• 제목/요약/키워드: HMBC

검색결과 158건 처리시간 0.02초

한국산 해양 의충동물 개불에서 Anthraquinone 및 Sterol 성분연구 (Anthraquinones and Sterols from the Korean Marine Echiura Urechis unicintus)

  • 장성근;박영현;채석;김인규;서영완;조기웅;신종헌
    • 대한화학회지
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    • 제42권1호
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    • pp.64-68
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    • 1998
  • 한국 연해에 서식하고 있는 의충동물 개불(Urechis unicintus)로 부터 강심작용과 관련된 $Na^+,K^+-ATPase$ 저해 작용 및 cyclic AMP phosphodiesterase 저해 작용이 높은 anthraquinones화합물인 chrysophanol, physcion 및 1-o-methyl-2methoxychrysophanol을 분리하였다.주로 HMQC, HMBC 및 NOE 등의 분광학적 방법으로 이들의 구조를 밝혔다.

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산호로부터 2개의 푸란노세스키테르펜의 분리와 구조 결정 (Isolation and Structure Determination of Two Furanosesquiterpenes from the Soft Coral Sinularia lochmodes)

  • 박선구
    • 대한화학회지
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    • 제38권10호
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    • pp.749-752
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    • 1994
  • 하와이 Pohnpei에서 채집한 soft coral Sinularia lochmodes로부터 2개의 furanosesquiterpenes인 (5'E)-5-(2',6'-dimethylocta-5',7'-dienyl) furan-3-carboxylic acid (1)와 (1'E,5'E)-5-(2',6'-dimethylocta-l',5',7'-trienyl) furan-3-carboxylic acid (2)가 검출되었다. 이들의 구조를 $^1H$ , $^{13}C$ NMR, Homo-COSY, $^1H$-$^{13}C$ (1 bond) Heteronuclear Multiple Quantum Coherence Spectroscopy (HMQC), $^1H$-$^{13}C$ (2 and 3 bond) Heteronuclear Multiple Bond Coherence Spectroscopy (HMBC), Electron Impact Mass Spectroscopy (EI-ms) 및 Infrared Spectroscopy (IR)에 의해 밝혔다.

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염생식물 갯방풍의 화학적 성분연구 (Chemical Constituents of the Halophyte Glehnia littoralis)

  • 엄영란;이정임;이진혁;김해진;예성수;서영완
    • 대한화학회지
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    • 제54권6호
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    • pp.701-706
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    • 2010
  • 우리나라 동해안에 서식하는 염생식물인 갯방풍으로부터 2개의 polyacetylene 화합물인 falcarindiol(1)과 falcarinol(2), 4개의 coumarin 화합물인 bergapten(3), xanthotoxin(4), umbelliferone(5), scopoletin(6) 및 1개의 sesquiterpene 화합물인 $(5\beta,10\alpha)$-lasidiol angelate(7)가 분리되었다. 이들 화합물 중 scopoletin(6)과 $(5\beta,10\alpha)$-Lasidiol angelate(7)는 갯방풍으로부터 처음 분리되어진 것이다. 분리된 화합물의 구조결정은 $^1H$ COSY, HMQC 그리고 HMBC와 같은 2D NMR 분광학적 실험과 문헌에 보고 된 값을 비교하여 이루어졌다.

참느릅나무의 성분에 관한 연구 (Studies on the Constituents of Ulmus parvifolia)

  • 문영희;임기룡
    • 생약학회지
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    • 제26권1호
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    • pp.1-7
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    • 1995
  • The bark of Ulmus parvifolia Jacq. (Ulmaceae) has been used for the treatment of gonorhea, edema, scabies and eczema marginatum. Previous investigations conducted with the heartwood and leaves have demonstrated it to contain sesquiterpenes as well as fat acids from the heartwood and flavonol glycosides from leaves. However, no phytochemical work has been done on the bark parts of this plant. Investigation of the phytochemical constituents in the barks of U. parvifolia has resulted in the isolation of sterols, sterol glucoside and a catechin glycoside, $(+)-catechin\;7-O-{\alpha}-{_L}-rhamnopyranoside$, all of which were isolated for the first time from this plant. Sterols were consisted of the three components, ${\beta}-sitosterol$, stigmasterol and campesterol in a ratio of 92.1:4.1:3.8, and sterol glucoside was identified as ${\beta}-sitosterol\;3-O-{\beta}-{_D}-glucoside$. The structure of the catechin $7-O-{\alpha}-{_L}-rhamnoside$ was established primarily by analysis of $^1H-and$ COSY-45 NMR, HMQC and HMBC and EI mass spectra of the heptaacetate. Especially, HMBC spectrum provides effective way for the determination of the point of attachment of the rhamnosyl group to catechin moiety.

