Triterpenoid glycosides from Ladenbergia hexandra Klotzsch
From the bark of Ladenbergia hexandra Klotzsch, ten triterpenoid glycosides were isolated along with five known compounds, and their structures were determined based on extensive NMR and mass spectroscopic, GC and HPLC analyses. Some triterpenoid glycosides contained 6-deoxy-D-allose or D-allose as...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Furukawa, Megumi [verfasserIn] |
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E-Artikel |
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Englisch |
| Erschienen: |
2017 |
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9 |
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Enthalten in: β-carotene isolated from the marine red alga, - Kavalappa, Yogendra Prasad ELSEVIER, 2018, the international journal of plant biochemistry and molecular biology : the official journal of the Phytochemical Society of Europe and the Phytochemical Society of North America, New York, NY [u.a.] |
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| Übergeordnetes Werk: |
volume:136 ; year:2017 ; pages:147-155 ; extent:9 |
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| DOI / URN: |
10.1016/j.phytochem.2017.01.014 |
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| 520 | |a From the bark of Ladenbergia hexandra Klotzsch, ten triterpenoid glycosides were isolated along with five known compounds, and their structures were determined based on extensive NMR and mass spectroscopic, GC and HPLC analyses. Some triterpenoid glycosides contained 6-deoxy-D-allose or D-allose as a sugar moiety. The absolute stereochemical assignment of the sugars was determined by comparison with synthetic samples, as well as by GC and HPLC analysis. | ||
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10.1016/j.phytochem.2017.01.014 doi GBV00000000000066A.pica (DE-627)ELV015594912 (ELSEVIER)S0031-9422(17)30034-1 DE-627 ger DE-627 rakwb eng 580 540 580 DE-600 540 DE-600 630 640 610 VZ Furukawa, Megumi verfasserin aut Triterpenoid glycosides from Ladenbergia hexandra Klotzsch 2017 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier From the bark of Ladenbergia hexandra Klotzsch, ten triterpenoid glycosides were isolated along with five known compounds, and their structures were determined based on extensive NMR and mass spectroscopic, GC and HPLC analyses. Some triterpenoid glycosides contained 6-deoxy-D-allose or D-allose as a sugar moiety. The absolute stereochemical assignment of the sugars was determined by comparison with synthetic samples, as well as by GC and HPLC analysis. Ladenbergia hexandra Elsevier Triterpene glycoside Elsevier Rubiaceae Elsevier β-D-quinovose Elsevier 6-Deoxy-β-D-allose Elsevier β-D-allose Elsevier Glycosyl iodide Elsevier Kamo, Satoshi oth Makino, Mitsuko oth Kurita, Masahiro oth Tabata, Keiichi oth Matsuzaki, Keiichi oth Suzuki, Takashi oth Uchiyama, Taketo oth Enthalten in Elsevier Science Kavalappa, Yogendra Prasad ELSEVIER β-carotene isolated from the marine red alga, 2018 the international journal of plant biochemistry and molecular biology : the official journal of the Phytochemical Society of Europe and the Phytochemical Society of North America New York, NY [u.a.] (DE-627)ELV001360140 volume:136 year:2017 pages:147-155 extent:9 https://doi.org/10.1016/j.phytochem.2017.01.014 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA AR 136 2017 147-155 9 045F 580 |
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10.1016/j.phytochem.2017.01.014 doi GBV00000000000066A.pica (DE-627)ELV015594912 (ELSEVIER)S0031-9422(17)30034-1 DE-627 ger DE-627 rakwb eng 580 540 580 DE-600 540 DE-600 630 640 610 VZ Furukawa, Megumi verfasserin aut Triterpenoid glycosides from Ladenbergia hexandra Klotzsch 2017 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier From the bark of Ladenbergia hexandra Klotzsch, ten triterpenoid glycosides were isolated along with five known compounds, and their structures were determined based on extensive NMR and mass spectroscopic, GC and HPLC analyses. Some triterpenoid glycosides contained 6-deoxy-D-allose or D-allose as a sugar moiety. The absolute stereochemical assignment of the sugars was determined by comparison with synthetic samples, as