Diterpenes and sesquiterpenes from the bark of Taxus yunnanensis (Q79185125)

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20 December 2019

title

Diterpenes and sesquiterpenes from the bark of Taxus yunnanensis (English)

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20 December 2019

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10-Deacetylcephalomannine

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[(1S,2S,3S,5S,8S,10S,14S)-2,5,10-triacetyloxy-8,12,15,15-tetramethyl-4-methylidene-14-tricyclo[9.3.1.03,8]pentadec-11-enyl] (2R,3S)-3-hydroxy-2-methylbutanoate

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1beta-Acetoxy-7-drimen-11-ol-11,12-lactone

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[(1S,3R,5R,8R,9R,10R,13R,14R)-9,10,13-triacetyloxy-14-hydroxy-8,12,15,15-tetramethyl-4-methylidene-5-tricyclo[9.3.1.03,8]pentadec-11-enyl] acetate

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3aalpha,4,9,9abeta-Tetrahydro-4alpha-(3-methoxy-4-hydroxyphenyl)6-hydroxy-7-methoxynaphtho[2,3-c]furan-1(3H)-one

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[(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-diacetyloxy-1,9-dihydroxy-15-[(2S,3R)-2-hydroxy-3-[[(E)-2-methylbut-2-enoyl]amino]-3-phenylpropanoyl]oxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate

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[(1S,2S,4S,7R,8R,9S,10R,12R,13R,16R)-4,10,13-triacetyloxy-7,12-dihydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-8-yl] benzoate

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(E)-4-hydroxy-3-methoxycinnamaldehyde

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1beta-Acetoxy-6-drimen-8alpha,11alpha-diol

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Taxus yunnanensis

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4-[4-[(4-Hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]benzene-1,2-diol

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[(1S,3S,8S)-7,9,10,13-tetraacetyloxy-8,12,15,15-tetramethyl-4-methylidene-5-tricyclo[9.3.1.03,8]pentadec-11-enyl] 3-phenylprop-2-enoate

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(1R,2R,3R,5S,7S,8S,9R,10R)-2,7,9,10-tetrakis(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxotricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2E)-3-phenylprop-2-enoate

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7-(beta-Xylosyl)taxol C

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(1R,3R,8S)-2,5,10-tris(acetyloxy)-8,12,15,15-tetramethyl-4-methylidenetricyclo[9.3.1.0³,⁸]pentadec-11-en-14-yl 3-hydroxy-2-methylbutanoate

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2,3-Naphthalenedimethanol, 1-(3,4-dihydroxyphenyl)-1,2,3,4-tetrahydro-7-hydroxy-6-methoxy-, stereoisomer (8CI); (1S,2R,3R)-1-(3,4-Dihydroxyphenyl)-1,2,3,4-tetrahydro-7-hydroxy-6-methoxy-2,3-naphthalenedimethanol

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[(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-diacetyloxy-1,9-dihydroxy-15-[(2R)-2-hydroxy-3-(2-methylbutanoylamino)-3-phenylpropanoyl]oxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate

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(1-Hydroxy-6,6,9a-trimethyl-1,3,5,5a,7,8,9,9b-octahydrobenzo[e][2]benzofuran-9-yl) acetate

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10-deacetylpaclitaxel

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[(2R,3R,5S,7S,8S,9R,10R,13S)-2,7,9,10,13-pentaacetyloxy-8,12,15,15-tetramethyl-4-methylidene-5-tricyclo[9.3.1.03,8]pentadec-11-enyl] (E)-3-phenylprop-2-enoate

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2-(4-Hydroxy-3-methoxyphenyl)-4-(alpha-hydroxy-4-hydroxy-3-methoxybenzyl)tetrahydrofuran-3-methanol

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3,5a,9-Trimethyl-3a-propan-2-yl-1,2,3,4,5,6,7,8,9,9a,10,10a-dodecahydrobenzo[f]azulene

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Decinnamoyltaxinine J

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[10-Acetyloxy-4,6,8-trihydroxy-10a-(2-hydroxypropan-2-yl)-3,5a-dimethyl-9-methylidene-2-oxo-1,4,5,6,7,8,9a,10-octahydrobenzo[g]azulen-5-yl] benzoate

