Isoprenylated flavanones from Morus cathayana (Q104947350)

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(3S,11R)-3,7,14-trihydroxy-18,18-dimethyl-11-(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one

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(1S,10R)-5-[(1S,5S,6R)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,4,6,14-tetrahydroxy-10-(3-methylbut-2-en-1-yl)-9,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-3,5,7,11,13,15-hexaen-2-one

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(3R,11R)-3,7,14-trihydroxy-18,18-dimethyl-11,21-bis(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one

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(5aR,10aS)-4-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one

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(5aR,10aR)-2-[(1R,5S,6R)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,5a,8-tetrahydroxy-10a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one

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(5aS,10aS)-1,3,8,10a-tetrahydroxy-5a-[(2Z,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-[1]benzofuro[3,2-b]chromen-11-one

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(5aS,10aR)-2-[(1S,5S,6R)-5-(2,4-dihydroxyphenyl)-6-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromene-6-carbonyl)-3-methylcyclohex-2-en-1-yl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one

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(3S,11S)-3,7,14-trihydroxy-18,18-dimethyl-11-(3-methylbut-2-enyl)-2,10,17-trioxapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),19-heptaen-12-one

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3,7,14-Trihydroxy-18,18-dimethyl-11-(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one

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2-[6-(2,4-Dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one

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3,7,14-Trihydroxy-18,18-dimethyl-11-(3-methylbut-2-enyl)-2,10,17-trioxapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),19-heptaen-12-one

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Toshio Fukai

1

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2897%2900564-5

Yue-Hu Pei

2

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Taro Nomura

3

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Chun-Quan Xu

4

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Li-Jun Wu

5

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Ying-Jie Chen

6

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publication date

January 1998

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16 September 2022

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volume

47

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issue

2

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page(s)

273-280

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cites work

Isoprenoid-substituted phenolic compounds of moraceous plants

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7 January 2021

Non-peptide bombesin receptor antagonists, kuwanon G and H, isolated from mulberry

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7 January 2021

On the Structure of Sanggenon Q, A New Diels-Alder Type Adduct from Morus mongolica Schneider

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7 January 2021

Components of the Root Bark of Morus cathayana. 1. Structures of Five New Isoprenylated Flavonoids, Sanggenols A - E and a Diprenyl-2-arylbenzofuran, Mulberrofuran V

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900564-5

7 January 2021

Three New Flavanone Derivatives from the Root Bark of Sorocea bonplandii Baillon

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900564-5

7 January 2021

Prenylated flavanones from Sorocea ilicifolia

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900564-5

7 January 2021

Variations in the chemical shift of the 5-hydroxyl proton of isoflavones; two isoflavones from licorice

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https://api.crossref.org/works/10.1016%2FS0031-9422%2897%2900564-5

7 January 2021