well as by GC and HPLC analysis. Ladenbergia hexandra Elsevier Triterpene glycoside Elsevier Rubiaceae Elsevier β-D-quinovose Elsevier 6-Deoxy-β-D-allose Elsevier β-D-allose Elsevier Glycosyl iodide Elsevier Kamo, Satoshi oth Makino, Mitsuko oth Kurita, Masahiro oth Tabata, Keiichi oth Matsuzaki, Keiichi oth Suzuki, Takashi oth Uchiyama, Taketo oth Enthalten in Elsevier Science Kavalappa, Yogendra Prasad ELSEVIER β-carotene isolated from the marine red alga, 2018 the international journal of plant biochemistry and molecular biology : the official journal of the Phytochemical Society of Europe and the Phytochemical Society of North America New York, NY [u.a.] (DE-627)ELV001360140 volume:136 year:2017 pages:147-155 extent:9 https://doi.org/10.1016/j.phytochem.2017.01.014 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA AR 136 2017 147-155 9 045F 580 |
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10.1016/j.phytochem.2017.01.014 doi GBV00000000000066A.pica (DE-627)ELV015594912 (ELSEVIER)S0031-9422(17)30034-1 DE-627 ger DE-627 rakwb eng 580 540 580 DE-600 540 DE-600 630 640 610 VZ Furukawa, Megumi verfasserin aut Triterpenoid glycosides from Ladenbergia hexandra Klotzsch 2017 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier From the bark of Ladenbergia hexandra Klotzsch, ten triterpenoid glycosides were isolated along with five known compounds, and their structures were determined based on extensive NMR and mass spectroscopic, GC and HPLC analyses. Some triterpenoid glycosides contained 6-deoxy-D-allose or D-allose as a sugar moiety. The absolute stereochemical assignment of the sugars was determined by comparison with synthetic samples, as well as by GC and HPLC analysis. Ladenbergia hexandra Elsevier Triterpene glycoside Elsevier Rubiaceae Elsevier β-D-quinovose Elsevier 6-Deoxy-β-D-allose Elsevier β-D-allose Elsevier Glycosyl iodide Elsevier Kamo, Satoshi oth Makino, Mitsuko oth Kurita, Masahiro oth Tabata, Keiichi oth Matsuzaki, Keiichi oth Suzuki, Takashi oth Uchiyama, Taketo oth Enthalten in Elsevier Science Kavalappa, Yogendra Prasad ELSEVIER β-carotene isolated from the marine red alga, 2018 the international journal of plant biochemistry and molecular biology : the official journal of the Phytochemical Society of Europe and the Phytochemical Society of North America New York, NY [u.a.] (DE-627)ELV001360140 volume:136 year:2017 pages:147-155 extent:9 https://doi.org/10.1016/j.phytochem.2017.01.014 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA AR 136 2017 147-155 9 045F 580 |
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10.1016/j.phytochem.2017.01.014 doi GBV00000000000066A.pica (DE-627)ELV015594912 (ELSEVIER)S0031-9422(17)30034-1 DE-627 ger DE-627 rakwb eng 580 540 580 DE-600 540 DE-600 630 640 610 VZ Furukawa, Megumi verfasserin aut Triterpenoid glycosides from Ladenbergia hexandra Klotzsch 2017 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier From the bark of Ladenbergia hexandra Klotzsch, ten triterpenoid glycosides were isolated along with five known compounds, and their structures were determined based on extensive NMR and mass spectroscopic, GC and HPLC analyses. Some triterpenoid glycosides contained 6-deoxy-D-allose or D-allose as a sugar moiety. The absolute stereochemical assignment of the sugars was determined by comparison with synthetic samples, as well as by GC and HPLC analysis. Ladenbergia hexandra Elsevier Triterpene glycoside Elsevier Rubiaceae Elsevier β-D-quinovose Elsevier 6-Deoxy-β-D-allose Elsevier β-D-allose Elsevier Glycosyl iodide Elsevier Kamo, Satoshi oth Makino, Mitsuko oth Kurita, Masahiro oth Tabata, Keiichi oth Matsuzaki, Keiichi oth Suzuki, Takashi oth Uchiyama, Taketo oth Enthalten in Elsevier Science Kavalappa, Yogendra Prasad ELSEVIER β-carotene isolated from the marine red alga, 2018 the international journal of plant biochemistry and molecular biology : the official journal of the Phytochemical Society of Europe and the Phytochemical Society of North America New York, NY [u.a.] (DE-627)ELV001360140 volume:136 year:2017 pages:147-155 extent:9 https://doi.org/10.1016/j.phytochem.2017.01.014 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA AR 136 2017 147-155 9 045F 580 |
