Alkyl, aryl, alkylarylquinoline, and related alkaloids (Q37034239)

17 August 2017

1 reference

title

Alkyl, aryl, alkylarylquinoline, and related alkaloids (English)

1 reference

17 August 2017

author name string

Maria Fátima das Graças Fernandes da Silva

1

1 reference

17 August 2017

Márcio Santos Soares

2

1 reference

17 August 2017

João Batista Fernandes

3

1 reference

17 August 2017

Paulo Cezar Vieria

4

1 reference

17 August 2017

publication date

1 January 2007

1 reference

The alkaloids. Chemistry and biology

17 August 2017

published in

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17 August 2017

volume

64

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17 August 2017

page(s)

139-214

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17 August 2017

cites work

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A New Alkaloid, Montanine, from Ruta Montana

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Quinolone alkaloids with inhibitory activity against nuclear factor of activated T cells from the fruits of Evodia rutaecarpa

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Biological Activity of Quinoline Alkaloids from Raulinoa echinata and X-ray Structure of Flindersiamine

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Limonoids and quinolone alkaloids from Evodia rutaecarpa Bentham.

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Quinoline alkaloids from the fruits of Evodia officinalis

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Quinolone alkaloids, diacylglycerol acyltransferase inhibitors from the fruits of Evodia rutaecarpa.

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Evocarpin, a new alkaloid from Evodia rutaecarpa

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Alkaloids from Dictyoloma vandellianum: their chemosystematic significance.

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An Examination of the Rutaceae of Hong Kong. VI. Graveoline, A New Alkaloid from Ruta graveolens

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Angustifolin, a coumarin from Ruta angustifolia

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Alkaloids of Lunasia amara Blanco. Isolation Studies

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Alkaloids of the Australian Rutaceae: Lunasia quercifolia. I. 7-Methoxy-1-methyl-2-4-quinolone

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Rat small intestine muscle relaxation alkaloids from Orixa japonica leaves

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Antimutagenic Constituents ofCasimiroa eduliswith Potential Cancer Chemopreventive Activity

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Quinoline alkaloids. Part XII. Alkaloids and coumarins of Orixa japonica thunb. Identification of a new quinoline alkaloid, orixinone

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Alkaloids from Galipea officinalis

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New quinoline alkaloids from Ruta chalepensis.

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Melochinone, a novel quinolinone from Melochia tomentosa L

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An unusual quinolinone alkaloid from Waltheria douradinha

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Antibiotic Metabolites from a Marine Pseudomonad

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2-n-Pentyl-4-quinolinol produced by a marine Alteromonas sp. and its potential ecological and biogeochemical roles

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2-Heptyl-4-hydroxyquinoline N-oxide, an antistaphylococcal agent produced by Pseudomonas aeruginosa

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Secondary metabolites by chemical screening. I. Calcium 3-hydroxyquinoline-2-carboxylate from a Streptomyces

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Helquinoline, a new tetrahydroquinoline antibiotic from Janibacter limosus Hel 1+.

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The Pseudomonas siderophore quinolobactin is synthesized from xanthurenic acid, an intermediate of the kynurenine pathway

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Trididemnic acids A and B, aromatic alkaloids from the northeastern pacific ascidian Trididemnum sp.

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Quinolobactin, a new siderophore of Pseudomonas fluorescens ATCC 17400, the production of which is repressed by the cognate pyoverdine

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Metabolites from the Sponge-Associated Bacterium Pseudomonas Species

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4-Hydroxymethyl-quinoline from Polyporus species

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Two quinoline alkaloids from the Caribbean cyanobacterium Lyngbya majuscula

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Perspicamides A and B, quinolinecarboxylic acid derivatives from the Australian ascidian Botrylloides perspicuum.

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Biosynthetic pathway of Pseudomonas aeruginosa 4-hydroxy-2-alkylquinolines

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Plant growth promoting and fungicidal 4-quinolinones from Pseudomonas cepacia

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2-(2-Heptenyl)-3-methyl-4-quinolinol from a Pseudomonas

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YM-30059, a novel quinolone antibiotic produced by Arthrobacter sp

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Quinolactacins A, B and C. Novel Quinolone Compounds from Penicillium sp. EPF-6. I. Taxonomy, Production, Isolation and Biological Properties.

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Quinolactacins A1 and A2, new acetylcholinesterase inhibitors from Penicillium citrinum

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Quinolactacide, a new quinolone insecticide from Penicillium citrinum Thom F 1539.

