(Q104920105)

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981280-7

1 reference

(3S)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

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(3S)-3-(2,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-2,3-dihydropyrano[2,3-h]chromen-4-one

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3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-8-(4-hydroxy-3-methylbut-2-enyl)chromen-4-one

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(6aS,11aR)-2,10-bis(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a,9-triol

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(6aS,11aS)-4,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol

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(3S)-3-(2,4-dihydroxyphenyl)-7-hydroxy-8-[(E)-4-hydroxy-3-methylbut-2-enyl]-2,3-dihydrochromen-4-one

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(6aS,11aR)-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol

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2',4',5,7,8-Pentahydroxyisoflavone

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(3S)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(E)-4-hydroxy-3-methylbut-2-enyl]-2,3-dihydrochromen-4-one

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5,7,2',4'-Tetrahydroxy-8,3'-di(gamma,gamma-dimethylallyl)-isoflavanone

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(6aS,11aS)-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol

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(3S)-5,7-dihydroxy-3-(4-hydroxy-2-methoxyphenyl)-2,3-dihydrochromen-4-one

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(3S)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-(3-hydroxy-3-methylbutyl)-2,3-dihydrochromen-4-one

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(9R)-3-(2,4-dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one

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(3S)-3-(2,4-dihydroxyphenyl)-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

1 reference

(3S)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-(4-hydroxy-3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

1 reference

(3R,9S)-3-(2,4-dihydroxyphenyl)-5,9-dihydroxy-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one

1 reference

1 reference

2',4',7-trihydroxyisoflavone

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3-(2,4-dihydroxyphenyl)-7,8-dihydroxychromen-4-one

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(8S)-3-(2,4-dihydroxyphenyl)-5-hydroxy-8-(2-hydroxypropan-2-yl)-8,9-dihydrofuro[2,3-h]chromen-4-one

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(3R)-3-(2,4-dihydroxyphenyl)-7-hydroxy-8-[(E)-4-hydroxy-3-methylbut-2-enyl]-2,3-dihydrochromen-4-one

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Melanie J. O'Neill

1

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981280-7

S.A. Adesanya

series ordinal

2

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981280-7

Margaret F. Roberts

series ordinal

3

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981280-7

Inez R. Pantry

series ordinal

4

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981280-7

publication date

May 1986

3 references

16 September 2022

16 September 2022

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981280-7

volume

25

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981280-7

page(s)

1315-1322

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981280-7

issue

6

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981280-7

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Antifungal Phytoalexins in Phaseolus aureus Roxb

1 reference

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7 January 2021

Induced and Constitutive Isoflavonoids in Phaseolus mungo L. Leguminosae

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2981280-7

7 January 2021

Isoflavonoids from Phaseolus coccineus

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2981280-7

7 January 2021

Susceptibility of zoopathogenic fungi to phytoalexins

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2981280-7

7 January 2021

New isoflavonoids related to kievitone from Phaseolus vulgaris

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2981280-7

7 January 2021

Post-Infectional Compounds From the French Bean Phaseolus vulgaris; Isolation and Identification of Genistein and 2',4',5,7-Tetrahydroxyisoflavone

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2981280-7

7 January 2021

Biosynthesis of Isoflavonoid Phytoalexins: Incorporation of Sodium [1,2-13C2] Acetate into Phaseollin and Kievitone

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2981280-7

7 January 2021

Phaseollin formation and metabolism in Phaseolus vulgaris

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2981280-7

7 January 2021

Biosynthesis of the phytoalexin phaseollin in Phaseolus vulgaris

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2981280-7

7 January 2021

A New Isoflavone with Antifungal Activity from Immature Fruits of Lupinus luteus

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2981280-7

7 January 2021

Antimicrobial Agents from an East African Medicinal Plant Erythrina abyssinica

1 reference

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7 January 2021