(Q425157)

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

Linamarin structure.svg
620 × 355; 19 KB

1 reference

German Wikipedia

mass

247.105587 dalton

1 reference

LINAMARIN (English)

5 October 2016

C₁₀H₁₇NO₆

1 reference

LINAMARIN (English)

5 October 2016

CC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O

1 reference

LINAMARIN (English)

5 October 2016

CC(C)(C#N)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O

1 reference

Cyanogenic Glucosides In Linum Usitatissimum

LINAMARIN (English)

5 October 2016

6 references

Simultaneous extraction of oil and antinutritional compounds from flaxseed

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Cyanogenic compounds in flaxseed

Determination of Cyanogenic Glycosides in Flaxseed by Barbituric Acid−Pyridine, Pyridine−Pyrazolone, and High-Performance Liquid Chromatography Methods†

2 references

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

7 references

The biosynthesis of cyanogenic glucosides in seedlings of cassava (Manihot esculenta Crantz).

The biosynthesis of cyanogenic glucosides in roots of cassava

Cyanogenic and non-cyanogenic glycosides from Manihot esculenta

Cyanogenic Glycosides in Cassava, Manihot esculenta Crantz

On the Absence of 2-(2'-Cyclopentenyl)glycine-Derived Cyanogenic Glycosides in Cassava, Manihot esculenta Crantz

Biomarkers of tuber intake

Hevea brasiliensis

4 references

Changes in cyanogenic glucoside content in seeds and seedlings of Hevea species

Occurrence of lotaustralin in the genus Hevea and changes of HCN-potential in developing organs of Hevea brasiliensis

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

THE CYANOGENIC GLUCOSIDES AND GLUCOSIDASES OF RUBBER SEED KERNEL

Hevea benthamiana

2 references

Changes in cyanogenic glucoside content in seeds and seedlings of Hevea species

Occurrence of lotaustralin in the genus Hevea and changes of HCN-potential in developing organs of Hevea brasiliensis

Hevea pauciflora

2 references

Changes in cyanogenic glucoside content in seeds and seedlings of Hevea species

Occurrence of lotaustralin in the genus Hevea and changes of HCN-potential in developing organs of Hevea brasiliensis

Hevea spruceana

1 reference

Occurrence of lotaustralin in the genus Hevea and changes of HCN-potential in developing organs of Hevea brasiliensis

Hevea guianensis

1 reference

Occurrence of lotaustralin in the genus Hevea and changes of HCN-potential in developing organs of Hevea brasiliensis

Hevea camargoana

2 references

Changes in cyanogenic glucoside content in seeds and seedlings of Hevea species

Occurrence of lotaustralin in the genus Hevea and changes of HCN-potential in developing organs of Hevea brasiliensis

Acacia aroma

1 reference

Cyanogenic Glycosides from Four Latin American Species of Acacia

Lotus creticus

2 references

A coumestan from Lotus creticus

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Passiflora adenopoda

2 references

Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts

Linamarin, lotaustralin, linustatin and neolinustatin from Passiflora species

Passiflora foetida

2 references

Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts

Cyanogenesis of Passiflora foetida

Passiflora lutea

2 references

Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts

Co-occurrence of Valine/Isoleucine-derived and cyclopentenoid cyanogens in a Passiflora species

Passiflora morifolia

5 references

Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts

Cyanogenesis in Passifloraceae

Substrate specificity in the biosynthesis of cyclopentanoid cyanohydrin glucosides

Linamarin, lotaustralin, linustatin and neolinustatin from Passiflora species

Biosynthesis of cyanohydrin glucosides from unnatural nitriles in intact tissue of Passiflora morifolia and Turnera angustifolia

Passiflora pendens

2 references

Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts

Linamarin, lotaustralin, linustatin and neolinustatin from Passiflora species

Trifolium repens

5 references

Isolation of linamarin-lotaustralin from Trifolium repens

Determination of cyanogenic glucosides in white clover (Trifolium repens L.) by high performance liquid chromatography

Evidence that linamarin and lotaustralin, the two cyanogenic glucosides of Trifolium repens L., are synthesized by a single set of microsomal enzymes controlled by the Ac/ac locus

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Cyanotypic frequencies in adjacent and mixed populations of Trifolium occidentale Coombe and Trifolium repens L. are regulated by different mechanisms.

