(+)-Tranylcypromine-[d5] Hydrochloride, is the labelled analogue of Tranylcypromine. Tranylcypromine is a monoamine oxidase inhibitor.

Tubocurarine is a toxic alkaloid. It is an acetylcholine receptor (AChR)-blocking agent. Tubocurarine is now rarely used as an adjunct for clinical anesthesia because safer alternatives like cisatracurium and rocuronium.

(+)-U-50488 hydrochloride is the less active enantiomer of (±)-U-50488, which is an opioid receptor agonist.

(+)-UH 232 maleate is a dopamine D2 antagonist (Ki = 72.7 nM in a ligand binding assay; apparent KB = 14.5 nM in a cAMP accumulation assay) that preferentially effects on central dopamine autoreceptors. (+)-UH 232 maleate significantly promotes dopamine synthesis and turnover. (+)-UH 232 maleate is also a dopamine D3 partial agonist.

Viroallosecurinine is a natural alkaloid compound found in several plants.

Xanthoplanine isolated from the roots of Zanthoxylum armatum DC.

(+)-Zizaene is a useful research chemical used in the biosynthesis of sesquiterpene antibiotic albaflavenone.

(+)-ZK 216348 is a selective nonsteroidal glucocorticoid receptor (GR) agonist for the treatment of experimental colitis (IC50 values of 20, 20, and 80 nM for GR, Progesterone (PR) and Mineralocorticoid (MR) receptors, respectively). (+)-ZK 216348 exhibits antiinflammatory activity for both systemic and topical application, and shows no negative effects on intestinal epithelial migration or proliferation.

(+)-α-Dihydrotetrabenazine is an impurity of Tetrabenazine, which is a VMAT-2 inhibitor and has been found to be effective in the treatment of hyperkinetic movement disorder at some extent.

(+)-α-Dihydrotetrabenazine-[13C2,d6] is the isotope labelled analog of (+)-α-Dihydrotetrabenazine, which is a potent inhibitor of vascular monoamine transporter 2 (VMAT2) and an agent of significant interest for therapeutic and molecular imaging applications.

(+)-α-Dihydrotetrabenazine-[d6] is the isotope labelled analog of (+)-α-Dihydrotetrabenazine, which is a potent inhibitor of vascular monoamine transporter 2 (VMAT2) and an agent of significant interest for therapeutic and molecular imaging applications.

(+)-α-Methyl-β-alanine is a reactant for the chemoenzymatic assembly of cryptophycins as potent anticancer therapeutics.

(+)-α-Methylbenzylamine (-)-2,2-Dimethylcyclopropanecarboxylate is an intermediate in the synthesis of (R,R)-Cilastatin (C441120), which is a derivative of Cilastatin (C441100), prevents renal metabolism of penem and carbapenem antibiotics by specific and reversible dehydropeptidase I inhibition. Antibacterial adjunct.

(+)-β-Dihydrotetrabenazine is a potent inhibitor of vascular monoamine transporter 2 (VMAT2) and an agent of significant interest for therapeutic and molecular imaging applications.

(+)Gomisin M2 is a lignan isolated and purified form fruits of Schizandra chinensis which is is utilized for antitussive and tonic purposes in Oriental medicine.

(+/-) 2′-Hydroxy-1,1′-binaphthyl-2-yl phosphate is an optical isomer that is an analogue to 1,1′-Binaphthyl-2,2′-diyl Hydrogenphosphate which is used in fluorescene anisotropy as a measure of chiral recognition.

(+/-)-((endo, RS), RS) Biperiden Hydrochloride is derived from Dicyclopentadiene (D439350), which is used in the preparation of poly(ionic liquid) brushes, used in anti-bacterial and anti-biofouling applications. Also used in the preparation of copolymer structures in the synthesis of nanocapsules.

(+/-)-((exo, RS), RS) Biperiden Hydrochloride is derived from Dicyclopentadiene (D439350), which is used in the preparation of poly(ionic liquid) brushes, used in anti-bacterial and anti-biofouling applications. Also used in the preparation of copolymer structures in the synthesis of nanocapsules.

(+/-)-(cis)-Dorzolamide is an isomer of Dorzolamide. Dorzolamide is a carbonic anhydrase inhibitor. It is an anti-glaucoma agent, and acts by decreasing the production of aqueous humour.

(+/-)-1-(3-Amino-pyridin-2-yl)ethylamine is used in various asymmetrical organic syntheses. It is also used in the synthesis of β-3 adrenergic receptor agonists for application towards diabetes type 2.