(Q42926316)

English

Bioassay-Guided Isolation of the Antidiabetic Principle from Sorbus decora (Rosaceae) Used Traditionally by the Eeyou Istchee Cree First Nations

scientific article published on September 24, 2010

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scholarly article

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Europe PubMed Central

PubMed publication ID

11 November 2017

Bioassay-guided isolation of the antidiabetic principle from Sorbus decora (Rosaceae) used traditionally by the Eeyou Istchee Cree First Nations (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

Bioassay-Guided Isolation of the Antidiabetic Principle from Sorbus decora (Rosaceae) Used Traditionally by the Eeyou Istchee Cree First Nations (English)

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

1 reference

1 reference

23-Hydroxybetulin

1 reference

1 reference

3a,8-Bis(hydroxymethyl)-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]chrysen-9-ol

1 reference

1 reference

3,4-Dihydroxy-trans-cinnamic acid 23,28-dihydroxyurs-12-ene-3beta-yl ester

1 reference

Urs-12-ene-3beta,23,28-triol

1 reference

[4,8a-bis(hydroxymethyl)-4,6a,6b,11,12,14b-hexamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate

1 reference

Lup-20(29)-ene-3beta,28-diol

1 reference

(−)-epicatechin

1 reference

1 reference

Lup-20(29)-en-28-oic acid, 3beta-hydroxy-

1 reference

1 reference

1 reference

Urs-12-ene-3,28-diol, (3beta)-

1 reference

1 reference

4,8a-bis(hydroxymethyl)-4,6a,6b,11,12,14b-hexamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol

1 reference

3,4-Dihydroxy-trans-cinnamic acid 23,28-dihydroxylupa-20(29)-ene-3beta-yl ester

1 reference

[3a,8-Bis(hydroxymethyl)-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]chrysen-9-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate

1 reference

0 references

6

object named as

Tony Durst

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

author name string

Louis Martineau

2

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

Ammar Saleem

3

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

Padma Madiraju

4

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

Asim Muhammad

5

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

Pierre Haddad

7

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

John Thor Arnason

8

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

José A. Guerrero-Analco

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:20738101

23 June 2024

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20738101

23 June 2024

publication date

25 August 2010

1 reference

16 September 2022

24 September 2010

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20738101

23 June 2024

full work available at URL

https://pubs.acs.org/doi/pdf/10.1021/np1003005

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Journal of Natural Products

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

73

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

1519-1523

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

THE CHEMICAL COMPOSITION OF THE WOOD EXTRACTIVES OF SORBUS DECORA (SARG.) SCHNEID.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1139/V62-170

Plants used by the Cree Nation of Eeyou Istchee (Quebec, Canada) for the treatment of diabetes: A novel approach in quantitative ethnobotany

3

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Selected plant species from the Cree pharmacopoeia of northern Quebec possess anti-diabetic potential

4

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Medicinal plants of Cree communities (Québec, Canada): antioxidant activity of plants used to treat type 2 diabetes symptoms

5

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Evaluation of the antidiabetic potential of selected medicinal plant extracts from the Canadian boreal forest used to treat symptoms of diabetes: part II.

6

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Triterpene caffeates from bark of Betula pubescens

8

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Triterpene caffeoyl esters and diterpenes from Celastrus stephanotifolius

9

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Two bioactive pentacyclic triterpene esters from the root bark of Hibiscus syriacus

10

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Activity-guided isolation of triterpenoid acyl CoA cholesteryl acyl transferase (ACAT) inhibitors from Ilex kudincha

11

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Four new triterpenoids from Maytenus ilicifolia

12

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Activity of lupane triterpenoids from Maytenus species as inhibitors of nitric oxide and prostaglandin E2.

13

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Structural constraints and the importance of lipophilicity for the mitochondrial uncoupling activity of naturally occurring caffeic acid esters with potential for the treatment of insulin resistance

14

1 reference

10.1021/NP1003005

https://api.crossref.org/works/10.1021/NP1003005

23 June 2024

Identifiers

10.1021/NP1003005

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

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