Ammi majus

Enzyme characteristics have been examined for recombinant C4H proteins from several species, including those from P. crispum, P. vulgaris, Ammi majus, H. tuberosus, and Ruta graveolens Similar values toward cinnamate (2 to 10p,A/) are reported, and consistently high substrate specificity (although the values vary between studies). Only 4-coumarate is found as the in vitro product, with no detectable 2- or 3-coumarate production. ... [Pg.152]

Hiibner, S. et al.. Functional expression of cinnamate 4-hydroxylase from Ammi majus L. Phytochemistry, 64, 445, 2003. [Pg.202]

Acetylrhamnosyl)gentiobioside] Ammi majus aerial parts Umbelliferae 262... [Pg.771]

Singab, A.N.B., Acetylated flavonol triglycosides from Ammi majus L., Phytochemistry, 49, nil, 1998. [Pg.799]

O-Glucoside 2,4, 4- Trihydroxychalcone (isoliquiritigenin) C21H22O9 Ammi majus Umbelliferae 115... [Pg.1024]

The dried ripe fruits of Ammi visnaga (Umbelliferae/Apiaceae) have a long history of use in the Middle East as an antispasmodic and for the treatment of angina pectoris. The drug contains small amounts of coumarin derivatives, e.g. visnadin (Figure 3.40) (compare Ammi majus, a rich source of furocoumarins, page 146), but the major constituents (2-4%) are... [Pg.75]

Methoxsalen (xanthotoxin 8-methoxypsoralen) (Figure 4.36), a constituent of the fruits of Ammi majus (Umbelliferae/Apiaceae), is used medically to facilitate skin repigmentation where severe blemishes exist (vitiligo). An oral dose of methoxsalen is followed by long wave UV irradiation, though such treatments must be very carefully regulated to... [Pg.146]

Ammi majus, Angelica archangelica, Saposhnikovia divarkata (Apiaceae) [root] Laurus nobilis (bay leaf, laurel) (Lauraceae) [leaf]... [Pg.275]

Fagara spp., Ruta graveolens (Rutaceae), Ammi majus, Levisticum sp., Angelica archangelica,... [Pg.360]

Widespread in leaves Ammi majus (Apiaceae) widespread as glycosides in Brassicaceae, Lamiaceae, Fabaceae, Scrophulariaceae [aerial] ... [Pg.587]

Umbelliferone (= Dichrin A Hydrangin 7-Hydroxycoumarin Skimmetin) (coumarin) Terpene Artemisia capillari (Asteraceae), Ammi majus, Apium, Ferula, Heracleum, Pimpinella spp. (Apiaceae), Aegk marmelos, Citrus grandis (Rutaceae), Hydrangea paniculata (Saxifragaceae), Atropa belladonna (Solanaceae) [root] AR (bovine lens) (30) 14.5t... [Pg.648]

Amithiozone, 1013 Amitid, 346 Amitril, 346 Amitriptyline, 346 therapeutic drug monitoring, 107 Amitriptyline embonate, 346 Amitriptyline hydrochloride, 346 Amitrole, 344 Ammi majus, 758 Ammoidin, 758... [Pg.1197]

Ekiert, H. and Gomolka, E. (2000) Coumarin compounds in Ammi majus L. callus cultures. Pharmazie, 55, 684-7. [Pg.234]

Elgamal, M.H.A., Shalaby, N.M.M., Duddeck, H. and Hiegemann, M. (1993) Coumarins and coumarin glucosides from the fruits of Ammi majus. Phytochemistry, 34, 819-23. [Pg.234]

Hamerski, D. and Matern, U. (1988a) Elicitor-induced biosynthesis of psoralens in Ammi majus L. suspension cultures. Microsomal conversion of demethylsuberosin into (-l-)marmesin and psoralen. Eur. J. Biochem., 171, 369-75. [Pg.237]

Hamerski, D., Schmitt, D. and Matern, U. (1990) Induction of two prenyltransferases for the accumulation of coumarin phytoalexins in elicitor-treated Ammi majus cell suspension cultures. Phytochemistry, 29,1131-5. [Pg.237]

Hehmann, M., Lukacin, R., Ekiert, H. and Matem, U. (2004) Furanocoumarin biosynthesis in Ammi majus L. Cloning of bergaptol O-methyltransferase. Eur.. Biochem., 271, 932 0. [Pg.238]

Abdulla WA, Kadry H, Mahran SG, el-Raziky EH, el-Nakib S. Preliminary studies on the anti-schistosomal effect of Ammi majus L Egypt J BiUiarz 1978 4(l) 19-26. [Pg.328]

Kiistala R, Makinen-Kiljunen S, Heikkinen K, Rinne J, Haahtela T. Occupational allergic rhinitis and contact urticaria caused by bishop s weed Ammi majus). Allergy 1999 54(6) 635-9. [Pg.328]

Sassafras albidum (sassafras) Lauraceae (iaurei) Bishop s weed Ammi majus... [Pg.1620]

Active ingredients Roots are rich source (6-16%) of furanocoumarins (8-geranoxypsoralen, imperatorin, heraclenin, heraclenol) (Handa and Rao, 1970), sphondin, bergapten, candicanin, candicopimaric acid and xanthotoxol). These can be converted by a chemical process into xanthotoxin (1.5%). Roots are a major source of xanthotoxin after the seeds of Ammi majus. Roots also provide about 0.1% essential oil. [Pg.70]

Source Ammi majus. Molecular formula Cn He O 4. Molecular weight 202.17. Melting point 252 deg C. [Pg.91]

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