• 생약학회지
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• 제45권2호
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• pp.93-100
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• 2014

The Acer tegmentosum (3 kg) were extracted with boiled water and the freeze dried extract powder was partitioned with $CH_2Cl_2$, EtOAc, n-BuOH and $H_2O$, successively. From the EtOAc and n-BuOH fraction, six phenolic compounds were isolated through the silica gel, octadecyl silica gel and sephadex LH-20 column chromatography. On the basis of spectroscopic methods, such as $^1H$-NMR and $^{13}C$-NMR, and LC/MS, the chemical structures of the compounds as feniculin (1), avicularin (2), (+)-catechin (3), (-)-epicatechin (4), salidroside (5) and 6'-O-galloylsalidroside (6). In this study, compounds 1 and 2 have been first isolated from the A. tegmentosum. To provide insight into the effects of six compounds isolated from A. tegmentosum on inflammation, we investigated its effect on nitric oxide (NO) production in RAW 264.7 cells using lipopolysaccharide (LPS) stimulation. Compounds 1 and 6 slightly repressed NO production. Also, compounds 3 and 4 inhibited NO secretion with statistical significance. However, compounds 2 and 5 did not show any inhibitory effect on NO production.

• 한국잡초학회지
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• 제9권2호
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• pp.154-167
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• 1989

시호(柴胡)를 포함(包含)한 21종(種) 약용식물(藥用植物)의 여러추출액(抽出液)이 벼, 피, 상치의 발아(發芽)에 미치는 영향(影響)과 이들이 함유(含有)한 phenolic compounds 와 지방산(脂肪酸) 및 유기산(有機酸)의 구성(構成)과 함량(含量)을 조사(調査)한 결과(結果)는 다음과 같다. 1. 공시약용식물(供試藥用植物)의 수용(水溶) 및 알코올추출액(抽出液)의 발아억제효과(發芽抑制效果)는 상치에 대(對)해 현저(顯著)하여 공시재료중(供試材料中) 석창포(石菖蒲), 천궁(川芎), 부자(附子), 시호(柴胡), 생강(生薑)당귀(當歸), 산약(山藥), 아무(莪茂)의 수용추출(水溶抽出) 5%는 상치의 발아(發芽) 및 생육(生育)을 90% 이상(以上) 억제(抑制)하였고, 향부자(香附子), 천남성(天南星), 석창포(石菖蒲), 천궁(川芎), 시호(柴胡), 부자(附子), 아무(莪茂), 독활(獨活), 산약(山藥), 조약(鳥藥), 작약(芍藥)의 알코올추출액(抽出液) 2%는 상치 의 발아(發芽) 및 생육(生育)을 95% 이상 억제(抑制)하였다. 2. 추출용매(抽出溶媒)를 달리한 결과(結果) 공시재료(供試材料)의 용매(溶媒)에 따른 억제정도(柳制程度)는 차이(差異)를 보여 ethanol, ether, aceton, chloroform 의 순(順)을 나타냈으나 공시재료(供試材料) 모두 같은 경향(傾向)을 나타내지는 않았다. 3. 공시약용식물(供試藥用植物)로부터 분리(分離) 동정(同定)된 phenolic compounds 의 양(量)은 행인(杏仁) 30.6013 mg/g, 초조(草鳥) 29.1008 mg/g, 천궁(川芎) 27.2947 mg/g 순(順)으로 많았고 발아억제효과(發芽抑制效果)는 이들의 양(量)뿐만 아니라 구성(構成) phenolic compounds의 종류(種類)와 밀접(密接)한 관련(關聯)이 있는 것으로 추정(推定)된다. 4. 공시재료(供試材料)의 지방산(脂肪酸) 및 유기산함량(有機酸含量)과 구성(構成)도 억제효과(抑制效果)와 다소(多少) 관련(關聯)이 있는 것으로 나타마 억제효과(抑制效果)가 높았던 천궁(川芎)은 24.10 mg/g의 지방산(脂肪酸)과 21.04 mg/g 의 유기산(有機酸)을 함유(含有)하고 있었다. 특히 발아억제효과(發芽抑制效果)가 높았던석창포(石菖蒲), 천궁(川芎), 시호(柴胡) 등(等)은 oleic, linoleic, linolenic 같은 불포화지방산(不飽和脂肪酸)을 다량(多量) 함유(含有)하고 있었다.

• 한국해양바이오학회지
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• 제10권1호
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• pp.1-8
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• 2018

The objective of this study was to purify and characterize the ${\beta}-secretase$ inhibitor from enzymatic hydrolysates of blackfin flounder muscle, for development of a novel anti-dementia agent that may be used in the drug or functional food industries. ${\beta}-secretase$ inhibitory peptide was purified from various enzymatic hydrolysates of blackfin flounder muscle. Among six enzymatic hydrolysates, the Alcalase hydrolysate revealed highest ${\beta}-secretase$ inhibitory activity. Consecutive purification of the blackfin flounder muscle hydrolysate using Sephadex G-25 column chromatography and octadecylsilane C18 reversed phase HPLC techniques were used to isolate a potent ${\beta}-secretase$ inhibitory peptide composed of 5 amino acids, Leu-Thr-Gln-Asp-Trp (MW: 526.7 Da). The $IC_{50}$ value of purified ${\beta}-secretase$ inhibitory peptide was $126.93{\mu}M$. Results of this study suggest that peptides derived from blackfin flounder muscle may be beneficial as anti-dementia compounds in functional foods or as pharmaceuticals.

