Alkaloids from the Sponge-Associated FungusAspergillussp

about

Co-cultivation--a powerful emerging tool for enhancing the chemical diversity of microorganisms Pretrichodermamides D-F from a Marine Algicolous Fungus Penicillium sp. KMM 4672.Simple indole alkaloids and those with a nonrearranged monoterpenoid unit Hot off the press

P2860

Q35096902-F0A2E272-9E94-4A94-8F7A-996DA8787578 Q38760985-3809FE65-CA21-4DEA-8226-FA9DB5F57012 Q58221062-277472EE-A65C-48E7-8609-28B31BEFF832 Q58856818-654E75DA-171B-4836-8DE5-E0FB2DFF84EA

P2860

Alkaloids from the Sponge-Associated FungusAspergillussp

Item

http://www.wikidata.org/entity/Q53606202

description

im Dezember 2012 veröffentlichter wissenschaftlicher Artikel

@de

wetenschappelijk artikel

@nl

наукова стаття, опублікована в грудні 2012

@uk

name

Alkaloids from the Sponge-Associated FungusAspergillussp

@en

Alkaloids from the Sponge-Associated FungusAspergillussp

@nl

type

Item

label

Alkaloids from the Sponge-Associated FungusAspergillussp

@en

Alkaloids from the Sponge-Associated FungusAspergillussp

@nl

prefLabel

Alkaloids from the Sponge-Associated FungusAspergillussp

@en

Alkaloids from the Sponge-Associated FungusAspergillussp

@nl

P1476

Alkaloids from the Sponge-Associated FungusAspergillussp

@en

P2093

Abdessamad Debbab

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

Amal H. Aly

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

Attila Mándi

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

Barbara Schulz

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

Matthias Kassack

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

Peter Proksch

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

Victor Wray

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

WenHan Lin

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

Werner E. G. Müller

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

Yaming Zhou

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

P2860

Properties of the K562 cell line, derived from a patient with chronic myeloid leukemia

Citrinin revisited: from monomers to dimers and beyond.

The odyssey of marine pharmaceuticals: a current pipeline perspective.

Fungal indole alkaloid biosynthesis: genetic and biochemical investigation of the tryptoquialanine pathway in Penicillium aethiopicum

Enzymatic processing of fumiquinazoline F: a tandem oxidative-acylation strategy for the generation of multicyclic scaffolds in fungal indole alkaloid biosynthesis.

New mono- and dimeric members of the secalonic acid family: blennolides A-G isolated from the fungus Blennoria sp.

Unraveling terminal C-domain-mediated condensation in fungal biosynthesis of imidazoindolone metabolites.

Natural products as sources of new drugs over the period 1981-2002.

The role of natural product chemistry in drug discovery.

Marine natural products of fungal origin.

P304

894-906

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

P31

scholarly article

P356

10.1002/EJOC.201201220

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

P433

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

P478

2013

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

P50

Tibor Kurtán

P577

2012-12-11T00:00:00Z

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

Alkaloids from the Sponge-Associated FungusAspergillussp

about

P2860

P2860

Alkaloids from the Sponge-Associated FungusAspergillussp

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577