Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

about

Merging chemical synthesis and biosynthesis: a new chapter in the total synthesis of natural products and natural product libraries.Aza-tryptamine substrates in monoterpene indole alkaloid biosynthesis.

P2860

Q37996334-E786F75C-DC4A-4070-85A2-B7456851B02B Q42936094-040A33A7-A4CF-49A3-AAEB-A52CCAB5AB0C

P2860

Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

Item

http://www.wikidata.org/entity/Q42571491

description

2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

2009年论文

@zh

2009年论文

@zh-cn

name

Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

@en

Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

@nl

type

Item

label

Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

@en

Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

@nl

prefLabel

Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

@en

Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

@nl

P1476

Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

@en

P2093

Nancy Yerkes

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

Peter Bernhardt

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

P2860

The structure of Rauvolfia serpentina strictosidine synthase is a novel six-bladed beta-propeller fold in plant proteins

Strictosidine synthase: mechanism of a Pictet-Spengler catalyzing enzyme

Molecular Architecture of Strictosidine Glucosidase: The Gateway to the Biosynthesis of the Monoterpenoid Indole Alkaloid Family

Molecular cloning and analysis of strictosidine beta-D-glucosidase, an enzyme in terpenoid indole alkaloid biosynthesis in Catharanthus roseus.

Inhibition of the alpha 1 and alpha 2-adrenoceptor-mediated pressor response in pithed rats by raubasine, tetrahydroalstonine and akuammigine.

The Catharanthus alkaloids: pharmacognosy and biotechnology.

Chemistry and biology of monoterpene indole alkaloid biosynthesis.

Substrate specificity and diastereoselectivity of strictosidine glucosidase, a key enzyme in monoterpene indole alkaloid biosynthesis.

Heterologous expression of a Rauvolfia cDNA encoding strictosidine glucosidase, a biosynthetic key to over 2000 monoterpenoid indole alkaloids.

Assessment of the therapeutic activity of a combination of almitrine and raubasine on functional rehabilitation following ischaemic stroke.

P304

4166-4168

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

P31

scholarly article

P356

10.1039/B916027M

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

P433

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

P478

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

P50

Sarah O'Connor

P577

2009-08-13T00:00:00Z

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

P5875

26861633

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

P698

19795053

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

P921

stereoselectivity

P932

3020909

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

Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

about

P2860

P2860

Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921

P932