Cissampelos

Troupin has also been reported . These alkaloids were found to exhibit antimicrobial and antiplasmodial activities. Epinetrum villosum is a twining liana, growing in secondary forests in the coastal areas in Congo and Angola and is used in traditional medical for the treatment of fever, malaria and dysentery . The genus Cissampelos contains cissampareine, which has potential medicinal uses, but it is also psychoactive. It is a principal alkaloid of dawidjiewortel (Cissampelos capensis), which grows in South Africa. [Pg.46]

Ramirez, I. et al., Cissampeloflavone, a chalcone-flavone dimer from Cissampelos pareira. Phytochemistry, 64, 654, 1421 (Frratum), 2003. [Pg.1064]

Cissampelos pareira L. Xi Sheng Teng (Ice vine) (plant) Cissampareine, hayatine, pelosine, isoquinoline, hayatinine, berberine, dl-beheerine, dl-curine, D-guereitol, d-isochondrodendrine, hayatidine, cissamine, menisnine, reserpine, cissampeline.33-450 Blockade of NMJ depolarization. Used externally on wound surfaces to relieve pain. [Pg.54]

Ipomoea cairica (L.) Sweet Evodia rutaecarpa (Juss.) Berth Cissampelos pareira L. [Pg.370]

Citrus aurantium, Liquidambar orientalis, L. styraciflua, Lycium barbarum, L. pallidum, Populus alba, Rheum officinale, R. palmatum, R. tanguticum, Styrax benzoin Blumea balsumifera Liquidambar orientalis, L. styraciflua Erythroxylum coca Cissampelos pareira... [Pg.510]

Chelidonium majus (Papaveraceae) phy 26,3235 87 Cissampelos pareira (Menispermaceae) phy 26,3235 87 Corydalis cava (Papaveraceae) phy 26,3235 87 Corydalis meifolia (Papaveraceae) tet 42, 675 86 Eschscholzia californica (Papaveraceae) phy 26, 3235 87 Eschscholzia lobbii (Papaveraceae) phy 26,3235 87 Fumaria parviflora (Papaveraceae) phy 26, 3235 87 Papaver somniferum (Papaveraceae) phy 26, 3235 87 Thalictrum dipterocarpum (Ranunculaceae) phy 26, 3235 87 Thalictrum flavum (Ranunculaceae) phy 26,3235 87 Thalictrum foetidum (Ranunculaceae) phy 26, 3235 87 Thalictrum rugosum (Ranunculaceae) phy 26,3235 87... [Pg.143]

Adonis spp. (Ranunculaceae) cccc 52,804 87 Annona cherimolia (Annonaceae) jnp 48,151 85 Ayuilegia spp. (Ranunculaceae) cccc 52, 804 87 Aristolochia clematitis (Aristolochiaceae) cccc 52,804 87 Caltha palustris (Ranunculaceae) cccc 52, 804 87 Chelidonium majus (Papaveraceae) pm 60, 380 94 Cissampelos pareira (Menispermaceae) fit 63, 282 92 Clematis recta (Ranunculaceae) cccc 52, 804 87 Consolida regalis (Ranunculaceae) cccc 52, 804 87 Corydalis dasyptera (Papaveraceae) tcyyk 9,37 97 Corydalis gortschakovii (Papaveraceae) cnc 13,702 77 Corydalis nobilis (Papaveraceae) cccc 54,2009 89... [Pg.153]

These alkaloids were isolated, along with their unsaturated analogs (see Section II,B,4), from Cissampelos ovalifolia D.C., an alleged component of Mac-ushi curare, and characterized in 1970 by chemical interrelation and MS studies. At that time it was shown that the three bases have the same skeleton,... [Pg.9]

These alkaloids, also from Cissampelos ovalifolia D.C., show a mode of MS cleavage somewhat different from that of the dihydro bases (Section II,B,3) with principal scissions at a, b, c, and d. Diazomethane converted both 37 and 38 to 39 (27). MS data alone did not allow a choice between possible isomers, so X-ray work was done on methylwarifteine (38) (22) and dimethylwarifteine (39) (23). The structures of these bases, and therefore of warifteine (37), are as shown. Dimethylwarifteine is identical to O-methylcissampareine, isolated from Cissampelos pareira Linn (27). This family of alkaloids is unusual in having a benzyloxy bridge. [Pg.10]

Guatteria megalophylla Diels (Annonaceae) afforded (/ ,/ )- , 0-dimethylcur-ine (144), C38H42N206, mp 133-136°C (EtOAc-cyclohexane), identified by UV, NMR, MS, and ORD, and by comparison with a sample synthesized by CH2N2 methylation of (/ ,/ )-l2 -0-methyIcurme (145, Section II,C,64), also isolated from this plant (82). (/ ,/ )-< ,0,-Dimethylcurine had been prepared by methylation of (/ ,/ )-curine (75) (83), but was not previously reported in nature however, (5,S)-0,0-dimethylcurine is a known alkaloid of Cissampelos pareira (84). [Pg.35]

Methylation (CH2N2) of the alkaloid gave the known (R,./ )-dimethylcurine (144). Since by MS of 145 and 213 the tetrahydroisoquinoline ring bonded by an ether linkage to an unsubstituted p-tolyloxy contains a free OH, and this OH has no free ortho or para positions for deuterium exchange, the structure of 12 -0-methylcurine was proven (82). (R,R)-12 -0-Methylcurine is the enantiomer of (+, + )-4"-0-methylcurine, reported from Cissampelos pareira in 1966 (84). [Pg.56]

Cissampelos pareira Linn." (roots) Menispermaceae Monomethyltetrandrinium (7) ( + )-Tetrandrine (4,47)... [Pg.2]

Investigation of the Thai folk medicine, krung kha mao, the roots of Cyclea barbata Miers (formerly identified as Cissampelos pareira L.), has yielded many bisbenzylisoquinolines. other alkaloids d/-tetrandrine, isotetrandrine, limacine, berbamine, and homoaromoline (4,5). From the same plant, d/-fangchinoline, thalrugosine (d-isofangchinoline) (6), and the... [Pg.6]

Tetrandine (bisbenzvlisoquinoline) Cissampelos pareira, Stephania tetrandra (Menispermaceae) ACE [70]... [Pg.578]

Cissampelos pareira, Cyclea peltate, Stephania tetranda,... [Pg.148]

Cissampelos pareira, Cycka peltata, Stephania discolor, S. tetranda (Menispermaceae)... [Pg.214]

Calycocarpum (calycocarpum) Chondrodendron (chondrodendron) Cissampelos (cissampelos)... [Pg.2254]

C. marschalliana Cissampelos pareira Glaucium ftavum Cissampelos pareira Corydalis cava ... [Pg.155]

See also in sourсe #XX -- [ Pg.142 ]

See also in sourсe #XX -- [ Pg.4 , Pg.4 , Pg.4 , Pg.5 , Pg.7 , Pg.7 , Pg.7 , Pg.9 , Pg.13 ]

See also in sourсe #XX -- [ Pg.120 , Pg.244 , Pg.256 ]

See also in sourсe #XX -- [ Pg.54 ]

See also in sourсe #XX -- [ Pg.10 ]

See also in sourсe #XX -- [ Pg.53 ]

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