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Wewakamide A and Guineamide G, Cyclic Depsipeptides from the Marine Cyanobacteria Lyngbya semiplena and Lyngbya majuscula

  • Han, Bingnan;Gross, Harald;Mcphail, Kerry L.;Goeger, Doug;Maier, Claudia S.;Gerwick, William H.
    • Journal of Microbiology and Biotechnology
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    • 제21권9호
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    • pp.930-936
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    • 2011
  • Two new cyclic depsipeptides wewakamide A (1) and guineamide G (2) have been isolated from the marine cyanobacterium Lyngbya semiplena and Lyngbya majuscula, respectively, collected from Papua New Guinea. The amino and hydroxy acid partial structures of wewakamide A and guineamide G were elucidated through extensive spectroscopic techniques, including HR-FABMS, 1D $^1H$ and $^{13}C$ NMR, as well as 2D COSY, HSQC, HSQC-TOCSY, and HMBC spectra. The sequence of the residues of wewakamide A was determined through a combination of ESI-MS/MS, HMBC, and ROESY. Wewakamide A possesses a ${\beta}$-amino acid, 3-amino-2-methylbutanoic acid (Maba) residue, which has only been previously identified in two natural products, guineamide B (3) and dolastatin D (4). Although both new compounds (1,2) showed potent brine shrimp toxicity, only guineamide G displayed significant cytotoxicity to a mouse neuroblastoma cell line with $LC_{50}$ values of 2.7 ${\mu}M$.

Constituents of the Herb of Isodon excisus var. coreanus

  • Kim, Ho-Kyoung;Whang, Wan-Kyunn;Kim, Il-Hyuk
    • Archives of Pharmacal Research
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    • 제20권3호
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    • pp.291-296
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    • 1997
  • The studies were carried out to evaluate the constituents in the aerial part of Isodon excisus var. coreanus (Labiatae). From the aqueous fraction of methanol extract, compound I (${\alpha}$-[[3-(3, 4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-3,4-dihydroxy-benzenepropanoic acid), compound II (9-methyl-dihydroferulic acid-4-O-.betha.-D-glucopyranosyl $(1{\rightarrow}2)$-${\alpha}$-L- rhamnopyranosyl (1.rarw.4)-.betha.-D-glucopyranoside), compound III (ent-7.alpha., 11${\alpha}$,15.betha.-trihydroxy-kaur-16-en-1-O-.betha.-D-glucopyranoside) and compound IV ($2{\alpha}$,3${\beta}$,$7{\alpha}$,23-tetrahydroxy-olean-12 -en-28-oic acid 28-O-${\beta}$-D-glucopyranoside) were isolated and identified on the basis of their physicochemical and spectroscopic evidences[IR, FAB(-)MS,$^{1}H-NMR,$$^{13}C-NMR,$$ HMQC$$^{1}H-^{1}H $COSY and HMBC (Heteronuclear Multiple Bond Connectivity)]. Especially, New compounds II and III were named Isodonin A and Isodonin B respectively.

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쇠비름에서 분리된 2개의 Biophenolic Glycosides (Two Biophenolic Glycosides from Portulaca oleracea)

  • 서영완;신종헌;이범종;이동석
    • 대한화학회지
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    • 제47권1호
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    • pp.43-46
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    • 2003
  • 우리나라에 널리 분포하며 오래 동안 약용으로 사용되어 온 쇠비름으로부터 페놀 글리코시드인 3-hydroxy-1(2-hydroxyethyl)phenyl-4-O-${\beta}$-D-glucopyranoside(1)과 2-(3,4-dihydroxyphenyl)ethyl-O-${\beta}$-D-glucopyranoside (2)를 칼럼 크로마토그래피 및 역상 HPLC로 분리하였으며, NOESY, HMQC, HMBC와 같은 이차원적인 NMR 분광실험에 의해서 이 물질들의 $^{13}C$ NMR 분광 데이터 값의 지정이 수정되었다. DPPH를 이용하여 이 물질들의 항산화 활성을 측정한 결과 주목할 만한 활성을 나타내었다.

