Diverse oxygenated isoflavonoids from Piscidia erythrina (Q104396667)

5,7-dihydroxy-3-[(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-methoxy-2,3-dihydro-1-benzofuran-7-yl]chromen-4-one

1 reference

5,7-dihydroxy-3-[(3S)-3-hydroxy-5,6-dimethoxy-2,2-dimethyl-3,4-dihydrochromen-8-yl]chromen-4-one

1 reference

3-[(3R)-3,5-dihydroxy-6-methoxy-2,2-dimethyl-3,4-dihydrochromen-8-yl]-5,7-dihydroxychromen-4-one

1 reference

5,7-dihydroxy-3-[(2S)-2-(2-hydroxypropan-2-yl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]chromen-4-one

1 reference

5,7-dihydroxy-3-[(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-methoxy-2,3-dihydro-1-benzofuran-7-yl]chromen-4-one

1 reference

5,7-dihydroxy-3-[(2R)-2-(2-hydroxypropan-2-yl)-4,5-dimethoxy-2,3-dihydro-1-benzofuran-7-yl]chromen-4-one

1 reference

trans-Hydroxypiscerythrone

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1 reference

7-Hydroxy-3-(8-hydroxy-7-methoxy-2,2-dimethylchromen-5-yl)chromen-4-one

1 reference

5,7-dihydroxy-3-[(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]chromen-4-one

1 reference

3-{2,4-dihydroxy-3-[(2E)-4-hydroxy-3-methylbut-2-en-1-yl]-5-methoxyphenyl}-5,7-dihydroxychromen-4-one

1 reference

5,7-dihydroxy-3-[(3R)-3-hydroxy-5,6-dimethoxy-2,2-dimethyl-3,4-dihydrochromen-8-yl]chromen-4-one

1 reference

3-[(3S)-3,5-dihydroxy-8-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-5,7-dihydroxychromen-4-one

1 reference

3-[2,4-Dihydroxy-3-(3-hydroxy-3-methylbutyl)-5-methoxyphenyl]-5,7-dihydroxychromen-4-one

1 reference

5,7-Dihydroxy-3-[2-hydroxy-3-(3-hydroxy-3-methylbutyl)-4,5-dimethoxyphenyl]chromen-4-one

1 reference

3-[2,4-Dihydroxy-3-(4-hydroxy-3-methylbut-2-enyl)-5-methoxyphenyl]-5,7-dihydroxychromen-4-one

1 reference

3-[(3S)-3,8-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydrochromen-5-yl]-5,7-dihydroxychromen-4-one

1 reference

1 reference

5,7-dihydroxy-3-[(2R)-2-(2-hydroxypropan-2-yl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]chromen-4-one

1 reference

3-[(3R)-3,8-dihydroxy-7-methoxy-2,2-dimethyl-6-(3-methylbut-2-enyl)-3,4-dihydrochromen-5-yl]-5,7-dihydroxychromen-4-one

1 reference

1 reference

1 reference

7-Hydroxy-3-[4-methoxy-7-(3-methylbut-2-enyl)-1,3-benzoxazol-6-yl]chromen-4-one

1 reference

5,7-Dihydroxy-3-[3-(3-hydroxy-3-methylbut-1-enyl)-4,5-dimethoxyphenyl]chromen-4-one

1 reference

5,7-Dihydroxy-3-[4-hydroxy-2-(2-hydroxypropan-2-yl)-5-methoxy-1-benzofuran-7-yl]chromen-4-one

1 reference

1 reference

1,3,8-Trihydroxy-7-(3-hydroxy-3-methylbutyl)-9-methoxy-[1]benzofuro[2,3-b]chromen-11-one

1 reference

5,7-dihydroxy-3-[(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-7-yl]chromen-4-one

1 reference

(16S)-5,7,16-trihydroxy-20-methoxy-17,17-dimethyl-10,12,18-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4,6,8,13,19-heptaen-3-one

1 reference

5,7-dihydroxy-3-[(2R)-7-hydroxy-2-(2-hydroxypropan-2-yl)-6-methoxy-5-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-4-yl]chromen-4-one

1 reference

1 reference

3-[(3R)-3,5-dihydroxy-8-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-5,7-dihydroxychromen-4-one

1 reference

5,7-dihydroxy-3-[(2S)-7-hydroxy-2-(2-hydroxypropan-2-yl)-6-methoxy-5-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-4-yl]chromen-4-one

1 reference

1 reference

5,7-Dihydroxy-3-[7-hydroxy-2-(2-hydroxypropan-2-yl)-6-methoxy-5-(3-methylbut-2-enyl)-1-benzofuran-4-yl]chromen-4-one

1 reference

2'-deoxypiscerythrone

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Satoshi Tahara

1

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2990825-2

Masaaki Moriyama

series ordinal

2

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2990825-2

John L. Ingham

series ordinal

3

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2990825-2

Junya Mizutani

series ordinal

4

1 reference

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2990825-2

publication date

August 1993

1 reference

16 September 2022

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2990825-2

volume

34

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2990825-2

issue

1

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2990825-2

page(s)

303-315

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2990825-2

cites work

Some New Constituents of Piscidia erythrina L.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Über die Inhaltsstoffe vonPiscidia eryfhrina L

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

The extractives of piscidia erythrina L.—I

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

The extractives of piscidia erythrina L.—III

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Two isoflavones from Piscidia erythrina

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Major isoflavonoids of the jamaican dogwood Piscidia erythrina

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Further flavonoids from Piscidia erythrina

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Isoflavonoids from the Root Bark of Piscidia erythrina and a Note on the Structure of Piscidone

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

New Rotenoids from the Root Bark of Jamaican Dogwood (Piscidia erythrina L.)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

5,7,3′,4′,5′-pentaoxygenated and 2′,6′-diprenylated isoflavones from Piscidia erythrina

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Isoflavones from the root bark of Piscidia erythrina

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

The first naturally occurring amino-isoflavone from the root bark of L.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Isoflavonoid alkaloids from Piscidia erythrina

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Naturally Occurring Coumaranochroman-4-Ones: A New Class Of Isoflavonoids From Lupins And Jamaican Dogwood

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Structure revision of piscidone, a major isoflavonoid in the root bark of Piscidia erythrina

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Isoflavonoids of Dalbergia paniculata seeds

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

New coumaronochromones from white lupin, Lupinus albus L. (Leguminosae).

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Transformation of the diprenylated isoflavone 2'-hydroxylupalbigenin by Aspergillus flavus.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Fungitoxic dihydrofuranoisoflavones and related compounds in white lupin, Lupinus albus

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Revised Structures of Broussoflavonols C and D, and the Structure of Broussoflavonol E

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Coumarins and other constituents of Hesperethusa crenulata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

8-C-Prenylflavonoids from the seed of Tephrosia bracteolata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Structure Elucidation of Kwakhurin, a New Prenylated Isoflavone from Pueraria miriflca Roots

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Plant antimutagenic agents, 5. Isolation and structure of two new isoflavones, fremontin and fremontone from Psorothamnus fremontii

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Induction of phytoalexin synthesis in soybean: Enzymatic cyclization of prenylated pterocarpans to glyceollin isomers

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Elicitor-induced biosynthesis of psoralens in Ammi majus L. suspension cultures. Microsomal conversion of demethylsuberosin into (+)marmesin and psoralen.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Further Isoflavonoids from White Lupin Roots

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021

Prenyl bibenzyls from the liverworts Radula perrottetii and Radula complanata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2990825-2

7 January 2021