(Q55113109)

English

Biosynthesis of rhodiocyanosides in Lotus japonicus: Rhodiocyanoside A is synthesized from (Z)-2-methylbutanaloxime via 2-methyl-2-butenenitrile

scientific article published in May 2012

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scholarly article

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Biosynthesis of rhodiocyanosides in Lotus japonicus: Rhodiocyanoside A is synthesized from (Z)-2-methylbutanaloxime via 2-methyl-2-butenenitrile (English)

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rhodiocyanoside A

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ChEBI release 2020-05-28

Lotus corniculatus

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2-Methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enenitrile

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2-[[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]but-2-enenitrile

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Rhodiocyanoside D

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2-(Hexopyranosyloxy)-2-methylbutanenitrile

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2(R)-Hydroxy-2-methylbutyronitrile-beta-D-glucopyranoside

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Lotus japonicus

object named as

Lotus japonicus

2 references

based on heuristic

inferred from title

Mohammed S Motawia

object named as

Mohammed Saddik Motawia

2

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object named as

Søren Bak

5

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Carl Erik Olsen

object named as

Carl Erik Olsen

3

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Birger Lindberg Møller

object named as

Birger Lindberg Møller

4

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author name string

Shigeki Saito

1

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publication date

May 2012

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77

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260-267

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Bioactive constituents of Chinese natural medicines. IV. Rhodiolae radix. (2).: On the histamine release inhibitors from the underground part of Rhodiola sacra (Prain ex Hamet) S. H. Fu (Crassulaceae): chemical structures of rhodiocyanoside D and sa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.45.1498

Bioactive constituents of Chinese natural medicines. II. Rhodiolae radix. (1). Chemical structures and antiallergic activity of rhodiocyanosides A and B from the underground part of Rhodiola quadrifida (Pall.) Fisch. et Mey. (Crassulaceae)

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.44.2086

The primary sequence of cytochrome P450tyr, the multifunctional N-hydroxylase catalyzing the conversion of L-tyrosine to p-hydroxyphenylacetaldehyde oxime in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench

1 reference

11 May 2024

https://opencitations.net/index/api/v1/citations/10.1006/ABBI.1995.0024

Identifiers

10.1016/J.PHYTOCHEM.2012.01.020

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