• 제목/요약/키워드: flavonoid derivative

검색결과 23건 처리시간 0.025초

Tetracycline과 Flavonoid의 간단한 유도체 합성에 관한 연구 (A Study on the Syntheses of Simple Analogs of Tetracycline and Flavonoid)

  • 김학원
    • 대한화학회지
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    • 제40권8호
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    • pp.549-556
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    • 1996
  • 항생물질 tetracycline(TC)과 여러 가지 다양한 활성도를 보이는 flavonoid화합물들의 단순유도체들(13, 25, 26, 27)을 새로운 벙법으로 합성하였다, 먼저, 1,3-cyclohexanedione 유도체로부터 분자내 benzoyl group의 이동 반응을 이용하여 TC의 A, D ring이 유사한 bicyclic compound 13를 합성하였고, 0-methoxy benzaldehyde로부터 TC의 A, C ring이 유사한 bicyclic compound, 25와 chromone을 모핵으로 하는 flavonoid유도체, 26과 27을 합성하였다.

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HPLC를 이용한 생체 시료중의 새로운 플라보노이드 유도체인 DA-6034의 분석 (Analysis of DA-6034, a New Flavonoid Derivative in Biological Fluids by HPLC)

  • 이종진;손미원;유무희;장민선;김원배;이강춘
    • 약학회지
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    • 제42권2호
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    • pp.149-152
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    • 1998
  • A high performance liquid chromatographic method was developed for the determination of DA-6034 in biological fluids using internal standard. Plasma containing DA-6034 and inter nal standard was extracted by liquid-liquid extraction at an acidic pH. After evaporation of the organic layer, the drug and internal standard were reconstituted with mobile phase and injected into the column. They were separated by high performance liquid chromatography on inertsil ODS II column at 334 nm. The detection limit of DA-6034 in plasma was 0.02 ${\mu}$g/ml. In this method, the range of recovery and coefficients of variation were 96-110% and 0.40-3.78%, respectively. There was no interference from endogenous substances. Urine and bile were analysed using the deproteinization method and the detection limit of DA-6034 was 1${\mu}$g/l.

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Xanthone and Flavonoid Derivatives from the Leaves of Maclura tricuspidata with Antioxidant and Anti-tyrosinase Activity

  • Jo, Yang Hee;Lee, Solip;Ryu, Se Hwan;Yeon, Sang Won;Turk, Ayman;Hwang, Bang Yeon;Lee, Mi Kyeong
    • Natural Product Sciences
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    • 제27권4호
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    • pp.234-239
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    • 2021
  • Masclura tricuspidata, also called as Cudrania tricuspidata, is one of the most common Moraceae family plants in East Asia. Its trivial name follows mulberry due to the similar morphology. Investigation of the bioactive constituents of M. tricuspidata leaves yielded a new xanthone derivative along with twenty known compounds through various chromatographic techniques. A new compound was defined as mascluraxanthone (3), a prenylated xanthone glucoside on the basis of 1D and 2D NMR and MS data. Twenty known compounds were identified as four xanthone derivatives (1-2 and 4-5), two flavans (6-7), six flavanol derivatives (8-13), a flavonone (14) and seven flavonol derivatives (15-21). Among the isolated compounds, flavanol and flavonoid derivatives with 3',4'-OH groups showed antioxidant and anti-tyrosinase activities. Conclusively, the leaves of M. tricuspidata are rich in aromatic compounds including xanthones and flavonoids. In addition, these constituents showed antioxidant and anti-tyrosinase potentials, which might be useful for oxidative stress related diseases.

Constituents of the Aerial Parts of Lonicera etrusca Growing in Saudi Arabia

  • Alqasoumi, Saleh I.;Al-Rehaily, Adnan J.;Abdel-Kader, Maged S.
    • Natural Product Sciences
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    • 제15권3호
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    • pp.121-124
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    • 2009
  • Phytochemical investigation of the aerial parts of Lonicera etrusca resulted in the isolation of three iridoids including two aglycones, loganin aglycone (log-1) (1) and lonicerin (log-2) (2), and the known common glycoside loganin (4). The study also afforded a coumarin derivative, 7-hydroxycoumarin (3), and a flavonoid glycoside, luteolin-7-O-$\beta$-D-glucoside (5). The structures were determined utilizing physical, chemical and spectral methods.

Free Radical Scavenger로서의 Plant Phenolics의 특성과 항산화 활성

  • 이정수;최홍식
    • 생명과학회지
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    • 제4권1호
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    • pp.11-18
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    • 1994
  • Plant phenolics은 식물 생체에 널리 분포되어 있으므로 매일 일정량이 식품으로 섭취되어지고 있으며, 이 물질들은 식품 외에도 일부 향신료 및 의약용으로 이용되어지고 있다. 본 논문에서는 plant phenolics이 free radical scavenger로서의 주요 작용을 포함한 항산화 메카니즘과 기타 항산화 특성, 그리고 plant phenolic계 free radical scavenger 물질인 flavonoids와 hydroxycinnamic acids 및 hydroxycinnamic acid derivatives의 항산화 활성과 구조 간의 관계에 초점을 두어 고찰하였다. 또한 주요 식물별 plant phenolics 물질의 특성과 항산화 활성에 대하여서도 검토하였다.

