Procyanidins from the stem wood of Machilus japonica and their inhibitory effect on LDL oxidation

The stem wood of Machilus japonica Siebold & Zucc were extracted with 80 % aqueous MeOH, and the concentrated extract was successively partitioned with ethyl acetate (EtOAc), normal butanol, and water. From the EtOAc fraction, five procyanidins, procyanidin A1 ( 1 ), procyanidin A2 ( 2 ), procya...

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Published inArchives of pharmacal research Vol. 37; no. 11; pp. 1403 - 1410
Main Authors Park, Hee-Jung, Kim, Su-Yeon, Song, Na-Young, Cho, Jin-Gyeong, Kang, Ji-Hyun, Jeong, Tae-Sook, Lee, Dae-Young, Kim, Geum-Soog, Kim, Yong-Bum, Kang, Hee-Cheol, Baek, Nam-In
Format Journal Article
LanguageEnglish
Published Heidelberg Pharmaceutical Society of Korea 01.11.2014
대한약학회
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ISSN0253-6269
1976-3786
1976-3786
DOI10.1007/s12272-013-0304-2

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Abstract The stem wood of Machilus japonica Siebold & Zucc were extracted with 80 % aqueous MeOH, and the concentrated extract was successively partitioned with ethyl acetate (EtOAc), normal butanol, and water. From the EtOAc fraction, five procyanidins, procyanidin A1 ( 1 ), procyanidin A2 ( 2 ), procyanidin B7 ( 3 ), cinnamtannin B1 ( 4 ), and aesculitannin B ( 5 ), were isolated. Their chemical structures were identified through spectroscopic data analyses including NMR, MS, and IR. This is the first time any of these compounds have been isolated from this plant. The compounds were evaluated for inhibition activity on LDL oxidation. All of these compounds and the positive control, BHT, showed a very high inhibition effect with IC 50 values of 0.94, 2.1, 1.8, 1.1, 1.0, and 1.9 μM, respectively.
AbstractList The stem wood of Machilus japonica Siebold & Zucc were extracted with 80 % aqueous MeOH, and the concentrated extract was successively partitioned with ethyl acetate (EtOAc), normal butanol, and water. From the EtOAc fraction, five procyanidins, procyanidin A1 ( 1 ), procyanidin A2 ( 2 ), procyanidin B7 ( 3 ), cinnamtannin B1 ( 4 ), and aesculitannin B ( 5 ), were isolated. Their chemical structures were identified through spectroscopic data analyses including NMR, MS, and IR. This is the first time any of these compounds have been isolated from this plant. The compounds were evaluated for inhibition activity on LDL oxidation. All of these compounds and the positive control, BHT, showed a very high inhibition effect with IC 50 values of 0.94, 2.1, 1.8, 1.1, 1.0, and 1.9 μM, respectively.
The stem wood of Machilus japonica Siebold & Zucc were extracted with 80 % aqueous MeOH, and the concentrated extract was successively partitioned with ethyl acetate (EtOAc), normal butanol, and water. From the EtOAc fraction, five procyanidins, procyanidin A1 (1), procyanidin A2 (2), procyanidin B7 (3), cinnamtannin B1 (4), and aesculitannin B (5), were isolated. Their chemical structures were identified through spectroscopic data analyses including NMR, MS, and IR. This is the first time any of these compounds have been isolated from this plant. The compounds were evaluated for inhibition activity on LDL oxidation. All of these compounds and the positive control, BHT, showed a very high inhibition effect with IC₅₀ values of 0.94, 2.1, 1.8, 1.1, 1.0, and 1.9 μM, respectively.
The stem wood of Machilus japonica Siebold & Zucc were extracted with 80 % aqueous MeOH, and the concentrated extract was successively partitioned with ethyl acetate (EtOAc), normal butanol, and water. From the EtOAc fraction, five procyanidins, procyanidin A1 (1), procyanidin A2 (2), procyanidin B7 (3), cinnamtannin B1 (4), and aesculitannin B (5), were isolated. Their chemical structures were identified through spectroscopic data analyses including NMR, MS, and IR. This is the first time any of these compounds have been isolated from this plant. The compounds were evaluated for inhibition activity on LDL oxidation. All of these compounds and the positive control, BHT, showed a very high inhibition effect with IC50 values of 0.94, 2.1, 1.8, 1.1, 1.0, and 1.9 μM, respectively.
