• 한국식품영양과학회지
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• 제44권9호
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• pp.1295-1303
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• 2015

국내에서 주로 재배되는 대표적인 베리류에 대한 화학 조성 및 기능성을 알아보고자 일정 시기에 수확한 오디, 블랙라즈 베리, 라즈베리, 블루베리의 pH, 산도, 유리당, ${\gamma}-aminobutyric$acid(GABA), 무기질 함량, phenolic compound, 항산 화 활성을 조사하여 비교하였다. 베리류 4종의 pH는 3.3~5.2로 블루베리가 가장 낮았고 오디가 가장 높은 반면, 산도는 0.26~1.10%(w/w)로 오디가 가장 낮았고 블랙라즈 베리가 가장 높았다. 베리류에서 검출된 유리당인 fructose와 glucose는 같은 비율로 존재하였고, 그 총량은 4.80~12.93%(w/w)로 오디가 가장 높았으며 블랙라즈베리가 가장 낮았다. GABA는 오디에 69.3 mg/100 g이 함유되어 있었는데, 이는 다른 베리류에 비해 3배 이상 많은 양이다. 베리류에 함유된 주요 무기질은 칼륨, 칼슘, 마그네슘이었고, 총 무기질 함량은 92.9~256.0 mg/100 g으로 블랙라즈 베리에 유의적으로 높게 함유되어 있었으며(P<0.05) 블루베리가 가장 낮았다. Total polyphenol과 total flavonoid 함량은 각각 198.2~547.2 mg/100 g과 5.0~94.6 g/100 g의 범위로 블랙라즈베리가 가장 높았고, 라즈베리는 유의적으로 가장 낮았다(P<0.05). Total anthocyanin은 19.8~385.6 mg/100 g의 범위로 블랙라즈베리가 가장 높았고, 라즈베리가 유의적으로 낮았다(P<0.05). Total PA(phenolic acids)는 블랙라즈베리와 라즈베리에 각각 14.0 mg/kg과 5.9 mg/kg이 함유되어 있었는데 이는 오디에 함유된 50.4 mg/kg보다 낮았으며, 391.4 mg/kg으로 가장 높게 함유된 블루베리에는 PA의 대부분이 chlorogenic acid였다. 베리류 4종의 항산화 활성을 DPPH 및 ABTS free radical scavenging activity를 분석하여 Trolox equivalent 값으로 나타낸 결과 Trolox equivalent antioxidant capacity와 total polyphenol, total anthocyanin, total flavonoid 함량 과는 유의적인 양(+)의 상관관계(Pearson 상관계수 r${\geq}0.85$; P<0.01)를 나타내었고, 블랙라즈베리가 DPPH 및 ABTS 항산화 활성이 가장 우수하였다.

• Natural Product Sciences
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• 제13권3호
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• pp.268-271
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• 2007

Glutamate-induced oxidative injury contributes to neuronal degeneration in many central nervous system (CNS) diseases, such as epilepsy and ischemia. Bioassay-guided fractionation of the MeOH extract of the seeds of Alpinia katsumadai Hayata (Zingiberaceae) furnished three phenolic compounds, alpinetin (1), pinocembrin (2), and (+)-catechin (3). Compounds 2 and 3 showed the potent neuroprotective effects on glutamate-induced neurotoxicity and reactive oxygen species (ROS) generation in the mouse hippocampal HT22 cells. In addition, Compounds 2 and 3 showed significant DPPH free radical scavenging effect. These results suggest that compounds 2 and 3 could be the effective candidates for the treatment of ROS-related neurological diseases.

• Biomolecules & Therapeutics
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• 제17권4호
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• pp.412-417
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• 2009

In the course of screening for antioxidant compounds by measuring the radical scavenging effect on DPPH (1,1-diphenyl- 2-picrylhydrazyl), a total extract of the twigs of Vitex rotundifolia (Verbenaceae) was found to show potent antioxidant activity. Subsequent activity-guided fractionation of the methanolic extract led to the isolation of three iridoid compounds, 10-O-vanilloylaucubin (1), 10-O-p-hydroxybenzoylaucubin (2) and aucubin (3), two C-glycoside flavones, vitexin (4) and orientin (5), and a quinic acid derivative, 3,4-di-O-caffeoylquinic acid (6). Their structures were elucidated by spectroscopic studies. Among them, compounds 5 and 6 showed the significant antioxidative effects on DPPH free radical scavenging test. In riboflavin-NBT-light and xanthine-NBT-xanthine oxidase systems, compounds 5 and 6 exhibited the formation of the blue formazan in a dose-dependent manner. Compounds 5 and 6 showed better superoxide quenching activities than vitamin C.

• 생약학회지
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• 제17권1호
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• pp.49-54
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• 1986

To explore the biological activities of Thalictrum alkaloids, a study was initiated to investigate the alkaloidal constituents from T. fauriei, a species indigenous to Taiwan. Extensive fractionation of the ethanolic extract provided three known aporphines, (+)-oconovine (Ia), (+)-isocorydine (Ib), and (+)-corydine (Ic) from nonphenolic tertiary base fraction. From quaternary base fraction two new protoberberinium salts, thalifaurine (IIa), dehydrodiscretine (IIb), in addition to magnoflorine (III), were isolated. The structure of both new compounds were confirmed by total syntheses. Fractionation of phenolic bases yielded a dihydromorphinandienone, (-)-ocobotrine (IV), as well as a novel aporphine-pavine dimer, tentatively named EP-10. The structure of EP-10 was established by means of 2D NMR studies. Preliminary study indicated a weak activity of lyzing Hela cells, in vitro, for EP-10.

