1-hydroxy-3-methoxy-10-methylacridin-9-one (Q104193241)

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chemical compound

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Language	Label	Description	Also known as
English	1-hydroxy-3-methoxy-10-methylacridin-9-one	chemical compound

Statements

instance of

type of chemical entity

0 references

subclass of

acridone alkaloid

0 references

mass

255.089543276 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₁₅H₁₃NO₃

0 references

canonical SMILES

O=C1C=2C=CC=CC2N(C=3C=C(OC)C=C(O)C13)C

0 references

found in taxon

Conchocarpus marginatus

1 reference

stated in

Fitoquímica e quimiossistemática de Conchocarpus marginatus e C. inopinatus (Rutaceae)

Ruta graveolens

6 references

stated in

Fitoquímica e quimiossistemática de Conchocarpus marginatus e C. inopinatus (Rutaceae)

stated in

Acridone alkaloids of callus tissue ofRuta graveolens

stated in

Acridone alkaloids of callus tissue ofRuta graveolens

stated in

Acridin-Alkaloide aus Kalluskulturen von Ruta graveolens L. / Acridine-Alkaloids from Callus Cultures of Ruta graveolens L.

stated in

Furacridon, 1-hydroxy-3-methoxy-N-methylacridon und isogravacridonchlorin aus den wurzeln von Ruta graveolens

stated in

Alkaloids of the Australian Rutaceae: Acronychia baueri Schott. IV. Alkaloids present in the leaves

Zanthoxylum gilletii

1 reference

stated in

Antifeedant constituents from Fagara macrophylla

Esenbeckia pilocarpoides

1 reference

stated in

Alkaloids from Esenbeckia pilocarpoides

Zanthoxylum leprieurii

2 references

stated in

In vitro cytotoxic activity of isolated acridones alkaloids from Zanthoxylum leprieurii Guill. et Perr.

stated in

Constituents of Fagara macrophylla and Zanthoxylum rigidifolium Pericarps

Esenbeckia febrifuga

1 reference

stated in

In vitro antiplasmodial activity of extract and constituents from Esenbeckia febrifuga, a plant traditionally used to treat malaria in the Brazilian Amazon

Citrus grandis

1 reference

stated in

Antitumor-promoting activity of coumarins from citrus plants.

pomelo

1 reference

stated in

Antitumor-promoting activity of coumarins from citrus plants.

Zanthoxylum rubescens

1 reference

stated in

A note on the chloroform-soluble alkaloids of Eagara macrophylla.

Limonia acidissima

1 reference

stated in

Antimicrobial constituents from the stem bark of Feronia limonia.

Glycosmis pentaphylla

1 reference

stated in

Chemical constituents of Glycosmis arborea: three new carbazole alkaloids and their biological activity

Thamnosma montana

1 reference

stated in

Acridone Alkaloids from Cell Suspension Cultures of Thamnosma montana.

Vepris pilosa

1 reference

stated in

Alkaloids from the root bark of Vepris pilosa (author's transl)

Identifiers

InChI

InChI=1S/C15H13NO3/c1-16-11-6-4-3-5-10(11)15(18)14-12(16)7-9(19-2)8-13(14)17/h3-8,17H,1-2H3

0 references

InChIKey

OCUBFJMZYYIVBO-UHFFFAOYSA-N

0 references

CAS Registry Number

13161-83-6

1 reference

stated in

CAS (formerly Chemical Abstracts Service)

retrieved

25 January 2022

PubChem CID

5377412

2 references

stated in

PubChem

retrieved

17 September 2022

based on heuristic

inferred from InChIKey

matched by identifier from

InChIKey

InChIKey

OCUBFJMZYYIVBO-UHFFFAOYSA-N

ChEBI ID

173801

mapping relation type

exact match

2 references

stated in

ChEBI release 2022-06-13

matched by identifier from

International Chemical Identifier

InChI

InChI=1S/C15H13NO3/c1-16-11-6-4-3-5-10(11)15(18)14-12(16)7-9(19-2)8-13(14)17/h3-8,17H,1-2H3

UniChem compound ID

163608

1 reference

stated in

UniChem

Human Metabolome Database ID

HMDB0029322

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

InChIKey

InChIKey

OCUBFJMZYYIVBO-UHFFFAOYSA-N

KNApSAcK ID

C00024230

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

InChIKey

InChIKey

OCUBFJMZYYIVBO-UHFFFAOYSA-N

 

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