Two New Antifungal Naphthoxirene Derivatives and their Glucosides from Sesamum angolense WELW
Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were...
Ausführliche Beschreibung
Gespeichert in:
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| Format: |
E-Artikel |
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| Sprache: |
Deutsch |
| Erschienen: |
1987 |
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| Umfang: |
1 Ill. ; 2 Tab. 7 |
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| Reproduktion: |
Wiley InterScience Backfile Collection 1832-2000 |
|---|---|
| Übergeordnetes Werk: |
in: Helvetica Chimica Acta - New York, NY : Wiley-VCH, 70(1987) vom: Juni, Seite 1551-1557 |
| Übergeordnetes Werk: |
volume:70 ; year:1987 ; month:06 ; pages:1551-1557 ; extent:7 |
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| 520 | |a Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were deduced by spectroscopic (IR, UV, 1H-NMR, 13C-NMR, EI-MS, DCI-MS) and chemical methods (oxidation, acid and enzymatic hydrolysis). Compounds 1-3 exhibited antifungal activity. Naphthoxirene 1 was, in addition, cytotoxic to human colon carcinoma cells. | ||
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(DE-627)NLEJ162659059 DE-627 ger DE-627 rakwb ger Two New Antifungal Naphthoxirene Derivatives and their Glucosides from Sesamum angolense WELW 1987 1 Ill. 2 Tab. 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were deduced by spectroscopic (IR, UV, 1H-NMR, 13C-NMR, EI-MS, DCI-MS) and chemical methods (oxidation, acid and enzymatic hydrolysis). Compounds 1-3 exhibited antifungal activity. Naphthoxirene 1 was, in addition, cytotoxic to human colon carcinoma cells. Wiley InterScience Backfile Collection 1832-2000 Potterat, Olivier oth Stoeckli-Evans, Helen oth Msonthi, Jerome D. oth Hostettmann, Kurt oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 70(1987) vom: Juni, Seite 1551-1557 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:70 year:1987 month:06 pages:1551-1557 extent:7 http://dx.doi.org/10.1002/hlca.19870700613 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 70 1987 6 1551-1557 7 |
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(DE-627)NLEJ162659059 DE-627 ger DE-627 rakwb ger Two New Antifungal Naphthoxirene Derivatives and their Glucosides from Sesamum angolense WELW 1987 1 Ill. 2 Tab. 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were deduced by spectroscopic (IR, UV, 1H-NMR, 13C-NMR, EI-MS, DCI-MS) and chemical methods (oxidation, acid and enzymatic hydrolysis). Compounds 1-3 exhibited antifungal activity. Naphthoxirene 1 was, in addition, cytotoxic to human colon carcinoma cells. Wiley InterScience Backfile Collection 1832-2000 Potterat, Olivier oth Stoeckli-Evans, Helen oth Msonthi, Jerome D. oth Hostettmann, Kurt oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 70(1987) vom: Juni, Seite 1551-1557 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:70 year:1987 month:06 pages:1551-1557 extent:7 http://dx.doi.org/10.1002/hlca.19870700613 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 70 1987 6 1551-1557 7 |
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(DE-627)NLEJ162659059 DE-627 ger DE-627 rakwb ger Two New Antifungal Naphthoxirene Derivatives and their Glucosides from Sesamum angolense WELW 1987 1 Ill. 2 Tab. 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were deduced by spectroscopic (IR, UV, 1H-NMR, 13C-NMR, EI-MS, DCI-MS) and chemical methods (oxidation, acid and enzymatic hydrolysis). Compounds 1-3 exhibited antifungal activity. Naphthoxirene 1 was, in addition, cytotoxic to human colon carcinoma cells. Wiley InterScience Backfile Collection 1832-2000 Potterat, Olivier oth Stoeckli-Evans, Helen oth Msonthi, Jerome D. oth Hostettmann, Kurt oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 70(1987) vom: Juni, Seite 1551-1557 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:70 year:1987 month:06 pages:1551-1557 extent:7 http://dx.doi.org/10.1002/hlca.19870700613 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 70 1987 6 1551-1557 7 |
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(DE-627)NLEJ162659059 DE-627 ger DE-627 rakwb ger Two New Antifungal Naphthoxirene Derivatives and their Glucosides from Sesamum angolense WELW 1987 1 Ill. 2 Tab. 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were deduced by spectroscopic (IR, UV, 1H-NMR, 13C-NMR, EI-MS, DCI-MS) and chemical methods (oxidation, acid and enzymatic hydrolysis). Compounds 1-3 exhibited antifungal activity. Naphthoxirene 1 was, in addition, cytotoxic to human colon carcinoma cells. Wiley InterScience Backfile Collection 1832-2000 Potterat, Olivier oth Stoeckli-Evans, Helen oth Msonthi, Jerome D. oth Hostettmann, Kurt oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 70(1987) vom: Juni, Seite 1551-1557 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:70 year:1987 month:06 pages:1551-1557 extent:7 http://dx.doi.org/10.1002/hlca.19870700613 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 70 1987 6 1551-1557 7 |
