(Q92879992)

English

Comprehensive Analysis of Secondary Metabolites in Usnea longissima (Lichenized Ascomycetes, Parmeliaceae) Using UPLC-ESI-QTOF-MS/MS and Pro-Apoptotic Activity of Barbatic Acid

scientific article published on 18 June 2019

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31216770%20AND%20SRC:MED&resulttype=core&format=json

2 May 2020

Comprehensive Analysis of Secondary Metabolites in Usnea longissima (Lichenized Ascomycetes, Parmeliaceae) Using UPLC-ESI-QTOF-MS/MS and Pro-Apoptotic Activity of Barbatic Acid (English)

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31216770%20AND%20SRC:MED&resulttype=core&format=json

2 May 2020

Usnea longissima

1 reference

Dolichousnea longissima

1 reference

(E)-9,10,12,13,15,16-hexahydroxyoctacos-18-enoic acid

1 reference

(E)-9,10,12,13,15,16-hexahydroxyheptacos-18-enoic acid

1 reference

(E)-9,10,12,13,14,15-hexahydroxytetracos-17-enoic acid

1 reference

2-(14-Carboxytetradecyl)-4-methyl-5-oxooxolane-3-carboxylic acid

1 reference

(15E,17E)-9,10,12,13-tetrahydroxyhenicosa-15,17-dienoic acid

1 reference

(2E)-6-acetyl-7,9-dihydroxy-8,9b-dimethyl-2-[1-(pentylamino)ethylidene]dibenzofuran-1,3-dione

1 reference

(2Z)-6-acetyl-7,9-dihydroxy-2-(1-methoxyethylidene)-8,9b-dimethyldibenzofuran-1,3-dione

1 reference

(E)-9,10,12,13,15,16-hexahydroxyhexacos-18-enoic acid

1 reference

2-(17-Carboxyheptadecyl)-4-methyl-5-oxooxolane-3-carboxylic acid

1 reference

apoptotic process

1 reference

based on heuristic

inferred from title

object named as

Parmeliaceae

1 reference

based on heuristic

inferred from title

secondary metabolite

1 reference

based on heuristic

inferred from title

1 reference

author name string

S Divya Reddy

1

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Europe PubMed Central

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2 May 2020

Bandi Siva

2

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Europe PubMed Central

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2 May 2020

Katragunta Kumar

3

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2 May 2020

V S Phani Babu

4

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2 May 2020

Vemireddy Sravanthi

5

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2 May 2020

V Lakshma Nayak

7

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2 May 2020

C H V Rao

9

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2 May 2020

B Sridhar

10

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2 May 2020

P Shashikala

11

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2 May 2020

K Suresh Babu

12

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2 May 2020

publication date

18 June 2019

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2 May 2020

full work available at URL

https://www.mdpi.com/1420-3049/24/12/2270/pdf?version=1560869264

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.3390/molecules24122270?email=unpaywall_01@example.com

1 reference

Europe PubMed Central

PMC publication ID

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2 May 2020

24

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2 May 2020

12

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2 May 2020

2270

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http://api.crossref.org/works/10.3390%2Fmolecules24122270

copyright license

Creative Commons Attribution 4.0 International

18 June 2019

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April 2022 Public Data File from Crossref

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online access status

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19 March 2024

https://api.unpaywall.org/v2/10.3390/molecules24122270?email=unpaywall_01@example.com

access restriction status

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based on heuristic

inferred from online access status

UPLC-MS/MS quantitative analysis and structural fragmentation study of five Parmotrema lichens from the Eastern Ghats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6630668

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Synthesis and biological evaluation of Schizandrin derivatives as potential anti-cancer agents.

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Synthesis and biological evaluation of imidazo[2,1-b]thiazole-benzimidazole conjugates as microtubule-targeting agents.

1 reference

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Rapid identification of limonoids from Cipadessa baccifera and Xylocarpus granatum using ESI-Q-ToF-MS/MS and their structure-fragmentation study.

1 reference

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Secondary Metabolite Profiling of Species of the Genus Usnea by UHPLC-ESI-OT-MS-MS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6630668

11 February 2021

Secondary metabolism in the lichen symbiosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6630668

11 February 2021

Metabolomic Analysis of Two Parmotrema Lichens: P. robustum (Degel.) Hale and P. andinum (Mull. Arg.) Hale Using UHPLC-ESI-OT-MS-MS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6630668

11 February 2021

Simultaneous determination of usnic, diffractaic, evernic and barbatic acids in rat plasma by ultra-high-performance liquid chromatography-quadrupole exactive Orbitrap mass spectrometry and its application to pharmacokinetic studies

1 reference

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Novel menadione hybrids: Synthesis, anticancer activity, and cell-based studies.

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Synthesis and biological evaluation of cis-restricted triazole/tetrazole mimics of combretastatin-benzothiazole hybrids as tubulin polymerization inhibitors and apoptosis inducers.

1 reference

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Recent (2000-2015) developments in the analysis of minor unknown natural products based on characteristic fragment information using LC-MS.

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11 February 2021

Usnic Acid Derivatives with Cytotoxic and Antifungal Activities from the Lichen Usnea longissima.

1 reference

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Optimisation and establishment of separation conditions of organic acids from Usnea longissima Ach. by pH-zone-refining counter-current chromatography: Discussion of the eluotropic sequence

1 reference

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Regulation of PSMB5 protein and β subunits of mammalian proteasome by constitutively activated signal transducer and activator of transcription 3 (STAT3): potential role in bortezomib-mediated anticancer therapy

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[Chemical constituents from Usnea longgisima, a traditional mongolian medicine]

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Cucurbitacin B induces apoptosis and S phase cell cycle arrest in BEL-7402 human hepatocellular carcinoma cells and is effective via oral administration

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Caspase-dependent apoptosis and -independent poly(ADP-ribose) polymerase cleavage induced by transforming growth factor beta1.

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Phosphatidylserine externalization during CD95-induced apoptosis of cells and cytoplasts requires ICE/CED-3 protease activity

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Complete NMR assignments of (+)-usnic acid

1 reference

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Lichens—a promising source of bioactive secondary metabolites

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Structural elucidation of 13-acetoxylichesterinic and 13-acetoxyprotolichesterinic acids, two aliphatic lichen metabolites from Neuropogon trachycarpus

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Mass spectrometry as a versatile ancillary technique for the rapid <i>in situ</i> identification of lichen metabolites directly from TLC plates

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Identifiers

10.3390/MOLECULES24122270

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Europe PubMed Central

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2 May 2020

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2 May 2020

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2 May 2020

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