Tandem prenyltransferases catalyze isoprenoid elongation and complexity generation in biosynthesis of quinolone alkaloids.
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The 3,4-dioxygenated 5-hydroxy-4-aryl-quinolin-2(1H)-one alkaloids. Results of 20 years of research, uncovering a new family of natural products.Prenyltransferases as key enzymes in primary and secondary metabolism.Biosynthesis of fungal meroterpenoids.Lasiodiplactone A, a novel lactone from the mangrove endophytic fungus Lasiodiplodia theobromae ZJ-HQ1.Oxidative Cyclization in Natural Product BiosynthesisEnzyme-catalyzed cationic epoxide rearrangements in quinolone alkaloid biosynthesis.A convenient approach to an advanced intermediate toward the naturally occurring, bioactive 6-substituted 5-hydroxy-4-aryl-1H-quinolin-2-ones.Hot off the press
P2860
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P2860
Tandem prenyltransferases catalyze isoprenoid elongation and complexity generation in biosynthesis of quinolone alkaloids.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Tandem prenyltransferases cata ...... thesis of quinolone alkaloids.
@en
Tandem prenyltransferases cata ...... thesis of quinolone alkaloids.
@nl
type
label
Tandem prenyltransferases cata ...... thesis of quinolone alkaloids.
@en
Tandem prenyltransferases cata ...... thesis of quinolone alkaloids.
@nl
prefLabel
Tandem prenyltransferases cata ...... thesis of quinolone alkaloids.
@en
Tandem prenyltransferases cata ...... thesis of quinolone alkaloids.
@nl
P2093
P2860
P50
P356
P1476
Tandem prenyltransferases cata ...... thesis of quinolone alkaloids.
@en
P2093
Mancheng Tang
Ralph A Cacho
Zhajun Zhan
P2860
P304
P356
10.1021/JACS.5B03022
P407
P577
2015-04-14T00:00:00Z