(Q35986942)

English

Geopyxins A-E, ent-kaurane diterpenoids from endolichenic fungal strains Geopyxis aff. majalis and Geopyxis sp. AZ0066: structure-activity relationships of geopyxins and their analogues

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Geopyxins A-E, ent-kaurane diterpenoids from endolichenic fungal strains Geopyxis aff. majalis and Geopyxis sp. AZ0066: structure-activity relationships of geopyxins and their analogues (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

1 reference

Pseudevernia intensa

1 reference

1 reference

2,11-dihydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid

1 reference

1 reference

1 reference

2-Hydroxy-5,9-dimethyl-14-methylidene-8,15-dioxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid

1 reference

2,8-Dihydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid

1 reference

Methyl 8-acetyloxy-2-hydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate

1 reference

1 reference

1 reference

2-Hydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid

1 reference

2,7,8-Trihydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid

1 reference

1 reference

2,8-Dihydroxy-14-(hydroxymethyl)-5,9-dimethyl-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid

1 reference

1-O-Acetylmethylgeopyxin A

1 reference

Methylgeopyxin A

1 reference

methylgeopyxin B

1 reference

(1R,2S,4S,5R,8S,9S,10S,13R,14S)-2,8-dihydroxy-14-(hydroxymethyl)-5,9-dimethyl-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid

1 reference

(1S,4R,4aS,6S,6aR,9R,11aS,11bS)-1,6-diacetoxy-4,11b-dimethyl-8-methylene-7-oxotetradecahydro-6a,9-methanocyclohepta[a]naphthalene-4-carboxylic acid

1 reference

Methyl 2,8-diacetyloxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate

1 reference

(1S,4R,4aS,6S,6aR,9R,11aS,11bS)-1-acetoxy-6-hydroxy-4,11b-dimethyl-8-methylene-7-oxotetradecahydro-6a,9-methanocyclohepta[a]naphthalene-4-carboxylic acid

1 reference

Methyl 2-hydroxy-5,9-dimethyl-14-methylidene-8,15-dioxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate

1 reference

Methyl 2,7,8-trihydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate

1 reference

Methyl 2,8-dihydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate

1 reference

Methyl 2-hydroxy-5,9-dimethyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate

1 reference

Methyl 2,8-dihydroxy-14-(hydroxymethyl)-5,9-dimethyl-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate

1 reference

9

object named as

Luke Whitesell

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Europe PubMed Central

PMC publication ID

11 August 2017

author name string

E M Kithsiri Wijeratne

1

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Bharat P Bashyal

2

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Manping X Liu

3

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Danilo D Rocha

4

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

G M Kamal B Gunaherath

5

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Jana M U'Ren

6

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Malkanthi K Gunatilaka

7

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

A Elizabeth Arnold

8

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

A A Leslie Gunatilaka

10

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

publication date

20 January 2012

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

full work available at URL

https://europepmc.org/articles/pmc3359839?pdf=render

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1021/np200769q?email=unpaywall_01@example.com

Journal of Natural Products

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

75

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

3

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

361-369

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

online access status

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1021/np200769q?email=unpaywall_01@example.com

access restriction status

1 reference

based on heuristic

inferred from online access status

Using the heat-shock response to discover anticancer compounds that target protein homeostasis

1 reference

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Smardaesidins A-G, isopimarane and 20-nor-isopimarane diterpenoids from Smardaea sp., a fungal endophyte of the moss Ceratodon purpureus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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Identity, regulation, and activity of inducible diterpenoid phytoalexins in maize

1 reference

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Proteomic approaches to the characterization of protein thiol modification

1 reference

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Quantitative reactivity profiling predicts functional cysteines in proteomes

1 reference

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1 reference

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1 reference

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Ent-kaurane diterpenoids from Rabdosia rubescens and their cytotoxic effects on human cancer cell lines

1 reference

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1 reference

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Heat shock factor 1 is a powerful multifaceted modifier of carcinogenesis

1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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1 reference

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1 reference

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1 reference

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Search for Hsp90 inhibitors with potential anticancer activity: isolation and SAR studies of radicicol and monocillin I from two plant-associated fungi of the Sonoran desert

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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Kaurane diterpenes from Isodon japonicus inhibit nitric oxide and prostaglandin E2 production and NF-kappaB activation in LPS-stimulated macrophage RAW264.7 cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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MODELTEST: testing the model of DNA substitution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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New hydroxylated ent-kauranoic acids from Eupatorium album

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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The first naturally occurring thiepinols and thienol from an endolichenic fungus Coniochaeta sp.

1 reference

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1 reference

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SIRT1 inhibitory diterpenoids from the Vietnamese medicinal plant Croton tonkinensis.

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Anti-HIV-1 diterpenoids from leaves and twigs of Polyalthia sclerophylla

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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Allenyl and alkynyl phenyl ethers from the endolichenic fungus Neurospora terricola

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

24 September 2018

Cytotoxic diterpenoids from Croton argyrophylloides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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Inhibition of NF-kappaB activation and iNOS induction by ent-kaurane diterpenoids in LPS-stimulated RAW264.7 murine macrophages

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3359839

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1 reference

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ent-kaurane diterpenoids from the liverwort Jungermannia atrobrunnea

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1 reference

https://pubmed.ncbi.nlm.nih.gov/22264149

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytotoxic 3,20-epoxy-ent-kaurane diterpenoids from Isodon eriocalyx var. laxiflora

1 reference

https://pubmed.ncbi.nlm.nih.gov/22264149

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytotoxic ent-kauranoids from the medicinal plant Isodon xerophilus

1 reference

https://pubmed.ncbi.nlm.nih.gov/22264149

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytotoxic Activity of Some Natural and Syntheticent-Kauranes⊥

1 reference

https://pubmed.ncbi.nlm.nih.gov/22264149

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/NP200769Q

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

ResearchGate publication ID

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