B. Hordenine:
Synonyms Anhaline; Eremursine; Peyocactine.
Biological Sources It is obtained from the plant of Lophophora williamsii (Lamaire) Coult. (Catctaceae) (Peyote) and Selenicereus grandiflorus Britt and Rose (Coctaceae) (Night Blooming Cereus).
Chemical Structure
4-[2-Dimethylamino) ethyl] phenol; (C10H15NO).
Isolation It is isolated from barley germs by the method suggested by Erspamer and Falconieri* (1952).
Characteristic Features
1. It is obtained as orthorhombic prisms from ethanol or benzene +ether; as needles from water having mp 117-118°C.
2. It sublimes at 140-150°C and has a bp11 173°C.
3. Solubility Profile: It is very soluble in chloroform, ethanol and ether; 7 g dissolves in 1 L of water; practically insoluble in petroleum ether; and sparingly soluble in benzene, xylene and toluene.
Identification Test Hrodenine readily forms its hydrochloride salt which is obtained as needles from ethanol having mp 177°C; and it is very soluble in water.
Uses It exhibits digitalis-like activity.
Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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