Phenolic compounds from the branches of Eucalyptus maideni (Q39410724)

11 September 2017

Phenolic compounds from the branches of Eucalyptus maideni (English)

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1-[2,4-Dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone

11 September 2017

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3-Methylellagic acid 8-rhamnoside

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engeletin (unspec. stereochem.)

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17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

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4-[2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,2-diol

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1 reference

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beta-Hydroxypropiovanillone

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2,4,6-Trihydroxy-5-[1-(4-hydroxy-1,1,4,7-tetramethyl-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-yl)-3-methylbutyl]benzene-1,3-dicarbaldehyde

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1,2,3,5-tetrahydroxybenzene

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(3S)-3-hydroxy-5-(4-hydroxy-3-methoxyphenyl)pentanoic acid

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2-(4-Hydroxy-3-methoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

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4-[(4S,6S)-4-hydroxy-2,6-dimethyl-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohexen-1-yl]butan-2-one

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8-beta-D-Glucopyranosyl-5,7-dihydroxy-2-(2-methylpropyl)-4H-1-benzopyran-4-one

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2-Acetyl-3,5-dihydroxyphenyl hexopyranoside

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1 reference

(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol

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3alpha-(alpha-L-Rhamnopyranosyloxymethyl)-4beta-(3,5-dimethoxy-4-hydroxyphenyl)-5,7-dimethoxy-6-hydroxytetralin-2beta-methanol

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Li-Wen Tian

1

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11 September 2017

Min Xu

2

1 reference

11 September 2017

Yan Li

3

1 reference

11 September 2017

Xing-Yao Li

4

1 reference

11 September 2017

Dong Wang

5

1 reference

11 September 2017

Hong-Tao Zhu

6

1 reference

11 September 2017

Chong-Ren Yang

7

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11 September 2017

Ying-Jun Zhang

8

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Chemistry and Biodiversity

11 September 2017

January 2012

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16 September 2022

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11 September 2017

9

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11 September 2017

123-130

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11 September 2017

1

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Bioactive acylphloroglucinol derivatives from Eucalyptus species

11 September 2017

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https://api.crossref.org/works/10.1002%2FCBDV.201100021

Eucalmaidins A-E, (+)-oleuropeic acid derivatives from the fresh leaves of Eucalyptus maideni

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Phloroglucinol glycosides from the fresh fruits of Eucalyptus maideni

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Three xanthones and a benzophenone from Garcinia mangostana

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Kinase inhibitors from Polygonum cuspidatum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Cypellocarpins A-C, phenol glycosides esterified with oleuropeic acid, from Eucalyptus cypellocarpa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Dimeric flavonol glycoside and galloylated C-glucosylchromones from Kunzea ambigua

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Novel detection of formylated phloroglucinol compounds (FPCs) in the wound wood of Eucalyptus globulus and E. nitens

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Inhibitors of skin-tumor promotion. VIII. Inhibitory effects of euglobals and their related compounds on Epstein-Barr virus activation. (1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Anti-tumor-promoting activities of euglobals from Eucalyptus plants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Cancer chemopreventive activity of euglobal-G1 from leaves of Eucalyptus grandis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Antinociceptive properties of caffeic acid derivatives in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCBDV.201100021

Studies on the glycosides of Epimedium grandiflorum Morr. var. thunbergianum (Miq.) Nakai. II

21 January 2018

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

Monoterpene Glucosides from Cunila spicata

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

Macrocarpals: HIV-RTase inhibitors of Eucalyptus globulus

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

Caesaljapin, a cassane diterpenoid from Caesalpinia decapetala var. Japonica

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

A phloracetophenone glucoside from Rhododendron ferrugineum

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

The Chemistry of Eucalypt Kinos. IV. Eucalyptus hemiphloia Kino

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

Phenolics of Quercus rubra wood

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9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

Chemical Evaluation of Betula Species in Japan. I. Constituents of Betula ermanii.

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

Studies on rhubarb (rhei rhizoma). VI. Isolation and characterization of stilbenes.

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

Lignan Glycosides from the Heartwood of European Oak Quercus petraea

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

Cypellocarpin C and other compounds from the fruits of Eucalyptus globulus Labill.

1 reference

COCI

https://opencitations.net/index/api/v1/references/10.1002/CBDV.201100021

23 March 2024

Identifiers

DOI

10.1002/CBDV.201100021

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11 September 2017

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