(Q5368476)

ELYMOCLAVINE (English)

5 October 2016

chemical formula

C₁₆H₁₈N₂O

1 reference

ELYMOCLAVINE (English)

19 November 2016

canonical SMILES

CN1CC(=CC2C1CC3=CNC4=CC=CC2=C34)CO

1 reference

ELYMOCLAVINE (English)

19 November 2016

isomeric SMILES

CN1CC(=C[C@H]2[C@H]1CC3=CNC4=CC=CC2=C34)CO

1 reference

Psychotomimetic Ergot Alkaloid Contents of Seed from Calonyction muricatum, Jacquemontia tamnifolia, Quamoclit lobata, and Q. sloteri

ELYMOCLAVINE (English)

19 November 2016

1 reference

Jacquemontia tamnifolia

1 reference

Psychotomimetic Ergot Alkaloid Contents of Seed from Calonyction muricatum, Jacquemontia tamnifolia, Quamoclit lobata, and Q. sloteri

Balansia strangulans

1 reference

Ergot alkaloid identification in clavicipitaceae systemic fungi of pasture grasses

Balansia epichloe

2 references

Ergot alkaloid identification in clavicipitaceae systemic fungi of pasture grasses

Lysergic Acid Amide Derivatives From Balansia epichloë and Balansia claviceps (Clavicipitaceae)

Epichloe typhina

1 reference

Ergot alkaloid identification in clavicipitaceae systemic fungi of pasture grasses

Ipomoea corymbosa

1 reference

Resin glycosides from Ipomoea pes-caprae

Turbina corymbosa

1 reference

Resin glycosides from Ipomoea pes-caprae

Ergot

6 references

Probing ergot alkaloid biosynthesis: intermediates in the formation of ring C

Stereochemistry of the isoprenylation of tryptophan catalyzed by 4-(.gamma.,.gamma.-dimethylallyl)tryptophan synthase from Claviceps, the first pathway-specific enzyme in ergot alkaloid biosynthesis

Probing ergot alkaloid biosynthesis: identification of advanced intermediates along the biosynthetic pathway

Biosynthesis of ergot alkaloids: origin of the oxygen atoms in chanoclavine-I and elymoclavine

End-Product Regulation of Ergot Alkaloid Formation in Intact Cells and Protoplasts of Claviceps Species, Strain SD 58

Biosynthesis of Ergot Alkaloids. Incorporation of (17R)-[17-3H]- and (17S)-[17-3H] Chanoclavine-I Into Elymoclavine by Claviceps

Claviceps purpurea

2 references

Steric course of the N-methylation in the biosynthesis of ergot alkaloids by Claviceps purpurea

Degradation Products of Ergot Alkaloids

Ipomoea hederacea

1 reference

ERGOT ALKALOID CONTENTS OF Ipomoea lacunosa, I. hederaceae, I. trichocarpa, AND I. purpurea SEED

Ipomoea lacunosa

1 reference

ERGOT ALKALOID CONTENTS OF Ipomoea lacunosa, I. hederaceae, I. trichocarpa, AND I. purpurea SEED

Ipomoea purpurea

1 reference

ERGOT ALKALOID CONTENTS OF Ipomoea lacunosa, I. hederaceae, I. trichocarpa, AND I. purpurea SEED

Securidaca longepedunculata

1 reference

Indole alkaloids from the roots of an african plantsecuridaca longipedunculata.I. Isolation by column chromatography and preliminary structural characterization by mass spectrometry

Ipomoea violacea

2 references

ERGOT ALKALOID CONTENTS OF Ipomoea lacunosa, I. hederaceae, I. trichocarpa, AND I. purpurea SEED

1 reference

Psychotomimetic Ergot Alkaloid Contents of Seed from Calonyction muricatum, Jacquemontia tamnifolia, Quamoclit lobata, and Q. sloteri

Ipomoea lobata

1 reference

Psychotomimetic Ergot Alkaloid Contents of Seed from Calonyction muricatum, Jacquemontia tamnifolia, Quamoclit lobata, and Q. sloteri

Ipomoea capillacea

1 reference

Psychotomimetic Ergot Alkaloid Contents of Seed from Calonyction muricatum, Jacquemontia tamnifolia, Quamoclit lobata, and Q. sloteri

Ipomoea tricolor

1 reference

InChI=1S/C16H18N2O/c1-18-8-10(9-19)5-13-12-3-2-4-14-16(12)11(7-17-14)6-15(13)18/h2-5,7,13,15,17,19H,6,8-9H2,1H3/t13-,15-/m1/s1

Ergot Alkaloids

Identifiers

InChI

1 reference

ELYMOCLAVINE (English)

19 November 2016

2 references

ELYMOCLAVINE (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

548-43-6

2 references

Global Substance Registration System

UNII

5LR46DLO0D

elymoclavine (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=548-43-6

10 April 2021

1 reference

8,9-Didehydro-6-methylergoline-8-methanol (English)

19 November 2016

2 references

ELYMOCLAVINE (English)

19 November 2016

ChEBI ID

4777

mapping relation type

2 references

Elymoclavine (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C16H18N2O/c1-18-8-10(9-19)5-13-12-3-2-4-14-16(12)11(7-17-14)6-15(13)18/h2-5,7,13,15,17,19H,6,8-9H2,1H3/t13-,15-/m1/s1

1 reference

CHEMBL3706997 (English)

19 November 2016

1 reference

1 reference

DSSTOX compound identifier

0 references

0 references

208-948-9

1 reference

Global Substance Registration System

UNII

5LR46DLO0D

elymoclavine (English)

ECHA Substance Infocard ID

19 November 2016

100.008.136

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.008.136

27 December 2018

reason for deprecated rank

Elymoclavine (English)

quotation

CAS no.: 548-43-6 (English)

KNApSAcK ID

C00001717

cannot be confirmed by other sources

1 reference

Global Substance Registration System

Elymoclavine (English)

5 October 2016

2 references

UNII

5LR46DLO0D

elymoclavine (English)

19 November 2016

1 reference

Elymoclavine (English)