The stem wood of Machilus japonica Siebold & Zucc were extracted with 80 % aqueous MeOH, and the concentrated extract was successively partitioned with ethyl acetate (EtOAc), normal butanol, and water. From the EtOAc fraction, five procyanidins, procyanidin A1 (1), procyanidin A2 (2), procyanidin B7 (3), cinnamtannin B1 (4), and aesculitannin B (5), were isolated. Their chemical structures were identified through spectroscopic data analyses including NMR, MS, and IR. This is the first time any of these compounds have been isolated from this plant. The compounds were evaluated for inhibition activity on LDL oxidation. All of these compounds and the positive control, BHT, showed a very high inhibition effect with IC50 values of 0.94, 2.1, 1.8, 1.1, 1.0, and 1.9 μM, respectively.The stem wood of Machilus japonica Siebold & Zucc were extracted with 80 % aqueous MeOH, and the concentrated extract was successively partitioned with ethyl acetate (EtOAc), normal butanol, and water. From the EtOAc fraction, five procyanidins, procyanidin A1 (1), procyanidin A2 (2), procyanidin B7 (3), cinnamtannin B1 (4), and aesculitannin B (5), were isolated. Their chemical structures were identified through spectroscopic data analyses including NMR, MS, and IR. This is the first time any of these compounds have been isolated from this plant. The compounds were evaluated for inhibition activity on LDL oxidation. All of these compounds and the positive control, BHT, showed a very high inhibition effect with IC50 values of 0.94, 2.1, 1.8, 1.1, 1.0, and 1.9 μM, respectively.
The stem wood of Machilus japonica Siebold &Zucc were extracted with 80 % aqueous MeOH, and theconcentrated extract was successively partitioned with ethylacetate (EtOAc), normal butanol, and water. From theEtOAc fraction, five procyanidins, procyanidin A1 (1),procyanidin A2 (2), procyanidin B7 (3), cinnamtannin B1(4), and aesculitannin B (5), were isolated. Their chemicalstructures were identified through spectroscopic data analysesincluding NMR, MS, and IR. This is the first time any ofthese compounds have been isolated from this plant. Thecompounds were evaluated for inhibition activity on LDLoxidation. All of these compounds and the positive control,BHT, showed a very high inhibition effect with IC50 valuesof 0.94, 2.1, 1.8, 1.1, 1.0, and 1.9 lM, respectively. KCI Citation Count: 4
Author Kim, Yong-Bum
Park, Hee-Jung
Jeong, Tae-Sook
Kim, Su-Yeon
Kang, Ji-Hyun
Lee, Dae-Young
Baek, Nam-In
Song, Na-Young
Kim, Geum-Soog
Cho, Jin-Gyeong
Kang, Hee-Cheol
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  givenname: Geum-Soog
  surname: Kim
  fullname: Kim, Geum-Soog
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– sequence: 9
  givenname: Yong-Bum
  surname: Kim
  fullname: Kim, Yong-Bum
  organization: Technology Services Division, National Institute of Horticultural and Herbal Science, RDA
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  givenname: Hee-Cheol
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Snippet The stem wood of Machilus japonica Siebold & Zucc were extracted with 80 % aqueous MeOH, and the concentrated extract was successively partitioned with ethyl...
The stem wood of Machilus japonica Siebold & Zucc were extracted with 80 % aqueous MeOH, and the concentrated extract was successively partitioned with ethyl...
The stem wood of Machilus japonica Siebold &Zucc were extracted with 80 % aqueous MeOH, and theconcentrated extract was successively partitioned with...
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SubjectTerms Antioxidants - isolation & purification
Antioxidants - pharmacology
butanol
butylated hydroxytoluene
chemical structure
ethyl acetate
inhibitory concentration 50
Lauraceae - chemistry
Lipoproteins, LDL - chemistry
low density lipoprotein
Machilus
Medicine
methanol
Molecular Structure
nuclear magnetic resonance spectroscopy
Nuclear Magnetic Resonance, Biomolecular
oxidation
Oxidation-Reduction
Pharmacology/Toxicology
Pharmacy
Plant Extracts - chemistry
Plant Stems - chemistry
Proanthocyanidins - isolation & purification
Proanthocyanidins - pharmacology
procyanidins
Research Article
stemwood
약학
Title Procyanidins from the stem wood of Machilus japonica and their inhibitory effect on LDL oxidation
URI https://link.springer.com/article/10.1007/s12272-013-0304-2
https://www.ncbi.nlm.nih.gov/pubmed/24297667
https://www.proquest.com/docview/1620024473
https://www.proquest.com/docview/1733507422
https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001927941
Volume 37
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