(Q414226)

9H-Pyrido[3,4-B]indole (English)

19 October 2016

chemical formula

C₁₁H₈N₂

1 reference

9H-Pyrido[3,4-B]indole (English)

20 November 2016

canonical SMILES

C1=CC=C2C(=C1)C3=C(N2)C=NC=C3

1 reference

Recon 2.2: from reconstruction to model of human metabolism

9H-Pyrido[3,4-B]indole (English)

20 November 2016

2 references

A community-driven global reconstruction of human metabolism.

Prunus dulcis

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Cashew

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Polygala tenuifolia

2 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

β-Carboline alkaloids ofPolygala tenuifolia

Passiflora incarnata

2 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Juglans regia

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Pinellia ternata

2 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Areca catechu

2 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Great yellow gentian

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Tribulus terrestris

3 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Locomotor effects in sheep of alkaloids identified in Australian Tribulus terrestris

Tedania anhelans

1 reference

Secondary Metabolites from the SpongeTedaniaanhelans: Isolation and Characterization of Two Novel Pyrazole Acids and Other Metabolites

Acraea andromacha

1 reference

High-performance liquid chromatographic identification of simple β-carboline alkaloids in specimens of heliconiini butterflies

Ailanthus altissima

1 reference

Studies on the constituents of Ailanthus altissima SWINGLE. III. The alkaloidal constituents.

Ailanthus triphysa

1 reference

Alkaloids and quassinoids from Ailanthus malabarica

Brucea mollis

1 reference

Alkaloids and quassinoids of Brucea mollis var. tonkinensis

Bupleurum falcatum

1 reference

Chroococcus minutus

1 reference

Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth.

Commelina communis

1 reference

Anticariogenic β-carboline alkaloids fromCommelina communis

Cribricellina cribraria

1 reference

New cytotoxic beta-carboline alkaloids from the marine bryozoan, Cribricellina cribraria

Didemnum

1 reference

Didemnolines A-D, new N9-substituted β-carbolines from the marine ascidian Didemnum sp.

Euodia rutaecarpa

1 reference

Eurycoma harmandiana

1 reference

Canthin-6-one and beta-carboline alkaloids from Eurycoma harmandiana

Eurycoma longifolia

4 references

Cytotoxic and Antimalarial β-Carboline Alkaloids from the Roots of Eurycoma longifolia

Canthin-6-one alkaloids from Eurycoma longifolia

Cytotoxic and antimalarial constituents of the roots of Eurycoma longifolia

Eurycomaoside: A New Quassinoid-Type Glycoside from the Roots of Eurycoma longifolia.

Gentiana

1 reference

Isatis tinctoria

1 reference

Acid constituents from Isatis tinctoria

Nicotiana tabacum

1 reference

The isolation of harmane and norharmane from tobacco and cigarette smoke

Nocardia

1 reference

Isolation of harman and norharman from Nocardia sp. and their inhibitory activity against plant seedlings.

Nodularia harveyana

2 references

Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth.

Screening of microalgal culture media for the presence of algicidal compounds and isolation and identification of two bioactive metabolites, excreted by the cyanobacteria Nostoc insulare and Nodularia harveyana

Nostoc carneum

1 reference

Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth.

Nostoc commune

1 reference

Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth.

Ophiopogon

1 reference

Panax ginseng

3 references

A thiazole and two β-carboline constitutents fromPanax ginseng

Alkaloidal components ofPanax ginseng

Picrasma quassioides

1 reference

Studies on the constituents of Picrasma quassioides BENNET. III. The alkaloidal constituents.

Polygala

1 reference

Quassia africana

1 reference

Indole Alkaloids and Quassin from Quassia africana

Rauvolfia serpentina

1 reference

Isolation of Alkaloids from Cultured Hybrid Cells of Rauwolfia serpentina*Rhazya stricta.

Rauvolfia sumatrana

1 reference

Novel Indole Alkaloids from the Leaves of Rauwolfia sumatrana JACK. in Thailand.

Ritterella sigillinoides

1 reference

Eudistomins From the New Zealand AscidianRitterella sigillinoides

Schisandra chinensis

1 reference

Senecio leptolobus

1 reference

Pyrrolizidine alkaloid composition in six brazilian Senecio species

Strychnos johnsonii

1 reference

Alkaloids of Strychnos johnsonii

Strychnos potatorum

1 reference

Alkaloids from roots of Strychnos potatorum

Synechocystis aquatilis

1 reference

Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth.

Tetradium glabrifolium

1 reference

Constituents of Leaves of Tetradium Glabrifolium

Zingiber officinale

1 reference

Trametes maxima

1 reference

Monoamine oxidase inhibitors isolated from fermented broths

Streptomyces nigra

4 references

Antioxidative Potential of a Streptomyces sp. MUM292 Isolated from Mangrove Soil.

