(Q44285900)

1 December 2017

title

New minor taxanes analogues from the needles of Taxus canadenis (English)

1 reference

[(1R,2R,3S,4R,5R,6S,8S,10R,11R,12R,15S)-3,4,6,11-tetraacetyloxy-2,8-dihydroxy-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.02,15.05,10]heptadecan-5-yl]methyl acetate

1 December 2017

1 reference

1 reference

1 reference

[(1R,2R,3S,4R,5R,6S,8S,10R,11R,12R,15S)-3,4,6,11-tetraacetyloxy-2,8-dihydroxy-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.0^{2,15.0^{5,10]heptadecan-5-yl]methyl benzoate

1 reference

(2,3-Diacetyloxy-10-hydroxy-4,14,15,15-tetramethyl-8-methylidene-13-oxo-7-tetracyclo[9.3.1.01,9.04,9]pentadecanyl) 3-phenylprop-2-enoate

1 reference

Decinnamoyltaxagifine

1 reference

(2,3,10-Triacetyloxy-7-hydroxy-4,14,16,16-tetramethyl-8-methylidene-13-oxo-15-oxatetracyclo[9.4.1.01,14.04,9]hexadecan-5-yl) acetate

1 reference

1 reference

[(1R,2R,3S,4R,5S,6S,8S,10R,11R,12R,15S)-3,4,11-triacetyloxy-2,8-dihydroxy-1,5,15-trimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.02,15.05,10]heptadecan-6-yl] acetate

1 reference

1 reference

1 reference

[(1R,2S,3E,5R,8R,10R,13S)-2,10,13-triacetyloxy-8,12,15,15-tetramethyl-9-oxo-5-tricyclo[9.3.1.14,8]hexadeca-3,11-dienyl] (E)-3-phenylprop-2-enoate

1 reference

1 reference

[2,9,11,16-Tetraacetyloxy-5-hydroxy-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-8-yl] benzoate

1 reference

2-(16-Acetyloxy-2,5,11-trihydroxy-6,10-dimethyl-8,9-dioxo-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-3-yl)propan-2-yl benzoate

1 reference

(2-Acetyloxy-3,10,11-trihydroxy-4,14,15,15-tetramethyl-8-methylidene-13-oxo-7-tetracyclo[9.3.1.01,9.04,9]pentadecanyl) 3-phenylprop-2-enoate

1 reference

[(1S,2R,3R,4R,7S,9R,10S,11S,14S)-2-acetyloxy-3,10,11-trihydroxy-4,14,15,15-tetramethyl-8-methylidene-13-oxo-7-tetracyclo[9.3.1.01,9.04,9]pentadecanyl] (E)-3-phenylprop-2-enoate

1 reference

2alpha,13alpha-Diacetoxy-5alpha,7beta,10beta-trihydroxy-2,3-seco-2,20-cyclotaxa-4(20),11-dien-9-one

1 reference

(3,4,6,11-Tetraacetyloxy-2,8-dihydroxy-1,15-dimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.02,15.05,10]heptadecan-5-yl)methyl acetate

1 reference

(2,7,13-Triacetyloxy-10-hydroxy-8,12,15,15-tetramethyl-9-oxo-5-tricyclo[9.3.1.14,8]hexadeca-3,11-dienyl) 3-phenylprop-2-enoate

1 reference

[(1R,2R,3R,4R,7S,9S,10R,11R,14S)-2-acetyloxy-3,10-dihydroxy-4,14,15,15-tetramethyl-8-methylidene-13-oxo-7-tetracyclo[9.3.1.01,9.04,9]pentadecanyl] (E)-3-phenylprop-2-enoate

1 reference

1 reference

[(1R,2S,3R,4S,5S,7S,9R,10R,11R,14S)-3,5,10-triacetyloxy-2-hydroxy-4,14,16,16-tetramethyl-8-methylidene-13-oxo-15-oxatetracyclo[9.4.1.01,14.04,9]hexadecan-7-yl] (E)-3-phenylprop-2-enoate

1 reference

[(1R,2R,3R,4R,7S,9S,10R,11R,14S)-2,3-diacetyloxy-10-hydroxy-4,14,15,15-tetramethyl-8-methylidene-13-oxo-7-tetracyclo[9.3.1.01,9.04,9]pentadecanyl] (E)-3-phenylprop-2-enoate

1 reference

(11R,12S)-2alpha,7beta,9alpha,10beta-Tetraacetoxy-5alpha-hydroxy-11,12-epoxytax-4(20)-en-13-one

1 reference

1 reference

3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate

1 reference

1 reference

(3,5,10-Triacetyloxy-2-hydroxy-4,14,16,16-tetramethyl-8-methylidene-13-oxo-15-oxatetracyclo[9.4.1.01,14.04,9]hexadecan-7-yl) 3-phenylprop-2-enoate

1 reference

(1R,2S,3S,5S,8R,9R,10S,11S,13R,16S)-2,9,11,16-tetrakis(acetyloxy)-5-hydroxy-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.0³,⁷.0¹³,¹⁶]hexadec-6-en-8-yl benzoate

1 reference

(2,10,13-Triacetyloxy-8,12,15,15-tetramethyl-9-oxo-5-tricyclo[9.3.1.14,8]hexadeca-3,11-dienyl) 3-phenylprop-2-enoate

1 reference

3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one

1 reference

2-[(1R,2S,3S,5S,10S,11S,13R,16S)-16-acetyloxy-2,5,11-trihydroxy-6,10-dimethyl-8,9-dioxo-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-3-yl]propan-2-yl benzoate

1 reference

(2-Acetyloxy-3,10-dihydroxy-4,14,15,15-tetramethyl-8-methylidene-13-oxo-7-tetracyclo[9.3.1.01,9.04,9]pentadecanyl) 3-phenylprop-2-enoate

1 reference

Qing Wen Shi

1

1 reference

1 December 2017

Françoise Sauriol

series ordinal

2

1 reference

1 December 2017

Orval Mamer

series ordinal

3

1 reference

1 December 2017

Lolita O Zamir

series ordinal

4

1 reference

Bioorganic & Medicinal Chemistry

1 December 2017

language of work or name

English

0 references

publication date

January 2003

1 reference

16 September 2022

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1 December 2017

volume

11

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1 December 2017

issue

2

1 reference

1 December 2017

page(s)

293-303

1 reference

Taxus canadensis taxanes: structures and stereochemistry

1 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

New taxane analogues from the needles of Taxus canadensis

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Isolation of 9-Dihydro-13-acetylbaccatin III from Taxus canadensis

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Five novel taxanes from taxus canadensis

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Novel taxanes from the needles of Taxus canadensis

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Two new taxane diterpenoids from the seeds of the Chinese yew, Taxus yunnanensis

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Constituents of the yew trees.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Taxane diterpenoids from seeds of Taxus mairei

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Dantaxusins A and B, two new taxoids from Taxus yunnanensis.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Die Aufklärung von Taxin A ausTaxus baccata L

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Rearranged taxanes from Taxus baccata

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Rearranged taxoids from Taxus yunnanensis

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Taxuspines A ∼ C, new taxoids from Japanese yew Taxus cuspidata inhibiting drug transport activity of P-glycoprotein in multidrug-resistant cells

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Preparation of tubulin from brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Promotion of microtubule assembly in vitro by taxol

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

Taxuspines N, O, and P, new taxoids from Japanese yew Taxus cuspidata

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900347-4

7 January 2021

10.1016/S0968-0896(02)00347-4

Identifiers

DOI

1 reference

1 December 2017

1 reference