Perilla

Perilla frutescens (L.) Britt. China 1-perilla, aldehyde, apigenin, luteolin, 3-p-coumarylglycoside-5-glucoside of cyanidin, 7-caffeyl-glucosides of apigenin and luteolin, anthocyanins.33-50 Antibacterial, antitussive, stomachic, antiseptic. [Pg.222]

Furan, 3-(4-methylpentanoyl) — see Perilla ketone Furan, 2-methylthio-mass spectrometry, 4, 583 Furan, 3-morpholino-2,5-diphenyl-reaotions... [Pg.631]

Perilla ketone — see Ketone, 3-furyl isopentyl Perillene synthesis, 4, 668 Perinones, 1, 327, 337 Periodinane, bromo-synthesis, 1, 571 Periodinane, difluoro-reactions, 1, 571 Periodinanes cyclic... [Pg.739]

Menhaden oil Neatsfoot oil Oleic acid Oleo oil Olive oil Palm oil Peanut oil Perilla oil Pine oil Rape seed oil Rosin oil Soya bean oil Sperm oil Tallow Tallow oil Tung oil Turpentine Whale oil... [Pg.187]

Cod liver oil Linseed oil Menhaden oil Perilla oil Corn oil Cottonseed oil Olive oil Pine oil Red oil Soya bean oil Tung oil Whale oil Castor oil Lard oil... [Pg.188]

Perillic aldehyde, Cj Hj O, is present in the essential oil of Perilla nankinensis. It has been examined by Semmler and Zaar, who isolated it from the oil by means of its sodium sulphite compound. Perillic aldehyde has the following characters —... [Pg.207]

Myrtenal, C oH, 0, is an aldehyde found in the oil of Perilla nankin-ensis, associated with perillic aldehyde. It is also formed by the reduction of myrtenol, an alcohol of the formula CjpH,gO, occurring in oil of myrtle leaves. Myrtenal has the following characters —... [Pg.208]

Linolenic acid Linseed oil, hemp seed oil, perilla oil Holarrihidine holarrhena antidy, senterica... [Pg.434]

Perilla frutescens Couette-type mitochondrial activity non-growth [102]... [Pg.152]

Goto, T., Takase, S., and Kondo, T., PMR spectra of natural acylated anthocyanins determination of stereostructure of awobanin, shisonin and violanin (Commelina communis, Viola tricolor, Perilla orimoides). Tetrahedron Lett, 27, 2413, 1978. Agrawal, P.K., NMR spectroscopy in the structural elucidation of ohgosaccharides and glycosides, Phytochemistry, 31, 3307, 1992. [Pg.505]

The stems of the plant Perilla frutescens var. acuta have yielded two new prenyl 3-benzoxepine derivatives, perilloxin 53 and dehydroperilloxin 54, whose structures were established by spectroscopic means. An in vitro cyclooxygenase-1 bioassay was used to guide the separation of these natural products, which possessed moderate inhibitory activities against this enzyme (IC50 values for 53 and 54 were 23.2M and 30.4M respectively) <00JNP403>... [Pg.351]

For example, sol-gel immobilised bioactive liquids such as cineol, camphor, menthol, evening primrose and perilla oil used to functionalise textiles afford either skin-friendly textiles with antimicrobial and antiallergic effects due to immobilised natural oils or textiles for therapeutic treatment of the respiratory tract by means of immobilised mixtures of high volatility natural agents such as eucalyptol, camphor and menthol.27... [Pg.109]

Acylation reactions can also be greatly improved in this way, with t-alkyl- or sec-alkyl-manganese reagents reacting with acid chlorides in excellent yields [123]. The related addition-elimination to 3-ethoxy-2-cyclohexenone is also improved, resulting after acidic aqueous workup in 3-methyl-2-cyclohexenone [125]. The perilla-ketone 126 was prepared in an improved yield using copper(I) catalysis (Scheme 2.58) [129]. [Pg.70]

Scheme 2.S8. Preparation of perilla-ketone using copper-catalyzed acylation.

Saito K, Kobayashi M, Gong Z, Tanaka Y, Yamazaki M (1999) Direct evidence for anthocyanidin synthase as a 2-oxoglutarate-dependent oxygenase molecular cloning and functional expression of cDNA from a red form of Perilla frutescens. Plant J 17(2) 181-189... [Pg.92]

NT416 Park, K. H., J. D. Park, K. H. Hyun, M. Nakayama, and T. Yokota. Brassino-steroids and monoglycerides with brassinosteroid-like activity in immature seeds of Oryza sativa and Perilla frutescens and in cultured cells of Nicotiana tabacum. Biosci Biotech Biochem 1994 58(12) 2241-2243. [Pg.361]

Hypotensive activity. Methanol (50%) extract of the dried rhizome, administered intravenously to rats at doses of 0.25 and 0.5 g/kg (dry weight of plant), was active ° k Hypothermic activity. Hot water extract of a mixture of Pinellia ternata (Tu), Magnolia obovata (Bk), Perilla frutescens (Aer), Zin ber officinale (Rh), and Poria cocos (Fr) (6, 3, 2, 1, and 5 g, respectively), adminis-... [Pg.535]

Figure 6.21. A naturally occurring 2,4-oxazolidinedione from roasted perilla seed.

Much of the information on ANS has come not from studies on enzyme extracts but from analysis of DNA sequences and recombinant proteins. Sequences for the ANS were first isolated using transposon generated mutant lines of A. majus and Z. mays They encoded proteins of 40 to 41 kDa that were found to have similarity to 20GDs, during a study on a nonflavonoid enzyme. This sequence-based identification was confirmed by the in vitro assay of the recombinant Perilla frutescens protein, and subsequent assays on recombinant ANS from a range of species that confirmed the requirement for Fe, 20G, and ascorbate. Sequence comparisons show that ANS is more closely related to flavonol synthase (FLS), another 20GD, than to F3H. [Pg.157]

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