PEG3-bis(phosphonic acid) is a PEG Linker.

Azido-PEG2-CH2CO2-t-Bu is a PEG derivative containing an azide group and a t-butyl ester. The hydrophilic PEG spacer increases solubility in aqueous media. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The t-butyl protected carboxyl group can be deprotected under acidic conditions.

diethyl 12-bromododecylphosphonate is a non-PEG Linker.

diethyl 10-bromodecylphosphonate is a non-PEG Linker.

Hydroxy-PEG2-methylamine is a PEG derivative containing a hydroxyl group with a methylamine group. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The methylamine group is reactive with carboxylic acids, carbonyls (ketone, aldehyde) etc.

m-PEG1-acid is a PEG derivative containing a terminal carboxylic acid. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. The hydrophilic PEG spacer increases solubility in aqueous media.

NH-bis(PEG2-OH) is a branched PEG derivative with a central amino group and two terminal hydroxyl groups. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls, etc. The hydroxy groups enable further derivatization or replacement with other reactive functional groups.

PEG16 is a PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.

Hexaethylene glycol is a PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.

m-PEG10-alcohol is a PEG derivative containing a hydroxyl group. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The hydrophilic PEG spacer increases solubility in aqueous media.