(±)-ML 209 is a RORγt inverse agonist with IC50 value of 460 nM. It has the potential to treat TH17-related autoimmune diseases.

(±)-Myristoylcarnitine chloride is a homolog of Acetylcarnitine Chloride, which is a weak cholinergic agonist. Acylcarnitines are important intermediates in lipid metabolism.

(±)-N-(2-Chloro-1-methylethyl)benzylamine Hydrochloride is an intermediate in the synthesis of (S)-Phenoxybenzamine Hydrochloride (P228000), which is an irreversible α-antagonist. Used in the treatment of hypertension, it has a relatively slow onset and prolonged effect when compared to alternative α-blockers.

(±)-N-(2,6-Dimethylphenyl)-1-iso-propyl-2-piperidinecarboxamide-[d7] is the labelled analogue of (±)-N-(2,6-Dimethylphenyl)-1-iso-propyl-2-piperidinecarboxamide, which is an impurity of Ropivacaine.

(±)-N-3-Benzylnirvanol is a racemic mixture of (+)-N-3-benzylnirvanol and (-)-N-3-benzylnirvanol. (+)-N-3-benzylnirvanol and (-)-N-3-benzylnirvanol are inhibitors of the cytochrome P450 (CYP) isoform CYP2C19 (Kis = 0.292 and 5.3 μM, respectively).

(±)-N-Formyl Octabase is an intermediate in the synthesis of (±)-3-Methoxy-17-methylmorphinan Hydrobromide (M329120), the racemic mixture of Dextromethorphan (D299445) and Levomethorphan (L375850). Dextromethorphan is an antitussive compound showing analgesic properties; used in cough medication formulations. Levomethorphan is an antitussive medicine, a narcotic and controlled substance.

A stable isotopic labelled analog of Napropamid. Napropamid is a selective systemic amide herbicide which is used against a number of annual grasses and broad-leaved weeds for inhibiting root development and growth.

(±)-Naproxen-[d3] is the labelled racemic of Naproxen, which is a non-selective COX inhibitor.

Potent and selective CXCR3 antagonist

(±)-Nicotine-D3 salicylate is a labelled isomer salt of nicotine, which is a potent parasympathomimetic stimulant.

(±)-Nipecotic acid is a nonselective GAT inhibitor that also induces GABA release through a process termed ‘heteroexchange. IC50 = 8, 38, 106 and 2370 μM for hGAT-1, rGAT-2, hGAT-3 and hBGT-1 respectively.

(±)-Nornicotine-[d4] is the labelled analogue of (±)-Nornicotine, which is a metabolite of Nicotine. Nicotine is a potent parasympathomimetic stimulant.

(±)-Norpseudoephedrine-[d3] hydrochloride is the labelled salt of Norpseudoephedrine, which is an alpha- and beta-adrenergic receptor agonist with sympathomimetic activity.

A homolog of acetylcarnitine chloride. Acetylcarnitine chloride is a weak cholinergic agonist. Acylcarnitines are important intermediates in lipid metabolism.

(±)-Palmitoylcarnitine chloride, a long-chain acylcarnitine with both intracellular and extracellular roles, has a wide range of biological actions including the inhibition of protein kinase C and cell membrane disruption.

(+/-)-pantoprazole-[13C] sodium salt sesquihydrate is the labelled salt hydrate of Pantoprazole, which is a gastic proton pump inhibitor. It could be used in the treatment of ulceration and some diseases induced by gastroesophageal reflux through influencing gastric acid secretion.

(±)-Pinoresinol is a natural lignan compound found in several plants.

(±)-PPCC oxalate is a selective sigma (σ) receptor ligand, which is noted to exhibit high affinity for σ1 and also binds at σ2 sites (Ki = 1.5 nM and 50.8 nM respectively).

(±)-Pramipexole-(N6-propylidene) is an intermediate used in the synthesis of (±)-Pramipexole (P700740), which is a racemic analogue of (S)-Pramipexole (P700755), a dopamine-D2-receptor agonist. Antiparkinsonian.

(±)-Procinolol is a beta adrenergic receptor antagonist.

(±)-Propionylcarnitine chloride is the homolog of acetylcarnitine chloride, which is used in the synthetic preparation of pure esters of dl-carnitine chloride with fatty acids.

(+/-)-Propoxyphene-[d11] is the labelled racemate of Propoxyphene, which is an opioid analgesic and a mu-opioid receptor agonist.

(±)-SDZ-201 106 is a diphenylpiperazinylindole derivative that prolongs the open state of cardiac voltage-gated Na+ channels. It has been shown to increase net Na+ influx and the activity of reverse mode Na+/Ca2+ exchange, which leads to an increase in intracellular Ca2+, as well as to partially inhibit the Na+ pump in cardiac myocytes.

Speciosin P can be synthesized from Hexagonia speciosa, which features Sonogashira coupling as a key step.

(±)-Talinolol is a β1-selective adrenoceptor antagonist well known for its cardioprotective and antihypertensive activity. By blocking β1-adrenergic receptors, talinolol delays the conduction of stimuli in the AV node, reduces the sino-atrial conduction time, and impedes the sinus node automaticity.

Silymarin is a mixture of natural compounds isolated from milk thistle and used as a herbal remedy. (±)-Taxifolin is a flavanonol contained in silymarin, as well as other plant extracts. It is the dihydro form of quercetin, a flavonol with antioxidant properties.

One of the isotopic labelled form of (±)-Tolterodine, which is an antimuscarinic agent and could be used against urinary incontinence.

Boc-(±)-trans-4-(2-methoxyphenyl)pyrrolidine-3-carboxylic Acid is a useful synthetic intermediate.

Boc-(±)-trans-4-(3-fluorophenyl)pyrrolidine-3-carboxylic Acid is used to prepare pyrrolidinylurea and pyrrolidinylthiourea compounds as TrkA kinase inhibitors.

Boc-(±)-trans-4-(3-trifluoromethyl-phenyl)-pyrrolidine-3-carboxylic Acid is used to synthesize ring-constrained boropeptide thrombin inhibitors. It is also used to prepare substituted 2H-isoquinolin-1-ones as potent Rho-kinase inhibitors.

Boc-(±)-trans-4-(4-bromophenyl)pyrrolidine-3-carboxylic Acid is used to prepare substituted 2H-isoquinolin-1-ones as potent Rho-kinase inhibitors.