lotaustralin (Q905492)

Lotaustralin (English)

2-(Hexopyranosyloxy)-2-methylbutanenitrile

5 October 2016

stereoisomer of

1 reference

based on heuristic

inferred from InChI

(2R)-2-methyl-2-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanenitrile

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₁H₁₉NO₆

1 reference

Lotaustralin (English)

20 November 2016

canonical SMILES

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

1 reference

Lotaustralin (English)

20 November 2016

isomeric SMILES

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

1 reference

Cyanogenic Glycosides from Four Latin American Species of Acacia

Lotaustralin (English)

20 November 2016

1 reference

Berberidopsis beckleri

1 reference

Occurrence of lotaustralin in Berberidopsis beckleri and its relation to the chemical evolution of flacourtiaceae

Euphorbia hirta

1 reference

Hirtionosides A-C, gallates of megastigmane glucosides, 3-hydroxyoctanoic acid glucosides and a phenylpropanoid glucoside from the whole plants of Euphorbia hirta

Euphorbia maculata

1 reference

Supinaionosides A and B: megastigmane glucosides and supinanitrilosides A-F: hydroxynitrile glucosides from the whole plants of Euphorbia supina RAFINESQUE

Euphorbia supina

1 reference

Supinaionosides A and B: megastigmane glucosides and supinanitrilosides A-F: hydroxynitrile glucosides from the whole plants of Euphorbia supina RAFINESQUE

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 brasiliensis

2 references

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

THE CYANOGENIC GLUCOSIDES AND GLUCOSIDASES OF RUBBER SEED KERNEL

Hevea camargoana

1 reference

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

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

Linum grandiflorum

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Linum narbonense

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Linum usitatissimum

4 references

Cyanogenic Glucosides In Linum Usitatissimum

Q104252650

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Cyanogenic Glucosides In Linum Usitatissimum

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 corniculatus

1 reference

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Lotus creticus

2 references

A coumestan from Lotus creticus

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

Manihot Esculenta

4 references

Cyanogenic and non-cyanogenic glycosides from Manihot esculenta

Cyanogenic Glycosides in Cassava, Manihot esculenta Crantz

Q104252650

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

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 adenopoda

1 reference

Linamarin, lotaustralin, linustatin and neolinustatin from Passiflora species

Passiflora lutea

1 reference

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

Passiflora pendens

1 reference

Linamarin, lotaustralin, linustatin and neolinustatin from Passiflora species

2 references

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

Rhodiola sachalinensis

1 reference

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

Trifolium repens

4 references

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

The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants

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

Linum perenne

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.

Caenorhabditis elegans

1 reference

Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism

Rhodiola rosea

2 references

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

Lotaustralin from Rhodiola rosea roots

0 references

0 references

Lotaustralin

0 references

Identifiers

InChI

InChI=1S/C11H19NO6/c1-3-11(2,5-12)18-10-9(16)8(15)7(14)6(4-13)17-10/h6-10,13-16H,3-4H2,1-2H3/t6-,7-,8+,9-,10+,11-/m1/s1

1 reference

Lotaustralin (English)

20 November 2016

2 references

Lotaustralin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

534-67-8

2 references

Global Substance Registration System

UNII

P588137A94

lotaustralin (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=534-67-8

9 April 2021

1 reference

Lotaustralin (English)

20 November 2016

2 references

Lotaustralin (English)

20 November 2016

ChEBI ID

6542

mapping relation type

2 references

Lotaustralin (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C11H19NO6/c1-3-11(2,5-12)18-10-9(16)8(15)7(14)6(4-13)17-10/h6-10,13-16H,3-4H2,1-2H3/t6-,7-,8+,9-,10+,11-/m1/s1

SureChEMBL ID

SCHEMBL42924

2 references

based on heuristic

inferred from InChIKey

1 reference

1 reference

DSSTOX compound identifier

0 references

1 reference

Global Substance Registration System

Lotaustralin (English)

5 October 2016

2 references

UNII

P588137A94

lotaustralin (English)

20 November 2016

1 reference