Streptomyces nigra sp. nov. Is a Novel Actinobacterium Isolated From Mangrove Soil and Exerts a Potent Antitumor Activity in Vitro

Streptomyces sp. MUM273b: A mangrove-derived potential source for antioxidant and UVB radiation protectants

Antimicrobial Lavandulylated Flavonoids from a Sponge-Derived Streptomyces sp. G248 in East Vietnam Sea

Noctiluca miliaris

1 reference

TRACE CHARACTERIZATION OF THE FLUORESCENT SUBSTANCES OF A DINOFLAGELLATE,NOCTILUCA MILIARIS

Noctiluca scintillans

1 reference

TRACE CHARACTERIZATION OF THE FLUORESCENT SUBSTANCES OF A DINOFLAGELLATE,NOCTILUCA MILIARIS

Ophiorrhiza acuminata

1 reference

Glucoindole alkaloids from Ophiorrhiza acuminata

Scopolia

1 reference

The fluorescence of scorpions and cataractogenesis

Striped bark scorpion

1 reference

1 reference

The fluorescence of scorpions and cataractogenesis

Arthrospira laxissima

1 reference

Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth.

Catharanthus roseus

1 reference

EXPLORING ANTI-HYPERGLYCEMIC POTENTIAL OF ALKALOID COMPOUNDS FROM CATHARANTHUS ROSEUS G. DON (L) AGAINST VARIOUS TYPE II DIABETES TARGETS BY IN SILICO VIRTUAL SCREENING

Paracribricellina cribraria

1 reference

New cytotoxic beta-carboline alkaloids from the marine bryozoan, Cribricellina cribraria

Prunus avium

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

physically interacts with

Indoleamine 2,3-dioxygenase 1

subject has role

enzyme inhibitor

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

8222

InChI=1S/C11H8N2/c1-2-4-10-8(3-1)9-5-6-12-7-11(9)13-10/h1-7,13H

17 August 2016

1 reference

Medical Subject Headings

15 March 2018

1 reference

Medical Subject Headings

15 March 2018

0 references

0 references

0 references

Carbolines

1 reference

inferred from

Category:Beta-Carbolines

topic's main category

Category:Beta-Carbolines

0 references

Identifiers

InChI

1 reference

9H-Pyrido[3,4-B]indole (English)

AIFRHYZBTHREPW-UHFFFAOYSA-N

20 November 2016

InChIKey

2 references

9H-Pyrido[3,4-B]indole (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

244-63-3

2 references

Global Substance Registration System

AIFRHYZBTHREPW-UHFFFAOYSA-N

norharman (English)

20 November 2016

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=244-63-3

1 reference

norhaman (English)

20 November 2016

1 reference

9H-Pyrido[3,4-B]indole (English)

20 November 2016

Reaxys registry number

128414

1 reference

beta-carboline (English)

19 October 2016

ChEBI ID

109895

mapping relation type

1 reference

NORHARMANE (English)

20 November 2016

1 reference

MSBNK-Fac_Eng_Univ_Tokyo-JP000785

NORHARMANE (English)

20 November 2016

1 reference

MassBank accession ID

0 references

MSBNK-UFZ-UA007501

0 references

MSBNK-IPB_Halle-PB003761

0 references

SPLASH

splash10-014i-0900000000-5f1c82b770634430089f

0 references

DSSTox substance ID

DTXSID2021070

1 reference

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

DSSTOX compound identifier

0 references

0 references

205-959-0

1 reference

Global Substance Registration System

norharman (English)

ECHA Substance Infocard ID

20 November 2016

100.005.418

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.005.418

27 December 2018

Guide to Pharmacology Ligand ID

9H-pyrido[3,4-b]indole (English)

quotation

CAS no.: 244-63-3 (English)

1 reference

8222

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

8222

beta-carboline (English)

20 November 2016

1 reference

Medical Subject Headings

MeSH descriptor ID

C010262

Human Metabolome Database ID

14 March 2018

HMDB0012897

1 reference

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00026537

1 reference

based on heuristic

inferred from InChIKey

1 reference

Global Substance Registration System

norharman (English)

20 November 2016

Natural Product Atlas ID

NPA007873

1 reference

based on heuristic

inferred from InChIKey

0 references

1 reference

Immune Epitope Database and Analysis Resource

beta-carboline (English)

19 October 2016

1 reference

1 March 2022

0 references

1 reference

28 October 2013

1 reference

9 July 2020

Microsoft Academic ID

2778705115

0 references

Nikkaji ID

J10.931B

1 reference

imported from Wikimedia project

Japanese Wikipedia

Wikimedia import URL

https://ja.wikipedia.org/w/index.php?title=Β-カルボリン&oldid=67481140

1 reference

4K9I (English)