• 제목/요약/키워드: COSY$

검색결과 158건 처리시간 0.029초

On The Chemical, Botanical, and Chemotaxonomical Evaluation of The Genus Citrus -Part I : Polymethoxyflavones of The Leaf of Citrus deliciosa Ten.-

  • El-Domiaty, Maher M.;Abdel-Aal, Mahmoud M.;El-Shafae, Azza M.
    • Natural Product Sciences
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    • 제2권2호
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    • pp.106-114
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    • 1996
  • Four polymethoxyfavones were isolated from the leaves of Citrus deliciosa, three of which (nobiletin, 5-O-demethylnobiletin, and tangeritin) are bioactive. The fourth (7,4'-dihydroxy-5,6,8,3'-tetramethoxyflavone) is reported for the first time in the genus Citrus and is a potential chemotaxonomic marker. The structures of these flavones were confirmed by analysing their spectral data and comparison with similar compounds. The previously reported $^{13}C$ NMR assignment of 5-O-demethylnobiletin has been revised on the basis of 2D NMR experiments (HETCOR, COSY, and COLOC). The chemotaxonomic value of the present finding is verified.

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Synthesis and the Absolute Configurations of Isoflavanone Enantiomers

  • Won, Dong-Ho;Shin, Bok-Kyu;Han, Jae-Hong
    • Journal of Applied Biological Chemistry
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    • 제51권1호
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    • pp.17-19
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    • 2008
  • Isoflavanone has been synthesized from the reduction of isoflavone in nearly quantitative yield. Isoflavone with seven equivalents of ammonium formate in the presence of Pd/C in ethanol under $N_2$ atmosphere exclusively produced the two-electron reduced product in two hours. It was characterized by various spectroscopic methods, including UV-VIS, EI-MS, $^1H$-NMR, $^{13}C$-NMR and $^1H$, $^1H$-COSY. The racemic mixture was separated by Sumi-Chiral column chromatography and the absolute configurations of the enantiomers were characterized by circular dichroism spectroscopy.

한국 전통마을의 공간구성과 민가정원 양식 -왕곡마을을 중심으로 - (The space organization and home garden style in Korean traditional villages - the case of wang-gok villages -)

  • 윤영활;이기의;박봉우;조현길
    • 한국조경학회지
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    • 제18권2호
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    • pp.95-110
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    • 1990
  • Wang -gok Villages was forming the space marking the centripetal system from frame composed of adjacent mountains and the cosy and comfortable space perccplively and psychologically, and both the openness and closeness existed together The analysis of the circulation structure in the exterior spaces of home showed that generally one must pass through kitchen to approach to the rear yard having the strong decree of enclosure and privacy. The determinants of the space organization in Wang-gok villages and the exterior of its homes were direction and gradient as natural factor, and traditional thought, action and social class as sococultural factors. The configuration of rear garden was classified into flat type, terrace type and mixed type of natural hill and terrace. The rear garden was created purposely and actively, emphasizing the harmony with and approach to nature.

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A New Pyranoxanthone Inophyllin B from Calophyllum inophyllum

  • Ee, G.C.L.;Kua, A.S.M.;Cheow, Y.L.;Lim, C.K.;Jong, V.;Rahmani, M.
    • Natural Product Sciences
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    • 제10권5호
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    • pp.220-222
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    • 2004
  • A new prenylated pyranoxanthone, inophyllin B (1), was isolated from the roots of Calophyllum inophyllum (Guttiferae). Together with this compound was also isolated the known pyranoxanthone brasilixanthone B (2) and two common triterpenes friedelin (3) and sitosterol (4). Structural elucidations of these compounds were achieved through $^1H,\;^{13}C$, DEPT, COSY, HSQC and HMBC experiments. The molecular mass was determined using MS techniques. The crude extract indicated weak toxicity to the larvae of Aedes aegypti. We report here the isolation, structural elucidation and bioassay data for Inophyllin B and brasilixanthone B.

방선균 분리주 No. 2077이 생산하는 살충성 물질 SR 2077의 구조 동정 (Identification of inseticidal compound SR 2077 from Actinomycetes isolate No. 2077)

  • 오세량;이형규;최수근;김정일
    • Applied Biological Chemistry
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    • 제37권4호
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    • pp.234-236
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    • 1994
  • 국내 토양에서 분리한 방선균에서 살충성물질을 선발하는 연구과정 중 no. 2077 균주가 생산하는 살충성물질을 분리하였다. 살충성물질 SR2077은 UV, $^1H-NMR$, $^BC-NMR$, C-H COSY 등의 방법으로 구조분석한 결과 albocycline으로 동정되었다.

