(Q104859290)

http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2980083-6

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(R)-5-Hydroxy-1-(4-hydroxyphenyl)-7-phenyl-6-heptene-3-one

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2',4',4-Trihydroxy-6'-methoxychalcone

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(E,3R,5R)-7-(4-hydroxyphenyl)-1-phenylhept-1-ene-3,5-diol

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pinosylvin dimethyl ether

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3-methoxy-5-[(1Z)-2-phenylethenyl]phenol

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1,3-dimethoxy-5-(2-phenylethenyl)benzene

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(5R,6E)-5-hydroxy-1,7-diphenylhept-6-en-3-one

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3-[4-[5-Methoxy-1-(2-phenylethenyl)cyclohexa-2,4-dien-1-yl]-2,6,6-trimethyl-3-bicyclo[3.1.1]hept-1-enyl]-2,6,6-trimethyl-3-(2,6,6-trimethyl-3-bicyclo[3.1.1]hept-1-enyl)bicyclo[3.1.1]hept-1-ene

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(E)-1-(2,4-dihydroxy-6-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one

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(E/Z)-4-methoxyresveratrol

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Pinosylvin methyl ether

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3-methoxy-5-(2-phenylethenyl)phenol

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1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one

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(8S,E)-8,20-Epoxylabd-12-ene-15,16-dial

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(8S,12E,14E)-15-[3-[(E)-3-Phenylpropenoyl]-2,6-dihydroxy-4-methoxyphenyl]-8,20-epoxylabda-12,14-dien-16-one

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Labda-8(17),12-diene-15,16-dial

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1-methoxy-3-[(1R)-4-methyl-1-propan-2-ylcyclohex-3-en-1-yl]oxy-5-[(E)-2-phenylethenyl]benzene

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4,6,6-Trimethyl-3-[2,6,6-trimethyl-3-(2,6,6-trimethyl-3-bicyclo[3.1.1]hept-1-enyl)-3-bicyclo[3.1.1]hept-1-enyl]bicyclo[3.1.1]hept-4-en-2-ol

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dihydroxymethoxychalcone

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Koon-Sin Ngo

1

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2980083-6

Geoffrey D. Brown

series ordinal

2

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2980083-6

publication date

March 1998

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16 September 2022

7

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inferred from page(s)

published in

Phytochemistry

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2980083-6

volume

47

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2980083-6

issue

6

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2980083-6

page(s)

1117-1123

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2980083-6

cites work

Studies on the constituents of the seeds of Alpinia katsumadai Hayata.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Studies on the constituents of Alpinia. XII. On the constituents of the seeds of Alpinia katsumadai hayata. I. The structure of cardamomin

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Labdane and bisnorlabdane type diterpenes from Alpinia speciosa K. Schum.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Cytotoxic and Antifungal Diterpenes from the Seeds ofAlpinia galanga

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Isolation of flavonoids and a chalcone from Helichrysum odoratissimum and synthesis of helichrysetin

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Two new diarylheptanoids from Alpinia officinarum Hance.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Diarylheptanoids from the rhizomes of Curcuma xanthorrhiza and Alpinia officinarum.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Inhibitors of prostaglandin biosynthesis from Alpinia officinarum.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Studies on the Pungent Principle of Alpinia officinarum HANCE

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

A pungent principle from Alpinia oxyphylla

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Isolation of a Cardiotonic Principle fromAlpinia oxyphylla

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

A 17-Diarylheptanoid from Alpinia conchigera

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Phenolic compounds from the rhizomes of Alpinia speciosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Cardamonin and alpinetin from the seeds of Alpinia speciosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

New Diterpenes fromAlpinia galangaWILD.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

Diterpenes from the rhizomes of Alpinia formosana

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

The distribution of labdane diterpenes in the zingiberaceae of Malaysia

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021

"Three Novel Diarylheptanoids, Calyxin A, Calyxin B, and 3-EPI-Calyxin B from a Chinese Crude Drug\"Yunnan Cao Kou\"(Alpinia blepharocalyx K. SCHUM.)."

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2980083-6

7 January 2021