22155-73-3

Basic information

• Product Name: (+)-(R)-oleuropeic acid
• Synonyms: (+)-(R)-oleuropeic acid
• CAS NO: 22155-73-3
• Molecular Weight: 184.235
• Mol File: 22155-73-3.mol

Chemical Properties

• CAS DataBase Reference: (+)-(R)-oleuropeic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-(R)-oleuropeic acid(22155-73-3)
• EPA Substance Registry System: (+)-(R)-oleuropeic acid(22155-73-3)

Safety Data

• Hazardous Substances Data: 22155-73-3(Hazardous Substances Data)

Upstream product

• 1616079-03-8 6-O-[(R)-oleuropeoyl]-1-O-[2-(1-hydroxy-4-oxo-2,5-cyclohexadien-1-yl)ethyl]-β-D-glucopyranose 
• 1616079-04-9 6-O-[(R)-oleuropeoyl]-1-O-[2-(1-hydroxy-4-oxocyclohexyl)ethyl]-β-D-glucopyranose 
• 7785-53-7 4R-α-terpineol 
• 1187303-40-7 1,6-di-O-[(R)-oleuropeyl]-β-D-glucopyranose 
• 76509-36-9 8-bromo-p-menth-1-en-7-oic acid 

Downstream Products

• 1187303-40-7 1,6-di-O-[(R)-oleuropeyl]-β-D-glucopyranose 
• 294856-66-9 cypellocarpin C 

Relevant articles and documents

Biotransformation of α-terpineol by: Alternaria alternata

α-Terpineol (1), the main volatile constituent in some traditional Chinese medicines, has been reported to be metabolized to 4R-oleuropeic acid by the larvae of common cutworms. The present study verified that α-terpineol could be converted to 4R-oleurope

Eucalmaidins A-E, (+)-oleuropeic acid derivatives from the fresh leaves of Eucalyptus maideni

Five new (+)-oleuropeic acid derivatives, eucalmaidins A-E (1-5), together with 12 known compounds (6-17), were isolated from the fresh leaves of Eucalyptus maideni. Structures of the new compounds were determined on the basis of spectroscopic analyses (H

Quinoid glycosides from Forsythia suspensa

Phytochemical investigation on Forsythia suspensa (Thunb.) Vahl afforded 10 compounds, including quinoid glycosides, lignan glycosides, phenylethanoid glycoside and allylbenzene glycoside together with 13 known ones. Their structures were established based on extensive spectroscopic data analyses, including IR, UV, HRESIMS, 1D NMR and 2D NMR. Absolute configurations were determined by ECD calculation method and chemical degradation. In addition, all compounds were evaluated for their antiviral activity against influenza A (H1N1) virus and several were further evaluated against respiratory syncytial virus (RSV) in vitro. Among them, two previously known compounds showed significant activities against RSV with EC50 values of 3.43 and 6.72 μM.