rutecarpine (Q15424771)

Rutaecarpine (English)

5 October 2016

chemical formula

C₁₈H₁₃N₃O

1 reference

Rutaecarpine (English)

18 November 2016

canonical SMILES

C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4

1 reference

Isolation of secondary metabolites from Hortia oreadica (Rutaceae) leaves through high-speed counter-current chromatography

Rutaecarpine (English)

18 November 2016

2 references

The Alkaloids of Hortia arborea Engl.1

Hortia badinii

1 reference

Isolation of secondary metabolites from Hortia oreadica (Rutaceae) leaves through high-speed counter-current chromatography

Euodia rutaecarpa

11 references

Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968

Determination of the alkaloids in Evodiae Fructus by high-performance liquid chromatography

Mechanism of inhibition of platelet aggregation by rutaecarpine, an alkaloid isolated from Evodia rutaecarpa

Determination of the alkaloids in Evodiae fructus by capillary electrophoresis

Uterotonic effect of Evodia rutaecarpa alkaloids

Two 5-HT1AReceptor-Interactive Tryptamine Derivatives from the Unripe Fruit ofEvodiarutaecarpa

Antinociceptive activities of 70% methanol extract of evodiae fructus (fruit of Evodia rutaecarpa var. bodinieri) and its alkaloidal components

Antianoxic action and active constituents of evodiae fructus

[A simultaneous determination of evodiamine and rutaecarpine in oriental pharmaceutical decoctions containing Evodia fruit by ion-pair high-performance liquid chromatography]

Two New Indoloquinazoline Alkaloids from the Unripe Fruits of Evodia rutaecarpa

Indoloquinazoline alkaloids from Euodia rutaecarpa and their cytotoxic activities

Tetradium ruticarpum

7 references

On the Evaluation of the Preparation of Chinese Medicinal Prescriptions. VI. The Changes of the Alkaloid Contents by Processing of Evodia Fruit

Quinoline alkaloids from the fruits of Evodia officinalis

7-Hydroxyrutaecarpine from Tetradium glabrifolium and Tetradium ruticarpum

A new quinolone and other constituents from the fruits of Tetradium ruticarpum: effects on neutrophil pro-inflammatory responses

7-Hydroxyrutaecarpine from Tetradium glabrifolium and Tetradium ruticarpum

Induction of NAD(P)H: quinone reductase by rutaecarpine isolated from the fruits of Evodia rutaecarpa in the murine hepatic Hepa-1c1c7 cell line

Quantitative analyses of indoloquinazoline alkaloids in Fructus Evodiae by high-performance liquid chromatography with atmospheric pressure chemical ionization tandem mass spectrometry

Zanthoxylum wutaiense

2 references

Constituents of the root wood of Zanthoxylum wutaiense with antitubercular activity

Indolopyridoquinazoline alkaloids with antiplatelet aggregation activity from Zanthoxylum integrifoliolum

Tetradium glabrifolium

2 references

The heartwood constituents of Tetradium glabrifolium

Constituents of Leaves of Tetradium Glabrifolium

Bouchardatia neurococca

2 references

Alkaloids and limonoids from Bouchardatia neurococca: systematic significance

Alkaloids and Limonoids from Bouchardatia neurococca: Systematic Significance.

Zanthoxylum integrifoliolum

5 references

Indolopyridoquinazoline alkaloids with antiplatelet aggregation activity from Zanthoxylum integrifoliolum

Chemical Constituents from the Root Wood ofZanthoxylum Integrifoliolum

Chemical constituents and biological activities of the fruit of Zanthoxylum integrifoliolum

New indolopyridoquinazoline, benzo[c]phenanthridines and cytotoxic constituents from Zanthoxylum integrifoliolum

Constituents of the root wood of Zanthoxylum wutaiense with antitubercular activity

Phellodendron amurense

3 references

Indolopyridoquinazoline, furoquinoline and canthinone type alkaloids from Phellodendron amurense callus tissues

A new indolopyridoquinazoline-type alkaloid from phellodendron amurense callus tissues

Constituents of leaves of Phellodendron japonicum MAXIM. and their antioxidant activity

Hortia regia

1 reference

Constituents of Hortia regia: 6,7-Dimethoxycoumarin, Rutaecarpine, Skimmianine, and (+)-Methyl (E,E)-10,11-Dihydroxy-3,7,11-Trimethyl-2,6-Dodecadienoate

Zanthoxylum budrunga

1 reference

Occurrence of Rutaecarpine in Zanthoxylum budrunga

Spiranthera odoratissima

1 reference

New limonoids from Hortia oreadica and unexpected coumarin from H. superba using chromatography over cleaning Sephadex with sodium hypochlorite.

