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 in | Archives of pharmacal research Vol. 37; no. 11; pp. 1403 - 1410 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Heidelberg
Pharmaceutical Society of Korea
01.11.2014
대한약학회 |
Subjects | |
Online Access | Get full text |
ISSN | 0253-6269 1976-3786 1976-3786 |
DOI | 10.1007/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 |
Author_xml | – sequence: 1 givenname: Hee-Jung surname: Park fullname: Park, Hee-Jung organization: Oriental Medicinal Materials & Processing, Graduate School of Biotechnology, Kyung Hee University – sequence: 2 givenname: Su-Yeon surname: Kim fullname: Kim, Su-Yeon organization: Oriental Medicinal Materials & Processing, Graduate School of Biotechnology, Kyung Hee University – sequence: 3 givenname: Na-Young surname: Song fullname: Song, Na-Young organization: Oriental Medicinal Materials & Processing, Graduate School of Biotechnology, Kyung Hee University – sequence: 4 givenname: Jin-Gyeong surname: Cho fullname: Cho, Jin-Gyeong organization: Oriental Medicinal Materials & Processing, Graduate School of Biotechnology, Kyung Hee University – sequence: 5 givenname: Ji-Hyun surname: Kang fullname: Kang, Ji-Hyun organization: National Research Laboratory of Lipid Metabolism and Atherosclerosis, Korea Research Institute of Bioscience and Biotechnology – sequence: 6 givenname: Tae-Sook surname: Jeong fullname: Jeong, Tae-Sook organization: National Research Laboratory of Lipid Metabolism and Atherosclerosis, Korea Research Institute of Bioscience and Biotechnology – sequence: 7 givenname: Dae-Young surname: Lee fullname: Lee, Dae-Young organization: Department of Herbal Crop Research, National Institute of Horticultural and Herbal Science, RDA – sequence: 8 givenname: Geum-Soog surname: Kim fullname: Kim, Geum-Soog organization: Department of Herbal Crop Research, National Institute of Horticultural and Herbal Science, RDA – sequence: 9 givenname: Yong-Bum surname: Kim fullname: Kim, Yong-Bum organization: Technology Services Division, National Institute of Horticultural and Herbal Science, RDA – sequence: 10 givenname: Hee-Cheol surname: Kang fullname: Kang, Hee-Cheol organization: R&D Center, GFC Co., Ltd – sequence: 11 givenname: Nam-In surname: Baek fullname: Baek, Nam-In email: nibaek@khu.ac.kr organization: Oriental Medicinal Materials & Processing, Graduate School of Biotechnology, Kyung Hee University |
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CitedBy_id | crossref_primary_10_1007_s11101_021_09773_1 crossref_primary_10_1016_j_jep_2020_112548 crossref_primary_10_3390_molecules30010111 crossref_primary_10_1002_cbdv_202100807 crossref_primary_10_1515_hf_2018_0267 |
Cites_doi | 10.1021/jf0300184 10.1021/jf9810517 10.1021/jf9709156 10.1021/jf000363i 10.1016/S0031-9422(00)90571-5 10.1016/S0005-2760(96)00154-3 10.1271/bbb.110085 10.1016/S0024-3205(00)00771-2 10.5053/ejobios.2010.4.0.6 10.1248/cpb.49.551 10.1016/j.chroma.2007.11.028 10.1021/jf050418m 10.1016/j.bmc.2004.06.001 10.1021/np9000653 10.1046/j.1523-1747.1999.00532.x 10.1016/j.foodchem.2007.05.022 10.1246/bcsj.49.3564 10.1046/j.1600-0749.2003.00093.x 10.1016/S0031-9422(98)00736-5 |
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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 |
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