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(DE-627)NLEJ162659059 DE-627 ger DE-627 rakwb ger Two New Antifungal Naphthoxirene Derivatives and their Glucosides from Sesamum angolense WELW 1987 1 Ill. 2 Tab. 7 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were deduced by spectroscopic (IR, UV, 1H-NMR, 13C-NMR, EI-MS, DCI-MS) and chemical methods (oxidation, acid and enzymatic hydrolysis). Compounds 1-3 exhibited antifungal activity. Naphthoxirene 1 was, in addition, cytotoxic to human colon carcinoma cells. Wiley InterScience Backfile Collection 1832-2000 Potterat, Olivier oth Stoeckli-Evans, Helen oth Msonthi, Jerome D. oth Hostettmann, Kurt oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 70(1987) vom: Juni, Seite 1551-1557 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:70 year:1987 month:06 pages:1551-1557 extent:7 http://dx.doi.org/10.1002/hlca.19870700613 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 70 1987 6 1551-1557 7 |
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Two New Antifungal Naphthoxirene Derivatives and their Glucosides from Sesamum angolense WELW |
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Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were deduced by spectroscopic (IR, UV, 1H-NMR, 13C-NMR, EI-MS, DCI-MS) and chemical methods (oxidation, acid and enzymatic hydrolysis). Compounds 1-3 exhibited antifungal activity. Naphthoxirene 1 was, in addition, cytotoxic to human colon carcinoma cells. |
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Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were deduced by spectroscopic (IR, UV, 1H-NMR, 13C-NMR, EI-MS, DCI-MS) and chemical methods (oxidation, acid and enzymatic hydrolysis). Compounds 1-3 exhibited antifungal activity. Naphthoxirene 1 was, in addition, cytotoxic to human colon carcinoma cells. |
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Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were deduced by spectroscopic (IR, UV, 1H-NMR, 13C-NMR, EI-MS, DCI-MS) and chemical methods (oxidation, acid and enzymatic hydrolysis). Compounds 1-3 exhibited antifungal activity. Naphthoxirene 1 was, in addition, cytotoxic to human colon carcinoma cells. |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ162659059</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210707094651.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070201s1987 xx |||||o 00| ||ger c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ162659059</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">ger</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Two New Antifungal Naphthoxirene Derivatives and their Glucosides from Sesamum angolense WELW</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1987</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="b">1 Ill.</subfield><subfield code="b">2 Tab.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">7</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Two novel naphthoxirene derivatives 1 and 2 their glucosides 3 and 4 have been isolated from the root bark of Sesamum angolense Welw. (Pedaliaceae) by preparative liquid chromatography. The structure of 1 was established by X-ray diffraction analysis. The identities of the other naphthcxirenes were deduced by spectroscopic (IR, UV, 1H-NMR, 13C-NMR, EI-MS, DCI-MS) and chemical methods (oxidation, acid and enzymatic hydrolysis). Compounds 1-3 exhibited antifungal activity. Naphthoxirene 1 was, in addition, cytotoxic to human colon carcinoma cells.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Wiley InterScience Backfile Collection 1832-2000</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Potterat, Olivier</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Stoeckli-Evans, Helen</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Msonthi, Jerome D.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hostettmann, Kurt</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Helvetica Chimica Acta</subfield><subfield code="d">New York, NY : Wiley-VCH</subfield><subfield code="g">70(1987) vom: Juni, Seite 1551-1557</subfield><subfield code="w">(DE-627)NLEJ159071178</subfield><subfield code="w">(DE-600)1475013-2</subfield><subfield code="x">0018-019X</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:70</subfield><subfield code="g">year:1987</subfield><subfield code="g">month:06</subfield><subfield code="g">pages:1551-1557</subfield><subfield code="g">extent:7</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1002/hlca.19870700613</subfield><subfield code="q">text/html</subfield><subfield code="z">Deutschlandweit zugänglich</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-WIS</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">70</subfield><subfield code="j">1987</subfield><subfield code="c">6</subfield><subfield code="h">1551-1557</subfield><subfield code="g">7</subfield></datafield></record></collection>
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7.401991 |