(Q28374035)

[1,6-Dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-13-(2-methylbutanoyloxy)-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] decanoate

1 reference

[14-Acetyloxy-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-methylbut-2-enoate

1 reference

[(1S,2R,6R,10R,11S,13S,14R,15R)-14-acetyloxy-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] decanoate

1 reference

[(1S,6R,14R,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-(2-methylbutanoyloxy)-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] dodecanoate

1 reference

12-O-Decanoylphorbol-13-(2-methylbutyrate)

1 reference

(13-Acetyloxy-1,6,14-trihydroxy-4,12,12,15-tetramethyl-5-oxo-8-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl)methyl octadeca-9,12-dienoate

1 reference

[1,6,14-Trihydroxy-4,12,12,15-tetramethyl-13-(2-methylbut-2-enoyloxy)-5-oxo-8-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl]methyl octadeca-9,12-dienoate

1 reference

[(1S,2R,6R,10R,11S,13S,14R,15R)-13-acetyloxy-1,6,14-trihydroxy-4,12,12,15-tetramethyl-5-oxo-8-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl]methyl (9Z,12Z)-octadeca-9,12-dienoate

1 reference

[(1S,6R,13S,14R,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-[(E)-2-methylbut-2-enoyl]oxy-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-methylbutanoate

1 reference

[(1S,2R,6R,10R,11S,13S,14R,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-[(E)-2-methylbut-2-enoyl]oxy-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] (2R)-2-methylbutanoate

1 reference

[(1S,2S,6R,10S,11R,13S,14R,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-[(E)-2-methylbut-2-enoyl]oxy-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] (2R)-2-methylbutanoate

1 reference

[(1S,2R,6R,10R,11S,13S,14R,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-[(2R)-2-methylbutanoyl]oxy-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] dodecanoate

1 reference

[(1S,2S,6R,10S,11R,13S,14R,15R)-14-acetyloxy-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] (E)-2-methylbut-2-enoate

1 reference

12-O-tetradecanoylphorbol-13-acetate

1 reference

[(1S,2R,6R,10R,11S,13S,14R,15R)-1,6,14-trihydroxy-4,12,12,15-tetramethyl-13-[(E)-2-methylbut-2-enoyl]oxy-5-oxo-8-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl]methyl (9E,12E)-octadeca-9,12-dienoate

1 reference

Phorbol acetate, caprate

1 reference

[(1S,2R,6R,10R,11S,13S,14R,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-13-[(2R)-2-methylbutanoyl]oxy-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] decanoate

1 reference

13-O-Acetylphorbol-20-(9Z,12Z)-octadecadienoate

1 reference

(1S,6R,13S,14R,15R)-14-(acetyloxy)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2Z)-2-methylbut-2-enoate

1 reference

13-O-Tigloylphorbol-20-linoleate

1 reference

1 reference

[(1S,2S,6R,10S,11R,13S,14R,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-13-[(2R)-2-methylbutanoyl]oxy-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] decanoate

1 reference

[1,6-Dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-14-(2-methylbut-2-enoyloxy)-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-methylbutanoate

1 reference

[14-Acetyloxy-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] decanoate

1 reference

[(1S,2R,6R,10R,11S,13S,14R,15R)-14-acetyloxy-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] (E)-2-methylbut-2-enoate

1 reference

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S El-Mekkawy

1

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M R Meselhy

2

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N Nakamura

3

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M Hattori

4

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T Kawahata

5

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T Otake

In vitro studies on the mode of action of the phorbol esters, potent tumor promoters: part 1.

6

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language of work or name

English

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publication date

February 2000

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16 September 2022

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53

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issue

4

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page(s)

457-64

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cites work

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https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

In vitro studies on the mode of action of the phorbol esters, potent tumor promoters, part 2.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

The phorbol ester TPA strongly inhibits HIV-1-induced syncytia formation but enhances virus production: possible involvement of protein kinase C pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

12-O-Tetradecanoylphorbol 13-acetate stimulates inositol lipid phosphorylation in intact human platelets

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

Inhibitory effects of Egyptian folk medicines on human immunodeficiency virus (HIV) reverse transcriptase

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

Anti-HIV-1 and anti-HIV-1-protease substances from Ganoderma lucidum

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

The irritant toxins of Blue Euphorbia (Euphorbia coerulescens Haw).

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

On the active principles of the spurge family. II. Skin irritant and cocarcinogenic factors from Euphorbia triangularis Desf. (author's transl)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

A nonpromoting phorbol from the samoan medicinal plant Homalanthus nutans inhibits cell killing by HIV-1

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

Plant anticancer agents. XXII. Isolation of a phorbol diester and its delta 5,6-7 beta-hydroperoxide derivative from Ostodes paniculata.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

Infection of HTLV-III/LAV in HTLV-I-carrying cells MT-2 and MT-4 and application in a plaque assay

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

Antileukemic Principles Isolated from Euphorbiaceae Plants

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

A new candidate for an anti-HIV-1 agent: modified cyclodextrin sulfate (mCDS71).

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

Anti-human immunodeficiency virus (anti-HIV) natural products with special emphasis on HIV reverse transcriptase inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

The role of protein kinase C in cell surface signal transduction and tumour promotion

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021

Phorbol derivatives from Sapium insigne

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2899%2900556-7

7 January 2021