(Q104838326)

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Cytotoxic Components from the Leaves ofSchefflera Taiwaniana

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Cytotoxic Components from the Leaves ofSchefflera Taiwaniana (English)

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reference URL

http://api.crossref.org/works/10.1002%2Fjccs.200200067

main subject

Schefflera taiwaniana

1 reference

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tetracosyl (2Z)-3-(4-hydroxyphenyl)prop-2-enoate

1 reference

inferred from

reverse claim

[(9Z,11S,16S)-11,16-dihydroxyoctadeca-9,17-dien-12,14-diynyl] acetate

1 reference

inferred from

reverse claim

hexacosyl (2Z)-3-(4-hydroxyphenyl)prop-2-enoate

1 reference

inferred from

reverse claim

(1S,4R,4aS,8aS)-4,8a-dimethyl-6-propan-2-yl-1,2,3,4a,5,8-hexahydronaphthalene-1,4-diol

1 reference

inferred from

reverse claim

(S)-2,7,8-Trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-ol

1 reference

inferred from

reverse claim

dimethyl (3R,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate

1 reference

inferred from

reverse claim

tetracosyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

1 reference

inferred from

reverse claim

(3S,8R)-heptadeca-1,9-dien-4,6-diyne-3,8-diol

1 reference

1 reference

1,4a-Dimethyl-7-(propan-2-yl)-1,2,3,4,4a,5,8,8a-octahydronaphthalene-1,4-diol

1 reference

inferred from

reverse claim

docosyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

1 reference

1 reference

dimethyl (1R,3aS,5aR,5bR,7aR,8S,9R,11aR,11bR,13aR,13bR)-9-hydroxy-5a,5b,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylate

1 reference

1 reference

1 reference

(4aS,6aS,6bR,8aR,9R,10R,12aR,12bR,14bS)-10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

1 reference

1 reference

Yueh-Hsiung Kuo

1

1 reference

reference URL

http://api.crossref.org/works/10.1002%2Fjccs.200200067

Jir-Mehng Lo

series ordinal

2

1 reference

reference URL

http://api.crossref.org/works/10.1002%2Fjccs.200200067

Yih-Fwu Chan

series ordinal

3

1 reference

reference URL

http://api.crossref.org/works/10.1002%2Fjccs.200200067

publication date

June 2002

1 reference

16 September 2022

Journal of the Chinese Chemical Society

1 reference

reference URL

http://api.crossref.org/works/10.1002%2Fjccs.200200067

volume

49

1 reference

reference URL

http://api.crossref.org/works/10.1002%2Fjccs.200200067

issue

3

1 reference

reference URL

http://api.crossref.org/works/10.1002%2Fjccs.200200067

page(s)

427-431

1 reference

reference URL

http://api.crossref.org/works/10.1002%2Fjccs.200200067

cites work

Polyacetylenverbindungen, 220. Über die Inhaltsstoffe vonSmyrnium olusatrum L.

2 references

9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/CBER.19731061120

9 March 2024

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A sulphated triterpenoid saponin from Schefflera octophylla

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Extractive components from the wood of Taiwania cryptomerioides Hayata: the structures of “T-cadinol” and “T-murrolol”

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Rugosal A and related carotane sesquiterpenes in the glandular trichome exudate of Rosa rugosa

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9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

A triterpene and saponin from roots of Ilex pubescens

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9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Two triterpenoid carboxylic acids from Acanthopanax trifoliatus

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9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Sesquiterpene alcohols and triterpenoids from Liatris microcephala

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Tocotrienols from Iryanthera grandis

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

The polyacetylenic falcarinol as the major allergen in schefflera arboricola

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

A bidesmosidic triterpenoid saponin from Schefflera octophylla

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9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Antiproliferative constituents from umbelliferae plants. V. A new furanocoumarin and falcarindiol furanocoumarin ethers from the root of Angelica japonica

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Oleanane and ursane glycosides from Schefflera octophylla

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Triterpenoids and their glycosides from the bark of Schefflera octophylla

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Triterpenes from Tripterigium wilfordii

1 reference

9 March 2024

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Immunosuppressive activity of a monoterpene from Eucommia ulmoides

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Two new triterpenoid glycosides from the leaves of Schefflera octophylla.

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Isoprenylated flavonols of formosan Broussonetia papyrifera

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Two new triterpenoid sulfates from the leaves of Schefflera octophylla.

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

3α,11α-Dihydroxylup-20(29)-ene-23,28-dioic acid from Schefflera octophylla

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

Two naturally occurring acyclic diterpene and norditerpene aldehydes from Tetragonia tetragonoides

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/JCCS.200200067

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DOI

10.1002/JCCS.200200067

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(Q104838326)

Cytotoxic Components from the Leaves ofSchefflera Taiwaniana

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