Multicomponent reaction-based synthesis and biological evaluation of tricyclic heterofused quinolines with multi-trypanosomatid activity

about

Synthesis and in vivo fungicidal activity of some new quinoline derivatives against rice blast.Discovery of a quinoline-based phenyl sulfone derivative as an antitrypanosomal agent.

P2860

Q50997284-63B049AA-8292-4E57-A498-AF07CDF2691A Q52612244-488F37EC-3520-4F0A-AB57-11D698265125

P2860

Multicomponent reaction-based synthesis and biological evaluation of tricyclic heterofused quinolines with multi-trypanosomatid activity

Item

http://www.wikidata.org/entity/Q36263511

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh

2015年學術文章

@zh-hant

name

Multicomponent reaction-based ...... multi-trypanosomatid activity

@ast

Multicomponent reaction-based ...... multi-trypanosomatid activity

@en

type

Item

label

Multicomponent reaction-based ...... multi-trypanosomatid activity

@ast

Multicomponent reaction-based ...... multi-trypanosomatid activity

@en

prefLabel

Multicomponent reaction-based ...... multi-trypanosomatid activity

@ast

Multicomponent reaction-based ...... multi-trypanosomatid activity

@en

P1476

Multicomponent reaction-based ...... multi-trypanosomatid activity

@en

P2093

Anna Lanzoni

http://www.w3.org/2001/XMLSchema#string

Belén Pérez

http://www.w3.org/2001/XMLSchema#string

Diana Berenguer

http://www.w3.org/2001/XMLSchema#string

Elisabet Viayna

http://www.w3.org/2001/XMLSchema#string

Esther Vicente-García

http://www.w3.org/2001/XMLSchema#string

Helena Sayago

http://www.w3.org/2001/XMLSchema#string

Irene Sola

http://www.w3.org/2001/XMLSchema#string

John M Kelly

http://www.w3.org/2001/XMLSchema#string

M Victòria Clos

http://www.w3.org/2001/XMLSchema#string

Rodolfo Lavilla

http://www.w3.org/2001/XMLSchema#string

P2860

Rescuing the bottom billion through control of neglected tropical diseases

Management of trypanosomiasis and leishmaniasis

A new and rapid colorimetric determination of acetylcholinesterase activity

Leishmaniasis: current status of available drugs and new potential drug targets

Recent developments in drug discovery for leishmaniasis and human African trypanosomiasis

Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings

A molecular mechanism for eflornithine resistance in African trypanosomes

Chagas disease

1,2,3,4-Tetrahydrobenzo[h][1,6]naphthyridines as a new family of potent peripheral-to-midgorge-site inhibitors of acetylcholinesterase: synthesis, pharmacological evaluation and mechanistic studies.

Knowledge-based approaches in the design and selection of compound libraries for drug discovery.

P304

120-137

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1016/J.EJMECH.2015.10.007

http://www.w3.org/2001/XMLSchema#string

P478

105

http://www.w3.org/2001/XMLSchema#string

P50

P577

2015-10-16T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

283012882

http://www.w3.org/2001/XMLSchema#string

P698

26479031

http://www.w3.org/2001/XMLSchema#string

P932

4638191

http://www.w3.org/2001/XMLSchema#string

Multicomponent reaction-based synthesis and biological evaluation of tricyclic heterofused quinolines with multi-trypanosomatid activity

about

P2860

P2860

Multicomponent reaction-based synthesis and biological evaluation of tricyclic heterofused quinolines with multi-trypanosomatid activity

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P5875

P698

P932