Cytotoxic cardiac glycosides and coumarins from Antiaris toxicaria (Q35101095)

6 August 2017

Cytotoxic cardiac glycosides and coumarins from Antiaris toxicaria (English)

1 reference

(3R,5S,8R,9S,10S,13R,14S,17R)-5,14-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde

6 August 2017

1 reference

1 reference

1 reference

(3S,5R,8R,9S,10R,13R,14S,17R)-14-hydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-10-carbaldehyde

1 reference

3-[(3S,5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-10-(hydroxymethyl)-13-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one

1 reference

(3S,5S,8R,9S,10S,12R,13S,14S,17R)-5,12,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carboxylic acid

1 reference

1 reference

(5R,8R,9S,10S,12R,13S,14S,17R)-5,12,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde

1 reference

1 reference

1 reference

1 reference

1 reference

6-(2,3-Dihydroxy-3-methylbutyl)-8-hydroxy-7-methoxychromen-2-one

1 reference

1 reference

(3S,5S,8R,9S,10S,13R,14S,17R)-5,14-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde

1 reference

(3S,5S,8R,9S,10S,12R,13S,14S,17R)-5,12,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde

1 reference

1 reference

1 reference

3-[(3S,5R,8R,9S,10R,13R,14S,17R)-3,14-dihydroxy-10-(hydroxymethyl)-13-methyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one

1 reference

(1R,3aS,3bR,5aS,7S,9aS,9bS,11aR)-7-[(3,4-dihydroxy-6-methyl-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-4H-furan-3-yl)-dodecahydro-1H-cyclopenta[a]phenanthrene-9a-carbaldehyde

1 reference

1 reference

(9S,10R)-9-hydroxy-8,8-dimethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dihydropyrano[2,3-f]chromen-2-one

1 reference

1 reference

TZDYBTCOMXAYIA-BTBMPPRUSA-N

1 reference

(3S,5S,8R,9S,10S,12R,13S,14S,17R)-5,12,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carboxylic acid

1 reference

3-[(3S,5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-10,13-dimethyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one

1 reference

(3S,5R,8R,9S,10R,13R,14S,17R)-14-hydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-10-carboxylic acid

1 reference

1 reference

1 reference

(3S,5S,8R,9S,10S,12R,13S,14S,17R)-5,12,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde

1 reference

OFSZOCPGPLMCBG-MFYCUANCSA-N

1 reference

1 reference

9-Hydroxy-8,8-dimethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dihydropyrano[2,3-f]chromen-2-one

1 reference

3-[3-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-10-(hydroxymethyl)-13-methyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one

1 reference

(3S,5S,10R,13R,14S,17R)-14-hydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2R,5S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-10-carbaldehyde

1 reference

5,12,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde

1 reference

3-(4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl)oxy-5,12,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde

1 reference

3

Han-Dong Sun

1 reference

6 August 2017

Susan L Morris-Natschke

series ordinal

4

object named as

Susan L Morris-Natschke

1 reference

6 August 2017

5

Kuo-Hsiung Lee

1 reference

6 August 2017

Li-Shian Shi

1

1 reference

6 August 2017

Sheng-Chu Kuo

series ordinal

2

1 reference

6 August 2017

Tian-Shung Wu

series ordinal

6

1 reference

6 August 2017

language of work or name

English

0 references

publication date

6 February 2014

1 reference

full work available at URL

6 August 2017

https://cdr.lib.unc.edu/downloads/05741z733

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1016/j.bmc.2014.01.052?email=unpaywall_01@example.com

published in

Bioorganic & Medicinal Chemistry

1 reference

6 August 2017

22

1 reference

6 August 2017

6

1 reference

6 August 2017

1889-1898

1 reference

https://api.unpaywall.org/v2/10.1016/j.bmc.2014.01.052?email=unpaywall_01@example.com

6 August 2017

1 reference

19 March 2024

access restriction status

open access

1 reference

inferred from online access status

cites work

Toxicarioside M, a new cytotoxic 10β-hydroxy-19-nor-cardenolide from Antiaris toxicaria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334368

Cytotoxic cardenolide glycosides from the seeds of Antiaris toxicaria

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334368

Cardiac glycosides from Antiaris toxicaria with potent cardiotonic activity

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334368

Two new cytotoxic cardenolides from the latex of Antiaris toxicaria

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334368

A new cytotoxic 19-nor-cardenolide from the latex of Antiaris toxicaria

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334368

Novel therapeutic applications of cardiac glycosides

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334368

Cardiac glycosides as novel cancer therapeutic agents

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334368

Two antimicrobial flavanones from the leaves of Glycyrrhiza glabra

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334368

Chemical and antibacterial constituents of Skimmia anquetelia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334368

Cardiac glycosides from Erysimum cheiranthoides

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334368

Coumarins from Ferulago capillaris and F. brachyloba

27 September 2018

1 reference

12 December 2020

Antiproliferative cardiac glycosides from the latex of Antiaris toxicaria

1 reference

12 December 2020

Coumarin glycosides from Peucedanum japonicum

1 reference

12 December 2020

Coumarins and antiplatelet aggregation constituents from Formosan Peucedanum japonicum

1 reference

12 December 2020

Diplobifuranylones A and B, 5‘-Monosubstituted Tetrahydro-2H-bifuranyl-5-ones Produced byDiplodiacorticola, a Fungus Pathogen of Cork Oak

1 reference

12 December 2020

Cheritamine, A NewN-Fatty Acyl Tryptamine and Other Constituents from the Stems ofAnnona cherimola

1 reference

9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/JCCS.199900010

Seven Prenylphenols, Antiarones C, D, E, F, G, H, and I from the Root Bark of Antiaris toxicaria Lesch.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.3987/COM-90-5409

Two New prenylaurones, Antiarones A and B, from the Root Bark of Antiaris toxicaria Lesch

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.3987/COM-89-S103

Studies on the constituents of Ailanthus integrifolia

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.42.1669

Studies on coumarins from the root of Angelica decursiva FR. et SAV. II. Sterostructures of decursin, decursidin, and other new pyranocoumarin derivatives.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.23.20

Cardiac glycosides of Cheiranthus allioni. IX

1 reference

11 May 2024

https://opencitations.net/index/api/v1/citations/10.1007/BF00567852

Cardiac glycosides of Erysimum crepidifolium

1 reference

11 May 2024

https://opencitations.net/index/api/v1/citations/10.1007/BF00567853

Identifiers

DOI

10.1016/J.BMC.2014.01.052

1 reference

6 August 2017

1 reference

6 August 2017

1 reference