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새로운 플라보노이드 유도체인 DA-6034에 대한 유전독성에 관한 연구 (Genotoxicity Studies of DA-6034, a New Flavonoid Derivative)

  • 강병철;권은아;이나래;안병옥;김원배;이상구;이국현;정진호;성명훈
    • Toxicological Research
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    • 제18권4호
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    • pp.349-354
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    • 2002
  • Inflammatory bowel disease (IBD) is a multifactorial disorder with unknown etiology and pathogenesis. Eupatilin, a kind of flavonoids, has been known to be effective for chronic diarrhea in Korea. In this study, we have investigated the genotoxicity of DA-6034, a new synthetic derivative of Eupatilin, wing in vitro and in viuo system such as Ames reverse mutation test, chromosomal aberration test and micronucleus test. in Ames reverse mutation test, DA-6034 treatment at the dose range up to 5,000 $\mu\textrm{g}$/ plate did not induced mutagenicity in Salmonella typhimurium TA98, TA100, TA102, TA1535, TA1537 with and without metabolic activation. Any significant aberration wasn't observed in chinese hamster lung(CHL) fibroblast cells treated with DA-6034 at the concentration of 5, 2.5, 1.25 mg/ml both in the absence and presence of metabolic activation system. In mouse micronucleus test, no significant increase in the occurrence of micronucleated polychromatic erythrocytes was observed in ICR male mice orally administered with DA-6034 of the doses of 2.0, 1.0, 0.5 g/kg. These results indicate that DA-6034 has no mutagenic potential under the condition in this study.

Biosynthesis of Two Flavones, Apigenin and Genkwanin, in Escherichia coli

  • Lee, Hyejin;Kim, Bong Gyu;Kim, Mihyang;Ahn, Joong-Hoon
    • Journal of Microbiology and Biotechnology
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    • 제25권9호
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    • pp.1442-1448
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    • 2015
  • The flavonoid apigenin and its O-methyl derivative, genkwanin, have various biological activities and can be sourced from some vegetables and fruits. Microorganisms are an alternative for the synthesis of flavonoids. Here, to synthesize genkwanin from tyrosine, we first synthesized apigenin from p-coumaric acid using four genes (4CL, CHS, CHI, and FNS) in Escherichia coli. After optimization of different combinations of constructs, the yield of apigenin was increased from 13 mg/l to 30 mg/l. By introducing two additional genes (TAL and POMT7) into an apigenin-producing E. coli strain, we were able to synthesize 7-O-methyl apigenin (genkwanin) from tyrosine. In addition, the tyrosine content in E. coli was modulated by overexpressing aroG and tyrA. The engineered E. coli strain synthesized approximately 41 mg/l genkwanin.

2-Arylethenylchronlones유도체의 합성 및 항암활성 검색 (2-Arylethenylchromone Derivatives : Synthesis and Anticancer Activity)

  • 문창상;이경원;이지용;이재열;정봉영;이경태;이용섭
    • 약학회지
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    • 제47권6호
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    • pp.376-381
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    • 2003
  • 2-Arylchromones, also known as flavones, are among the most ubiquitous classes of natural products occurring in the plant kingdom. On the other hand, 2-styrylchromones are relatively scarce in nature and only a few compounds has been isolated from the blue-green algae species. Therefore, new 2-arylethenylchromone derivatives ( 4a∼n, 5a∼f) were synthesized by the aldol condensation of 2-methylchromone ( 3) with several aromatic aldehydes in order to evaluate their cytotoxicities using a MTT assay on three tumor cells. 2-Arylethenylchromone derivative 4a showed the significant cytotoxic activities on KB, HL-60 and P-388 cell lines with $IC_{50}$/ values of 25.2, 63.59 and 49.51 $\mu$M, respectively, indicating that 2-arylethenylchromone skeleton has a potential anti-tumor application.

Cytotoxic and Antibacterial Activities of Gossypin

  • Chamundeeswari, D.;Sukumar, Ethirajan;Amar, K.;Reddy, N. Brahmananda;Kumar, I. Anil;Chowdry, B.V.;Samatha, K.
    • Natural Product Sciences
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    • 제13권4호
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    • pp.300-303
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    • 2007
  • Gossypin, a naturally occurring polyhydroxy flavonoid, when subjected to in vitro cytotoxic screening against vero cell lines exhibited 68.75% inhibition at a concentration of $1000{\mu}g$. When tested against five bacteria and five fungi, the flavone derivative showed a moderate activity against Staphylococcus aureus and Escherichia coli, mild inhibition against Pseudomonas aerugenosa and Salmonella typhi and no activity against any of the tested fungi, in the concentrations studied.

Analysis of DA-6034. a New Flavonoid Derivative in Biological Fluids by Fluorescence Detector

  • Jang, Ji-Myun;Park, Kyung-Jin;Lee, Jong-Jin;Kim, Dong-Goo;Shim, Hyun-Joo;Son, Mi-Won;Kim, Dong-Sung;Kim, Soon-Hoe;Yoo, Moo-Hi
    • 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.403.2-403.2
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    • 2002
  • A high performance liquid chromatographic method was developed for the determination of DA-6034 in biological fluids using fluorescence detector. The method involved deproteinization of biological sample with the same volume of acetonitrile, 0.2M zinc sulphate. and 0.15M barium hydroxide. The aliquot of supernatant was injected onto Nova-pak C18 column and detected by fluorescence detector. Emission and excitation wavelength of detector were 336nm and 440nm. (omitted)

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