• 대한화학회지
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• 제57권4호
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• pp.476-482
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• 2013

Cyanopyridone was prepared by the condensation of cyanoacetamide, substituted arylaldehydes and malononitrile in presence of pipyridine. The structure of the synthesized compound CP 1-20 was assigned on the basis of elemental analysis, IR, $^1H$-NMR and mass spectroscopy. These compounds were also screened for antimicrobial activity. The Minimum Inhibitory Concentration (MIC) of all the synthesized compounds was compared with standard drugs.

• Archives of Pharmacal Research
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• 제13권4호
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• pp.306-309
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• 1990

The synthesis of 5-hyterocyclimethyl-2'-deoxyuridines (4a-f) has been accomplished by displacement reaction of 5-(bromomethyl)-3', 5'-di-O-acetyl-2'-deoxyuridine with heterocyclic compounds, followed by removal of acetyl protecting group with methanolic ammonia. The compoudns synthesized were evaluated the inhibitory effects on L1210 cell probiferation and antiviral activities against Herpes simplex virus type 1 (HSV-1) None of the compounds exhibited sufficient biological activities.

• 약학회지
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• 제45권6호
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• pp.588-590
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• 2001

Two flavanones, (2S) -2'-methoxykurarinones (1) and kurarinones (2) , were isolated from the ethyl acetate extract of the roots of Sophora flavescense Ait. Their structrures were elucidated using NMR, UV and IR spectral analysis. These compounds exhibited a moderate antimicrobial activities against Staphylococcus aureus, Staphylococcus epidermidis Pseudomonas Putida and a weak anti-fungal activity against Candida albicans.

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.373.2-373.2
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• 2002

In search for plant-derived cytotoxic compounds, it was found that the MeOH extracts obtained from Amanita pantherina(DC. ex Fr.) Krombh exhibited significant cytotoxic activity against human tumor cell line. The classical fractionation on the basis of the inhibitory activity upon the growth human tumor cell line. in vitro, and repeated column chromatography afforded several cytotoxic compounds from Amanita pantherina (DC, ex Fr.) Krombh. (omitted)

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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• pp.266.2-266.2
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• 2003

The seeds of Astragalus sinicus grows in Korea have been used for oriental traditional medicine as the remedies for inflammation. Eight flavonoids were isolated from the Seeds of Astragalus sinicus and studied its anti-inflammatory activity. Some flavonoid compounds showed significant nitrogen monoxide(NO) production inhibitory activity in IFN-${\gamma}$, LPS stimulated RAW 264.7 cell. There compounds also showed significant antioxidative in DPPH assay. (omitted)

• Natural Product Sciences
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• 제27권3호
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• pp.176-182
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• 2021

The phytochemical investigation of Broussonetia kazinoki roots led to the isolation of ten compounds, including six flavonoids (1-6), two lignans (7 and 8), and two coumarins (9 and 10) by comparing their ¹H and ¹³C NMR spectra with reference values. To the best of our knowledge, compounds 9 and 10 were isolated from this plant for the first time. Among the ten isolates, compounds 2, 4, and 6 exhibited inhibitory effects against lipopolysaccharide (LPS)-induced nitric oxide (NO) production in macrophage RAW264.7 cells with IC₅₀ values of 11.98, 10.16, and 24.06 μM, respectively. Furthermore, compounds 2, 4, and 6 reduced LPS-induced inducible nitric oxide synthase (iNOS) expression in a dose-dependent manner. Pre-incubation of cells with these compounds also significantly suppressed LPS-induced COX-2 protein expression. Compounds 2, 4, and 6 also showed cytotoxic activity against HL-60 cells with IC₅₀ values ranging between 46.43 and 94.06 μM.

• Archives of Pharmacal Research
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• 제20권5호
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• pp.496-500
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• 1997

A strong antioxidant activity, which was measured by the radical scavenging effect on 1, 1-diphenyl-2-picrylhydrazyl(DPPH) radical, was detected in the methanol extract of Salvia miltiorrhiza Bunge (Labiatae). By activity-directed fractionation, compounds 1 and 2 were isolated as antioxidant principles of S. miltiorrhiza. Compounds 1 and 2 were identified as dimethyl lithospermate and 3-(3, 4-dihydroxyphenyl)lactamide, respectively, on the basis of spectral data. The radical scavenging effect of compounds 1 and 2 on DPPH radical exceeded that of L-ascorbic acid which is a well known antioxidant. These two compounds also showed prominent inhibitory activity against free radical generation in dichlorofluorescein (DCF) method and cytoprotective effect against t-BHP in cultured liver cell.