The chemical substance known as (+)-threo-1-phenyl-2-decanoylamino-3-morpholino- is characterized by its specific stereochemistry and functional groups. It features a threo configuration, indicating a particular arrangement of substituents around the chiral centers, which influences its biological activity and interactions. The presence of a phenyl group suggests potential aromatic characteristics, while the decanoyl group contributes to its hydrophobic properties, affecting solubility and membrane permeability. The morpholino moiety enhances the compound's ability to interact with biological targets, potentially influencing its pharmacological profile. This compound may exhibit properties relevant to medicinal chemistry, particularly in the development of therapeutic agents. Its CAS number, 80938-69-8, allows for precise identification in chemical databases, facilitating research and application in various fields, including drug development and biochemical studies. Overall, the unique combination of structural features in this compound suggests it may have significant implications in pharmacology and biochemistry.

(+)-threo-1-phenyl-2-decanoylamino-3-*morpholino-

80938-69-8: DL-threo-PDMP, HCl, N-[(1R,2R)-2-hydroxy-1-(morpholin-4-ylmethyl)-2-phenylethyl]decanamide hydrochloride

Applications DL-threo-PDMP can deplete cells and mice of their glucosphinolipids.
References Abe, A., et. al.: J. Biochem., 111, 191 (1992)


DL-threo-PDMP

PDMP-d8

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CAS 80938-69-8: (+)-threo-1-phenyl-2-decanoylamino-3-*morpholino-

DL-threo-PDMP

Ref: TR-P217390

PDMP-d8

Ref: TR-P217392

(±)-threo-1-Phenyl-2-decanoylamino-3-morpholino-1-propanol hydrochloride

Ref: 3D-FDA93869