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Concise enantioselective syntheses of quinolactacins A and B through alternative Winterfeldt oxidation

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Functions required for extracellular quinolone signaling by Pseudomonas aeruginosa

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Analysis of Pseudomonas aeruginosa 4-hydroxy-2-alkylquinolines (HAQs) reveals a role for 4-hydroxy-2-heptylquinoline in cell-to-cell communication

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Zur Biosynthese der 2-n-Alkyl-4-hydroxychinolinderivate (Pseudane) bei Pseudomonas aeruginosa

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7 January 2021

Interference with Pseudomonas quinolone signal synthesis inhibits virulence factor expression by Pseudomonas aeruginosa

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Functional genetic analysis reveals a 2-Alkyl-4-quinolone signaling system in the human pathogen Burkholderia pseudomallei and related bacteria.

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Lignans, neolignans, and related compounds

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Broussonetine, a bisquinolyl-γ-butyrolactone from Broussonetia zeylanica

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Zur biosynthese des graveolins bei Ruta angustifolia

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Biomimetric total synthesis of quinolactacin B, TNF production inhibitor, and its analogs

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Über Inhaltsstoffe vonMelochia pyramidata L.

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Benzastatins A, B, C, and D: new free radical scavengers from Streptomyces nitrosporeus 30643. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological activities.

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Benzastatins A, B, C, and D: new free radical scavengers from Streptomyces nitrosporeus 30643. II. Structural determination

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https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Plant natural products with leishmanicidal activity

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Three new species of Galipea (Rutaceae, Galipeinae) from Brazil

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

2-substituted quinoline alkaloids as potential antileishmanial drugs

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

The activity of 2-substituted quinoline alkaloids in BALB/c mice infected with Leishmania donovani.

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

In vivo efficacy of oral and intralesional administration of 2-substituted quinolines in experimental treatment of new world cutaneous leishmaniasis caused by Leishmania amazonensis

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Natural products as trypanocidal, antileishmanial and antimalarial drugs

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Synthesis and biological evaluation of substituted quinolines: potential treatment of protozoal and retroviral co-infections.

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Decrease of intestinal P-glycoprotein activity by 2n-propylquinoline, a new oral treatment for visceral leishmaniasis

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Experimental treatment of chronic Trypanosoma cruzi infection in mice with 2-n-propylquinoline.

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

The effect of some 2-substituted quinolines isolated from Galipea longiflora on Plasmodium vinckei petteri infected mice

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Antiplasmodial and cytotoxic activity of galipinine and other tetrahydroquinolines from Galipea officinalis

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Molluscicide control of snail vectors of schistosomiasis

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

New citrinin derivatives isolated from Penicillium citrinum

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Anti-Helicobacter pylori activity of quinolone alkaloids from Evodiae fructus

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Highly selective antibacterial activity of novel alkyl quinolone alkaloids from a Chinese herbal medicine, Gosyuyu (Wu-Chu-Yu), against Helicobacter pylori in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

In vivo action of novel alkyl methyl quinolone alkaloids against Helicobacter pylori

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Screening of eight alkaloids and ten flavonoids isolated from four species of the genus Boronia (Rutaceae) for antimicrobial activities against seventeen clinical microbial strains

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Absence of the plasmid-mediated quinolone resistance qnrA gene among Campylobacter jejuni clinical isolates from Greece.

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Biologically active quinolone alkaloids from Evodia rutaecarpa on Artemia salina

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

New tetrahydroisoquinolinones from Hyeronima oblonga (Euphorbiaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Phytotoxins from the leaves of Ruta graveolens

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

New inhibitors of the quinol oxidation sites of bacterial cytochromes bo and bd.

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Inhibition of angiotensin II receptor binding by quinolone alkaloids fromEvodia rutaecarpa

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

1-methyl-2-undecyl-4(1H)-quinolone as an irreversible and selective inhibitor of type B monoamine oxidase

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Inhibition of leukotriene biosynthesis by quinolone alkaloids from the fruits of Evodia rutaecarpa

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Cytotoxic and Antiplatelet Aggregation Principles ofRuta Graveolens

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Substituted quinolines induce inhibition of proliferation of HTLV-1 infected cells

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Cytotoxicity and DNA topoisomerase inhibitory activity of constituents isolated from the fruits of Evodia officinalis

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Synthesis and antiplatelet activity of phenyl quinolones

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Synthesis of 4-alkoxy-2-phenylquinoline derivatives as potent antiplatelet agents.

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Synopses of Angostura Roem. & Schult. and Conchocarpus J. C. Mikan (Rutaceae)

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Phylogenetic relationships of Rutaceae: a cladistic analysis of the subfamilies using evidence from RBC and ATP sequence variation

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

A revised system of classification of the angiosperms

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Valid publication of names of prokaryotes according to the rules of nomenclature: past history and current practice

1 reference

https://api.crossref.org/works/10.1016%2FS1099-4831%2807%2964004-8

7 January 2021

Alkaloids of Haplophyllum acutifolium

1 reference

11 May 2024

https://opencitations.net/index/api/v1/citations/10.1007/BF00567972

Identifiers

DOI

10.1016/S1099-4831(07)64004-8

1 reference

17 August 2017

1 reference