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10.1016/j.phytochem.2017.01.014 doi GBV00000000000066A.pica (DE-627)ELV015594912 (ELSEVIER)S0031-9422(17)30034-1 DE-627 ger DE-627 rakwb eng 580 540 580 DE-600 540 DE-600 630 640 610 VZ Furukawa, Megumi verfasserin aut Triterpenoid glycosides from Ladenbergia hexandra Klotzsch 2017 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier From the bark of Ladenbergia hexandra Klotzsch, ten triterpenoid glycosides were isolated along with five known compounds, and their structures were determined based on extensive NMR and mass spectroscopic, GC and HPLC analyses. Some triterpenoid glycosides contained 6-deoxy-D-allose or D-allose as a sugar moiety. The absolute stereochemical assignment of the sugars was determined by comparison with synthetic samples, as well as by GC and HPLC analysis. Ladenbergia hexandra Elsevier Triterpene glycoside Elsevier Rubiaceae Elsevier β-D-quinovose Elsevier 6-Deoxy-β-D-allose Elsevier β-D-allose Elsevier Glycosyl iodide Elsevier Kamo, Satoshi oth Makino, Mitsuko oth Kurita, Masahiro oth Tabata, Keiichi oth Matsuzaki, Keiichi oth Suzuki, Takashi oth Uchiyama, Taketo oth Enthalten in Elsevier Science Kavalappa, Yogendra Prasad ELSEVIER β-carotene isolated from the marine red alga, 2018 the international journal of plant biochemistry and molecular biology : the official journal of the Phytochemical Society of Europe and the Phytochemical Society of North America New York, NY [u.a.] (DE-627)ELV001360140 volume:136 year:2017 pages:147-155 extent:9 https://doi.org/10.1016/j.phytochem.2017.01.014 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA AR 136 2017 147-155 9 045F 580 |
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Furukawa, Megumi |
| doi_str_mv |
10.1016/j.phytochem.2017.01.014 |
| dewey-full |
580 540 630 640 610 |
| title_sort |
triterpenoid glycosides from ladenbergia hexandra klotzsch |
| title_auth |
Triterpenoid glycosides from Ladenbergia hexandra Klotzsch |
| abstract |
From the bark of Ladenbergia hexandra Klotzsch, ten triterpenoid glycosides were isolated along with five known compounds, and their structures were determined based on extensive NMR and mass spectroscopic, GC and HPLC analyses. Some triterpenoid glycosides contained 6-deoxy-D-allose or D-allose as a sugar moiety. The absolute stereochemical assignment of the sugars was determined by comparison with synthetic samples, as well as by GC and HPLC analysis. |
| abstractGer |
From the bark of Ladenbergia hexandra Klotzsch, ten triterpenoid glycosides were isolated along with five known compounds, and their structures were determined based on extensive NMR and mass spectroscopic, GC and HPLC analyses. Some triterpenoid glycosides contained 6-deoxy-D-allose or D-allose as a sugar moiety. The absolute stereochemical assignment of the sugars was determined by comparison with synthetic samples, as well as by GC and HPLC analysis. |
| abstract_unstemmed |
From the bark of Ladenbergia hexandra Klotzsch, ten triterpenoid glycosides were isolated along with five known compounds, and their structures were determined based on extensive NMR and mass spectroscopic, GC and HPLC analyses. Some triterpenoid glycosides contained 6-deoxy-D-allose or D-allose as a sugar moiety. The absolute stereochemical assignment of the sugars was determined by comparison with synthetic samples, as well as by GC and HPLC analysis. |
| collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA |
| title_short |
Triterpenoid glycosides from Ladenbergia hexandra Klotzsch |
| url |
https://doi.org/10.1016/j.phytochem.2017.01.014 |
| remote_bool |
true |
| author2 |
Kamo, Satoshi Makino, Mitsuko Kurita, Masahiro Tabata, Keiichi Matsuzaki, Keiichi Suzuki, Takashi Uchiyama, Taketo |
| author2Str |
Kamo, Satoshi Makino, Mitsuko Kurita, Masahiro Tabata, Keiichi Matsuzaki, Keiichi Suzuki, Takashi Uchiyama, Taketo |
| ppnlink |
ELV001360140 |
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false |
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| author2_role |
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| doi_str |
10.1016/j.phytochem.2017.01.014 |
| up_date |
2024-07-06T18:07:34.241Z |
| _version_ |
1803854025056059392 |
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|
| score |
7.399913 |