• 생약학회지
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• 제13권3호
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• pp.132-135
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• 1982

Three phenolic alkaloid compounds (A,B,C) were isolated from the roots of Thalictrum uchiyamai Nakai (Ranunculaceae). Compound A, a colorless crystalline substance $mp168^{\circ}$, $C_{11}H_{15}NO_2$ was identified to be corypalline (6-methoxy-7-hydroxy-N-methyl-1, 2, 3, 4-tetrahydroisoquinoline) which has been reported by Wu from Thalictrum rugosum. Compound B, $mp166^{\circ}$ and Compound C, $mp164^{\circ}$ were shown aromatic rings by UV, IR spectra and chiral center by CD.

• 한국응용곤충학회지
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• 제34권1호
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• pp.9-14
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• 1995

From a chemist's perspective, Scarabaeidae is one of the most exciting group of insects to work on the isolation, identification, and synthesis of sex pheromones because-as opposed to Lepidoptera, which by and large utilizes straight chain alcohols, aldehydes, and acetates-the pheromonal chemistry of scarab beetles is remarkably diverse. While species in the subfamily Rutelinae utilize pheromone constituents, which are presumably fatty acid derivatives, the more primitive species in the subfamily Melolonthinae use phenolic, amino acid derivative, and terpenoid compounds. Here, I discuss the recent advances we have accomplished in the identification of scarab sex pheromones with especial emphasis on their chemical diversity. Also, I discuss the potential role of these sex pheromones in insect pest management. Field tests revealed that, in contrast to what has been frequently observed in the Lepidoptera, the higher the dosage of sex pheromone loaded in the traps the greater the capture of scarab beetles. These data suggest that mass trapping is more likely to be useful for scarab pest management than mating distruption.

• Natural Product Sciences
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• 제15권1호
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• pp.17-21
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• 2009

Column chromatographic separation of the alcoholic extract from the roots of Berberis amurensis yielded eight phenolic constituents including six lignans, hanultarin (1), (-)-secoisolariciresinol (3), (+)-lyoniresinol (5), (+)-syringaresinol (6), (+)-syringaresinol-O-$\beta$-D-glucopyranoside (7), liriodendrin (8), and two phenylpropanoids, 4-glucosyloxy-3-methoxyphenyl trans-propenoic ethyl ester (2), trans-ferulic acid (4). The structures were determined on the basis of NMR spectroscopic data. All isolated compounds(1-8) were reported for the first time from this source. Compound 1 exhibited moderate cytotoxicity against four human cancer cell lines in vitro using sulforhodamin B bioassay.

• Natural Product Sciences
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• 제20권2호
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• pp.91-94
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• 2014

Column chromatographic separation of the MeOH extract from the tubers of Bletilla striata yielded seven phenolic components including four phenanthrenes, 3,7-dihydroxy-2,4-dimethoxyphenanthrene (1), 3,7-dihydroxy-2,4,8-trimethoxyphenanthrene (2), 9,10-dihydro-4,7-dimethoxyphenanthrene-2,8-diol (3), and 9,10-dihydro-1-(4'-hydroxybenzyl)-4,7-dimethoxyphenanthrene-2,8-diol (4) and three stilbenes, gigantol (5), 3',4"-dihydroxy-5',3",5"-trimethoxybibenzyl (6), and batatasin III (7). Their structures were determined on the basis of NMR spectroscopic data. Among them, compound 2, 3, and 6 were reported for the first time from this plant. The isolated compounds (1-7) were tested for cytotoxicity against four human tumor cell lines in vitro using a Sulforhodamin B bioassay.

• Natural Product Sciences
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• 제20권2호
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• pp.86-90
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• 2014

Phytochemical investigation of the 80% MeOH extract from the leaves of Hosta longipes resulted in the isolation of sixteen compounds (1 - 16). The structures of the compounds were elucidated by spectroscopic methods to be methyl 10,10-dimethoxydecanoate (1), methyl 10-hydroxy-8E,12Z-octadecadienoate (2), methyl coriolate (3), trans-phytol (4), phytene-1,2-diol (5), phyton (6), (3S,5R,6S,7E,9R)-7-megastigmene-3,6,9-triol (7), (3S,5R,6S,9R)-3,6,9-trihydroxymegastigman-7-ene (8), shikimic acid (9), p-coumaramide (10), trans-N-p-coumaroyltyramine (11), cis-N-coumaroyltyramine (12), tryptophan (13), thymidine (14), adenosine (15), and deoxyadenosine (16). Compound 1 was synthesized, but not yet isolated from natural source, and compounds 2-16 were isolated for the first time from this plant source.

• Archives of Pharmacal Research
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• 제27권2호
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• pp.164-168
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• 2004

The chromatographic separation of the MeOH extract of the aerial parts of Solidago virga-aurea var. gigantea $M_{IQ}$ . (Compositae) led to the isolation of six terpenoids and four phenolic compounds, trans-phytol (1), ent-germacra-4(15),5,10(14 )-trien-1$\alpha$-ol (2), $\beta$-amyrin acetate (3), ent-germacra-4(15),5,10(14)-trien-1$\beta$-ol (4), $\beta$-dictyopterol (5), oleanolic acid (6), kaempferol (7), kaempferol-3-O-rutinoside (8), methyl 3,5-di-O-caffeoyl quinate (9), and 3,5-di-O-caffeoyl quinic acid (10). Their structures were established by chemical and spectroscopic methods. Compounds 4, 5, and 10 showed moderate cytotoxicity against five cultured human tumor cell lines in vitro with its E $D_{50}$ values ranging from 1.52∼18.57 $\mu\textrm{g}$/mL.L.