Linum grandiflorum

2 references

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

New acylated flavone and cyanogenic glycosides from Linum grandiflorum

Linum narbonense

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Lotus arabicus

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Lotus arenarius

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Lotus edulis

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Lotus maroccanus

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Lotus parviflorus

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Lotus tenuis

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Osteospermum ecklonis

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Dimorphotheca jucunda

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Osteospermum jucundum

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Passiflora subpeltata

1 reference

Cyanohydrin glycosides of passifloraceae☆

Turnera ulmifolia

1 reference

Biosynthesis of cyanohydrin glucosides from unnatural nitriles in intact tissue of Passiflora morifolia and Turnera angustifolia

Linum perenne

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Lotus corniculatus

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Trifolium occidentale

1 reference

Cyanotypic frequencies in adjacent and mixed populations of Trifolium occidentale Coombe and Trifolium repens L. are regulated by different mechanisms.

Lotus japonicus

1 reference

Genomic clustering of cyanogenic glucoside biosynthetic genes aids their identification inLotus japonicusand suggests the repeated evolution of this chemical defence pathway

1 reference

0 references

0 references

Linamarin

0 references

Identifiers

InChI

InChI=1S/C10H17NO6/c1-10(2,4-11)17-9-8(15)7(14)6(13)5(3-12)16-9/h5-9,12-15H,3H2,1-2H3/t5-,6-,7+,8-,9+/m1/s1

1 reference

LINAMARIN (English)

5 October 2016

2 references

LINAMARIN (English)

5 October 2016

ChEBI release 2020-09-01

CAS Registry Number

554-35-8

2 references

Global Substance Registration System

UNII

H3V9RP3WLO

LINAMARIN (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=554-35-8

10 April 2021

1 reference

Linamarin (English)

5 October 2016

2 references

English

LINAMARIN (English)

5 October 2016

ChEBI ID

16441

mapping relation type

2 references

English

linamarin (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C10H17NO6/c1-10(2,4-11)17-9-8(15)7(14)6(13)5(3-12)16-9/h5-9,12-15H,3H2,1-2H3/t5-,6-,7+,8-,9+/m1/s1

1 reference

LINAMARIN (English)

5 October 2016

2 references

inferred from InChIKey

splash10-014i-0950000000-e342877fd4dea6a86182

1 reference

0 references

splash10-0udi-0910000000-46fd8867749e9a54d5b7

0 references

splash10-0udi-0910000000-46e0422d451388f1ac6a

0 references

splash10-0006-0390000000-12125f39b36aef32a409

0 references

splash10-0006-0390000000-daf77877063e66cdc199

0 references

HSDB ID

3507

1 reference

Hazardous Substances Data Bank

28 October 2019

LINAMARIN (English)

10 May 2021

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

DTXCID5031268

0 references

EC number

637-249-5

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.164.971

27 December 2018

ECHA Substance Infocard ID

2-(beta-D-Glucopyranosyloxy)-2-methyl-propanenitrile (English)

quotation

CAS no.: 554-35-8 (English)

100.164.971

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.164.971

27 December 2018

Human Metabolome Database ID

2-(beta-D-Glucopyranosyloxy)-2-methyl-propanenitrile (English)

quotation

CAS no.: 554-35-8 (English)

HMDB0033699

2 references

based on heuristic

inferred from InChIKey

1 reference

Global Substance Registration System

linamarin (English)

5 October 2016

2 references

UNII

H3V9RP3WLO

English

LINAMARIN (English)

5 October 2016

0 references

1 reference

Great Russian Encyclopedia portal ID

1 reference

28 October 2013

linamarin-d12a16

0 references

Microsoft Academic ID

2777372874

0 references

Nikkaji ID

J6.462I

1 reference

Japanese Wikipedia

Römpp online ID

RD-12-01187

1 reference