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Umbilicaria esculenta가 생산하는 Depside계 화합물의 구조 및 Phospholipase $A_2$ 저해활성 (A Phospholipase $A_2$ Inhibitor Isolated from Umilicaria esculenta)

  • 김진우;송경식;장현욱;유승헌;유익동
    • 한국미생물·생명공학회지
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    • 제23권5호
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    • pp.526-530
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    • 1995
  • Phospholipase A$_{2}$ (PLA$_{2}$) is lipolytic enzyme that has known to be involved in inflammation. In the course of our screening for antiinflammatory compounds from natural products, a compound having PLA$_{2}$ inhibitory activities was isolated from the methanol extract of Umbilicaria esculenta. The compound was identified as lecanoric acid based on various NMR studies including DEPT, HETERO-COSY and HMBC experiments. Lecanoric acid inhibited human rheumatoid synovial PLA$_{2}$ activity with IC$_{50}$ of 0.17 mM and also exhibited antitumor activity (ED$_{50}$=2.7 $\mu $g/ml) against skin tumor cell line (LOX-IMVI).

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α-Glucosidase Inhibitor Isolated from Coffee

  • Kim, Shin-Duk
    • Journal of Microbiology and Biotechnology
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    • 제25권2호
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    • pp.174-177
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    • 2015
  • A potent α-glucosidase inhibitor (compound I) was isolated from coffee brews by activity-based fractionation and identified as a β-carboline alkaloid norharman (9H-pyrido[3.4-b]indole) on the basis of mass spectroscopy and nuclear magnetic resonance spectra (1H NMR, 13C NMR, and COSY). The norharman showed potent inhibition against α-glucosidase enzyme in a concentration-dependent manner, with an IC50 value of 0.27 mM for maltase and 0.41 mM for sucrase. A Lineweaver-Burk plot revealed that norharman inhibited α-glucosidase enzyme uncompetitively, with a Ki value of 0.13 mM.

Gymnastone, A New Benzofuran Derivative from Gymnaster koraiensis

  • Dat, Nguyen-Tien;Kiem, Phan-Van;Cai, Xing-Fu;Shen, Quanghai;Bae, Ki-Hwan;Kim, Young-Ho
    • Archives of Pharmacal Research
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    • 제27권11호
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    • pp.1106-1108
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    • 2004
  • A new benzofuran derivative, named gymnastone [5-hydroxy-6-acetyl-2-(2-propane-1,2,3-triol)-benzofuran (1)], was isolated from the aerial part of Gymnaster koraiensis, together with viscidone (2) by repeated column chromatography. The structures of both compounds were identified by physico-chemical and spectral analysis including COSY, HMQC, and HMBC experiments.

A New (E)-4-Hydroxy-dodec-2-enedioic Acid from the Stem Bark of Albizzia julibrissin

  • Jung, Mee-Jung;Kang, Sam-Sik;Choi, Jae-Sue
    • Archives of Pharmacal Research
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    • 제26권3호
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    • pp.207-209
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    • 2003
  • A new unsaturated hydroxy acid was isolated from the stem bark extract of Albizzia julibrissin through repeated silica gel and Sephadex LH-20 column chromatography. The chemical structure of the new acid was determined as (E)-4-hydroxy-dodec-2-enedioic acid on the basis of several spectral data including 2D-NMR. The stereochemical feature of the double bond was determined to be E on the basis of the coupling pattern of related proton signals in the $^1H-NMR$ and COSY experiments.

Synthesis and DNA-binding Properties of Trehalose-tethered Monomeric and Dimeric Berberines

  • Wang, Yong-Min;Zhou, Chun-Qiong;Chen, Jin-Xiang;Chen, Wen-Hua
    • Bulletin of the Korean Chemical Society
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    • 제34권3호
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    • pp.749-752
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    • 2013
  • Trehalose-tethered monomeric and dimeric berberines were synthesized in 50% and 30% from the reaction of berberrubine with 6-tosyl-${\alpha}$,${\alpha}^{\prime}$-trehalose and 6,6'-ditosyl-${\alpha}$,${\alpha}^{\prime}$-trehalose, respectively, and fully characterized by MS (HR and ESI) and NMR ($^1H$, $^{13}C$, COSY and HSQC). Spectrophotometric and spectrofluorimetric titrations indicated that compared with berberine, trehalose-tethered monomeric berberine had comparable DNA-binding affinity toward calf-thymus DNA, whereas trehalose-spaced dimeric berberine exhibited higher DNA-binding affinity. The potential application of these conjugates is also briefly discussed.