harmaline (Q104252234)

inferred from SMILES

chemical formula

C₁₃H₁₄N₂O

0 references

canonical SMILES

N1=C(C=2NC=3C=C(OC)C=CC3C2CC1)C

0 references

found in taxon

Peganum harmala

16 references

Isoharmine, a β-carboline alkaloid from Peganum harmala seeds

Chemical and biological investigation of harmal plant. 2. Alkaloidal investigation

New alkaloids from Peganum harmala

Trace analysis of harman alkaloids in passiflora incarnata by reversed-phase high performance liquid chromatography

Method for the quantitative determination of deoxypeganine from Peganum harmala

The dynamics of the accumulation of alkaloids in Peganum harmala

Lipids from the aerial part of Peganum harmala

Biosynthesis of serotonin and β-carboline alkaloids in hairy root cultures of Peganum harmala

Harmalidine, A β-carboline alkaloid from peganum harmala

An oxamide from Peganum harmala seeds

Antimicrobial Agents From Higher Plants. Antimicrobial Agents From Peganum harmala Seeds

The biogenesis of certain alkaloids

Hairy Root Cultures of Peganum harmala II. Characterization of Cell Lines and Effect of Culture Conditions on the Accumulation of ß-Carboline Alkaloids and Serotonin

An oxamide from Peganum harmala seeds

Alkaloids ofPeganum harmala

Antibacterial and antifungal activities of (beta)-carboline alkaloids of Peganum harmala (L) seeds and their combination effects.

Banisteriopsis caapi

3 references

Monoamine oxidase inhibitors in South American hallucinogenic plants: tryptamine and beta-carboline constituents of ayahuasca

Alkaloids of Banisteria caapi and Prestonia amazonicum

Banisteriopsis caapi, a unique combination of MAO inhibitory and antioxidative constituents for the activities relevant to neurodegenerative disorders and Parkinson's disease

Oxalis tuberosa

2 references

Exudation of fluorescent beta-carbolines from Oxalis tuberosa L roots

Exudation of fluorescent beta-carbolines from Oxalis tuberosa L roots

Passiflora actinia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora alata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora amethystina

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora ampullacea

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora boenderi

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora citrina

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora edulis

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora foetida

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora guatemalensis

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora helleri

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora incarnata

2 references

Trace analysis of harman alkaloids in passiflora incarnata by reversed-phase high performance liquid chromatography

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora jorullensis

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora laurifolia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora manicata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora menispermifolia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora multiflora

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora perfoliata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora phoenicia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora pilosicorona

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora racemosa

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora rubra

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora trisecta

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora tuberosa

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora princeps

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Identifiers

InChI

InChI=1S/C13H14N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-4,7,15H,5-6H2,1-2H3

0 references

0 references

CAS Registry Number

304-21-2

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

2 references

17 September 2022

ChEBI ID

28172

mapping relation type

exact match

2 references

ChEBI release 2021-03-01

International Chemical Identifier

InChI

InChI=1S/C13H14N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-4,7,15H,5-6H2,1-2H3

SureChEMBL ID

SCHEMBL199260

2 references

1 reference

NMRShiftDB structure ID

10018938

1 reference

DSSTox substance ID

DTXSID8041038

1 reference

DrugBank ID

DB13875

1 reference

Human Metabolome Database ID

HMDB0030310

2 references

KNApSAcK ID

C00001735

2 references

UNII

CN58I4TOET

1 reference