다제내성 Staphylococcus aureus에 항균활성을 나타내는 CNU30122 균주가 생산하는 항생물질 (An Antibiotic against Multidrug-resistant Staphylococcus aureus Produced by Strain CNU30122)

  • 윤봉식;조수묵;김창진;유익동
    • Applied Biological Chemistry
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    • 제38권6호
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    • pp.577-580
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    • 1995
  • 다제내성 Staphylococcus aureus균주에 강력한 항균활성을 나타내는 CNU30122 균주를 선발하였다. 선발된 CNU30122균주의 배양액 추출물로부터 Diaion HP-20 column chromatograpy, ethylacetate 추출, silica gel 및 Sephadex LH-20 column chromatography, HPLC 등에 의해 백색분말의 순수한 화합물을 분리정제 하였다. 본 물질의 구조분석을 위하여 $^1H$$^{13}C\;NMR,\;DEPT,\;^1H-^1H\;COSY,\;^1H-^{13}C\;COSY$ 및 HMBC spectrum을 분석한 결과 본 물질은 분자량 516, 분자식 $C_{31}H_{48}O_6$의 tetracyclic triterpenoic acid 계열인 fusidic acid로 동정 되었다. 본화합물은 streptomycin, pecicillin, kanamycin, tetracycline 등의 약제에 내성균주인 Staphylococcus aureus R209 균주에 선택적으로 강한 항균활성을 나타내었다.

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The synthesis and the structural analysis of advanced PVC plasticizer, 2,2,4-trimethyl-1,3-pentanediol-1-butyrate-3-isobutyrate

  • Cho Myo-Kyung;Ko Dong-Hyun;Lim Young-Hee;Jung Min-Hwan;Cho Hye-Sung;Ok Jong-Hoa
    • 한국자기공명학회논문지
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    • 제9권2호
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    • pp.103-109
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    • 2005
  • New PVC plasticizer, 2,2,4-trimethyl-1,3-pentanediol-1-butyrate-3-isobutyrate was synthesized via simple esterification with butyric acid and Texanol(a trademark of Eastman Chemicals), the mixture of 2,2,4-trimethyl-1,3-pentanediol-3-isobutyrate and 2,2,4-trimethyl-1,3-pentanediol-1-isobutyrate. The analysis of $^1H-1D,\;^{13}C-1D$ NMR and HMBC spectra identified internal-ester-transfer of 2,2,4-trimethyl-1,3-pentanediol-1-isobutyrate during the reaction. 2,2,4-trimethyl-1,3-pentanediol-1-butyrate-3-isobutyrate gave better properties in PVC than 2,2,4-trimethyl-1,3-pentanediol diisobutyrate(TXIB, a trademark of Eastman Chemicals) such as lower viscosity, higher tensile strength and better elongation. In particular, remarkably reduced migration compared with TXIB suggested a reduced emission of VOC(volatile organic compound) from PVC.

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당느릅나무로부터 Sesquiterpene o-Naphthoquinone류 화합물, Mansonone E, F 및 H의 분리와 구조결정 (Isolation and Identification of Sesquiterpene o-Naphthoquinones, Mansonones E, F and H, from the Root Bark of Ulmus davidiana Planch)

  • 김종평;김원곤;;박종희;정진;유익동
    • Applied Biological Chemistry
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    • 제39권1호
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    • pp.89-94
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    • 1996
  • 한방에서 종기, 치질, 위암 및 염증의 치료목적으로 사용되어온 당느릅나무 (Ulmus davidiana Planch) 근피의 메탄을 추출물로부터 sesquiterpene o-naphthoquinone류 화합물 세가지를 분리 정제하였다. 이들의 구조를 UV-vis, IR, EIMS, HR-EIMS 및 여러 가지 NMR 스펙트럼, 특히 새로운 기법인 pulse field gradient (PFG)-HMQC 및 HMBC 스펙트럼의 분석에 의하여 결정하였다. 그 결과 이들은 2,3-dihydro-3,6,9-trimethylnaphtho(1,8-b,c)pyran-7,8-dione, 3,6,9-trimethylnaphtho(1,8-b,c)pyran-7,8-dione 및 2,3-dihydro-4-hydroxy-3,6,9-trimethylnaphtho(1,8-b,c)pyran-7,8-dione으로 동정 되었으며, 각각 mansonone E, F 및 H로 밝혀졌다. 이 화합물들은 당느릅나무에서는 처음 분리되었으며, 특히 mansonone H는 아프리카 열대식물인 Mansonia altissima Chev 및 Helicters angustifolia에서 분리된 후 자연계에서 처음으로 분리되었다. 문헌에 잘못 보고된 mansonone E 와 F의 C-3a, C-6a 및 C-9b의 세 사급탄소의 chemical shift를 최신 PFG-NMR기법에 의하여 동정하여 교정하였다.

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