A multicomponent macrocyclization strategy to natural product-like cyclic lipopeptides: synthesis and anticancer evaluation of surfactin and mycosubtilin analogues.

about

A multicomponent macrocyclization strategy to natural product-like cyclic lipopeptides: synthesis and anticancer evaluation of surfactin and mycosubtilin analogues.

Item

http://www.wikidata.org/entity/Q36345731

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

A multicomponent macrocyclizat ...... in and mycosubtilin analogues.

@ast

A multicomponent macrocyclizat ...... in and mycosubtilin analogues.

@en

type

Item

label

A multicomponent macrocyclizat ...... in and mycosubtilin analogues.

@ast

A multicomponent macrocyclizat ...... in and mycosubtilin analogues.

@en

prefLabel

A multicomponent macrocyclizat ...... in and mycosubtilin analogues.

@ast

A multicomponent macrocyclizat ...... in and mycosubtilin analogues.

@en

P1476

A multicomponent macrocyclizat ...... tin and mycosubtilin analogues

@en

P2093

Alfredo R Puentes

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

Ali N Hmedat

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

Annegret Laub

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

Anselmo J Otero-González

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

Micjel C Morejón

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

P2860

Structure and dynamics of surfactin studied by NMR in micellar media

Detergent-like action of the antibiotic peptide surfactin on lipid membranes.

Solution- and Solid-Phase Macrocyclization of Peptides by the Ugi-Smiles Multicomponent Reaction: Synthesis of N-Aryl-Bridged Cyclic Lipopeptides.

Versatile antitumor potential of isoxanthohumol: Enhancement of paclitaxel activity in vivo.

Improved in vitro antitumor potential of (O,O'-Diisobutyl-ethylenediamine-N,N'-di-3-propionate)tetrachloridoplatinum(IV) complex under normoxic and hypoxic conditions.

Consecutive isocyanide-based multicomponent reactions: synthesis of cyclic pentadepsipeptoids.

Systematic conformational investigations of peptoids and peptoid-peptide chimeras.

Multiple multicomponent macrocyclizations (MiBs): a strategic development toward macrocycle diversity.

Multiple multicomponent macrocyclizations including bifunctional building blocks (MiBs) based on Staudinger and Passerini three-component reactions.

Diversity oriented one-pot synthesis of complex macrocycles: very large steroid-peptoid hybrids from multiple multicomponent reactions including bifunctional building blocks.

P304

3628-3637

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

P31

scholarly article

P356

10.1039/C7OB00459A

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

P433

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

P478

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

P50

Goran N Kaluđerović

Ludger A Wessjohann

Daniel G Rivera

P577

2017-05-01T00:00:00Z

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

P698

28406518

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