10-deacetylbaccatin III

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1-acetoxy-5-deacetyl-baccatinI

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(2,5,7,9-Tetrahydroxy-8,12,15,15-tetramethyl-4-methylidene-13-oxo-10-tricyclo[9.3.1.03,8]pentadec-11-enyl) acetate

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Taxus wallichiana var. wallichiana

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https://api.crossref.org/works/10.1016/S0031-9422(03)00503-X

23 March 2024

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https://api.crossref.org/works/10.1016/S0031-9422(03)00503-X

23 March 2024

1

Nhan Trung Nguyen

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14568081

23 March 2024

author name string

Yasuhiro Tezuka

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14568081%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

Takahiro Nobukawa

4

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14568081%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

Shigetoshi Kadota

5

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14568081%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

Arjun H. Banskota

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14568081

23 March 2024

language of work or name

English

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14568081

23 March 2024

publication date

November 2003

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16 September 2022

7

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full work available at URL

inferred from page(s)

https://api.elsevier.com/content/article/PII:S003194220300503X?httpAccept=text/xml

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https://api.crossref.org/works/10.1016/S0031-9422(03)00503-X

https://api.elsevier.com/content/article/PII:S003194220300503X?httpAccept=text/plain

23 March 2024

1 reference

https://api.crossref.org/works/10.1016/S0031-9422(03)00503-X

23 March 2024

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14568081%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

volume

64

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14568081%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

issue

6

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14568081%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

page(s)

1141-1147

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14568081%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

cites work

The taxane diterpenoids

1 reference

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7 January 2021

Three new C-14 oxygenated taxanes from the wood of Taxus yunnanensis

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7 January 2021

Taxol analogues from the roots of Taxus x media

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7 January 2021

A taxane from the himalayan yew, Taxus wallichiana

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7 January 2021

Mixed acetoxy-benzoxy taxane esters from Taxus brevifolia

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7 January 2021

The taxoids. Comparative clinical pharmacology and therapeutic potential

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7 January 2021

Direct enantiomeric separation of flavanones by high performance liquid chromatography using various chiral stationary phases

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7 January 2021

Structures of nine new diterpenoids from Taxus chinensis

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https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900503-X

7 January 2021

New taxanes from Taxus brevifolia, 2

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7 January 2021

New taxanes from Taxus brevifolia

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7 January 2021

A new drimane from the heartwood of the Japanese yew, Taxus cuspidata

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7 January 2021

Taxuspine D, a new taxane diterpene from Taxus cuspidata with potent inhibitory activity against Ca(2+)-induced depolymerization of microtubules

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7 January 2021

Taxuspines E ∼ H and J, new taxoids from the Japanese yew Taxus cuspidata

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7 January 2021

Taxuyunnanines S-V, new taxoids from Taxus yunnanensis

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7 January 2021

A new 1,2-deoxytaxane diterpenoid from Taxus chinensis

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7 January 2021

Two taxane diterpenes from Taxus mairei

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7 January 2021

Yunnanxane and its homologous esters from cell cultures of Taxus chinensis var. mairei

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7 January 2021

19-Hydroxybaccatin III, 10-Deacetylcephalomannine, and 10-Deacetyltaxol: New Antitumor Taxanes From Taxus wallichiana

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7 January 2021

Taxoids from Taxus cuspidata var. nana

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7 January 2021

14 β-Hydroxytaxusin, a New Taxane from Taxus Mairei

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7 January 2021

Two new taxanes from Taxus chinensis var. mairei

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7 January 2021

Microbial and reducing agents catalyze the rearrangement of taxanes

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7 January 2021

Three New Taxane Diterpenoids from Needles and Stems of Taxus cuspidata

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7 January 2021

Taxezopidines B−H, New Taxoids from Japanese YewTaxus cuspidata

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7 January 2021

Plant antitumor agents. VI. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia

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7 January 2021

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7 January 2021

Studies on the chemical constituents of Taxus yunnanensis

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2-Deacetoxytaxinine B: a taxane diterpenoid from Taxus chinensis

23 March 2024

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Nuclear Overhauser effect, a unique method of defining the relative stereochemistry and conformation of taxane derivatives

23 March 2024

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23 March 2024

Identifiers

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14568081%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

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