Zanthoxylum dimorphophyllum

1 reference

Cytotoxic Constituents from the Stem Bark ofZanthoxylum Pistaciiflorum

Phellodendron chinense

4 references

Identification and analysis of alkaloids in cortex Phellodendron amurense by high-performance liquid chromatography with electrospray ionization mass spectrometry coupled with photodiode array detection

Indolopyridoquinazoline, furoquinoline and canthinone type alkaloids from Phellodendron amurense callus tissues

Constituents of leaves of Phellodendron japonicum MAXIM. and their antioxidant activity

A new indolopyridoquinazoline-type alkaloid from phellodendron amurense callus tissues

Zanthoxylum integrifolium

1 reference

Chemical constituents and biological activities of the fruit of Zanthoxylum integrifoliolum

Zanthoxylum rhetsa

4 references

Occurrence of Rutaecarpine in Zanthoxylum budrunga

Indonesian Medicinal Plants. IV. On the Constituents of the Bark of Fagara rhetza (Rutaceae). (2). Lignan Glycosides and Two Apioglucosides.

Indonesia medicinal plants. III. On the constituents of the bark of Fagara rhetza (Rutaceae). (1): Alkaloids, phenylpropanoids, and acid amide

Chemical Study of Indonesian Medicinal Plants

subject has role

vasodilator agent

1 reference

InChI=1S/C18H13N3O/c22-18-13-6-2-4-8-15(13)20-17-16-12(9-10-21(17)18)11-5-1-3-7-14(11)19-16/h1-8,19H,9-10H2

Medical Subject Headings

15 March 2018

0 references

Identifiers

InChI

1 reference

Rutaecarpine (English)

18 November 2016

2 references

Rutaecarpine (English)

18 November 2016

ChEBI release 2020-09-01

CAS Registry Number

84-26-4

2 references

Global Substance Registration System

UNII

8XZV289PRY

rutecarpine (English)

18 November 2016

https://commonchemistry.cas.org/detail?cas_rn=84-26-4

10 April 2021

1 reference

Rutaecarpine (English)

18 November 2016

2 references

Rutaecarpine (English)

18 November 2016

ChEBI ID

8922

mapping relation type

2 references

RUTAECARPINE (English)

18 November 2016

International Chemical Identifier

InChI

InChI=1S/C18H13N3O/c22-18-13-6-2-4-8-15(13)20-17-16-12(9-10-21(17)18)11-5-1-3-7-14(11)19-16/h1-8,19H,9-10H2

1 reference

RUTAECARPINE (English)

18 November 2016

2 references

inferred from InChIKey

splash10-03ri-0090000000-8f0a0f5423af8441df1f

1 reference

0 references

NMRShiftDB structure ID

20123167

1 reference

DSSTox substance ID

DTXSID00232884

2 references

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

DSSTOX compound identifier

0 references

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Rutacarpin (English)

CAS no.: 84-26-4 (English)

ECHA Substance Infocard ID

100.163.752

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Rutacarpin (English)

CAS no.: 84-26-4 (English)

MeSH descriptor ID

C028632

1 reference

Medical Subject Headings

MeSH descriptor ID

C028632

Human Metabolome Database ID

14 March 2018

HMDB0042010

2 references

based on heuristic

inferred from InChIKey

3 references

Rutecarpine (English)

5 October 2016

based on heuristic

inferred from InChIKey

UNII

8XZV289PRY

2 references

Global Substance Registration System

UNII

8XZV289PRY

rutecarpine (English)

18 November 2016

0 references

1 reference

https://docs.openalex.org/download-snapshot/snapshot-data-format

Rutecarpine (English)

5 October 2016

0 references

1 reference

26 January 2022

UMLS CUI

C0073716

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023