(Q5862594)

Flindersine (English)

5 October 2016

chemical formula

C₁₄H₁₃NO₂

1 reference

Flindersine (English)

20 November 2016

canonical SMILES

CC1(C=CC2=C(O1)C3=CC=CC=C3NC2=O)C

1 reference

Microminutin, a novel cytotoxic coumarin from Micromelum minutum (Rutaceae)

Flindersine (English)

20 November 2016

1 reference

Zanthoxylum coco

2 references

Aurapten and Flindersine From Zanthoxylum coco

Fagara coco Gill. (Zanthoxylum coco Gill.)

Zanthoxylum heitzii

1 reference

Flindersine from Fagara heitzii

Haplophyllum acutifolium

12 references

Components of Haplophyllum perforatum

Haplophytin-A and B: the alkaloidal constituents of Haplophyllum acutifolium

Flindersine from Haplophyllum perforatum

Acetylhaplophyllidine, a new alkaloid fromHaplophyllum perforatum

Haplophytin-A and B: the alkaloidal constituents of Haplophyllum acutifolium

Alkaloids ofHaplophyllum perforatum

Flindersine from Haplophyllum perforatum

Components ofHaplophyllum acutifolium

Zanthoxylum chalybaeum

1 reference

Biocidal alkaloids from African Fagara plants: Inhibition of mitochondrial function.

Zanthoxylum chalybeum

1 reference

Biocidal alkaloids from African Fagara plants: Inhibition of mitochondrial function.

Haplophyllum tuberculatum

6 references

A new quinolone type alkaloid from haplophylum tuberculatum (rutaceae)

Alkaloids from Haplophyllum tuberculatum

Alkaloid, lignan and flavonoid constituents of Haplophyllum tuberculatum from Sudan

Alkaloids from Haplophyllum tuberculatum

New Alkaloids from Haplophyllum tuberculatum

Alkaloids from Haplophyllum tuberculatum

Zanthoxylum simulans

3 references

Novel Prenylated 2-Quinolinones from East AsianZanthoxylum Species

Chemical and anti-platelet constituents from Formosan Zanthoxylum simulans.

Chemical and anti-platelet constituents from Formosan Zanthoxylum simulans.

Haplophyllum suaveolens

2 references

Lignans and Alkaloids from Haplophyllum suaveolens

Alkaloids from Haplophyllum suaveolens

Glycosmis parviflora

1 reference

Stress induced carbazole phytoalexins in Glycosmis species

Helietta apiculata

1 reference

Quinoline alkaloids, coumarins and volatile constituents of Helietta longifoliata.

Haplophyllum bucharicum

2 references

Haplobucharine — A new alkaloid from Haplophyllum bucharicum

Components ofHaplophyllum bucharicum

Geijera balansae

1 reference

Plantes de Nouvelle-Calédonie, XCVI. Alcaloïdes de Geijera balansae

Haplophyllum

2 references

Dihydroperfamine, an alkaloid from haplophyllum glabrinum

Screening of 14 alkaloids isolated from Haplophyllum A. Juss. for their cytotoxic properties

Zanthoxylum beecheyanum

1 reference

Chemical and Antiplatelet Constituents from the Stem ofZanthoxylum Beecheyanum

Zanthoxylum zanthoxyloides

1 reference

Extractives from Fagara zanthoxyloides(Lam.)

Flindersia australis

1 reference

The chemical constituents of Australian Flindersia species. VI. The structure and chemisty of Flindersine

Zanthoxylum integrifoliolum

1 reference

Chemical Constituents from the Root Wood ofZanthoxylum Integrifoliolum

Zanthoxylum nitidum

1 reference

Secondary metabolites and cytotoxic activities from the stem bark of Zanthoxylum nitidum

Neoraputia paraensis

1 reference

Enzymatic inhibition studies of selected flavonoids and chemosystematic significance of polymethoxylated flavonoids and quinoline alkaloids in Neoraputia (Rutaceae)

Haplophyllum thesioides

1 reference

Alkaloids and Coumarins From Haplophyllum Thesioides

schematic

Biosíntesis de flindersina.png
820 × 349; 29 KB

0 references

Identifiers

InChI

InChI=1S/C14H13NO2/c1-14(2)8-7-10-12(17-14)9-5-3-4-6-11(9)15-13(10)16/h3-8H,1-2H3,(H,15,16)

1 reference

Flindersine (English)

20 November 2016

2 references

Flindersine (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

523-64-8

2 references

Global Substance Registration System

UNII

6A8PD12CKP

flindersine (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=523-64-8

10 April 2021

1 reference

Flindersine (English)

20 November 2016

2 references

Flindersine (English)

20 November 2016

ChEBI ID

5094

mapping relation type

2 references

FLINDERSINE (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C14H13NO2/c1-14(2)8-7-10-12(17-14)9-5-3-4-6-11(9)15-13(10)16/h3-8H,1-2H3,(H,15,16)

1 reference

MSBNK-Washington_State_Univ-BML01221

FLINDERSINE (English)

20 November 2016

1 reference

MassBank accession ID

0 references

MSBNK-Washington_State_Univ-BML01227

0 references

MSBNK-Washington_State_Univ-BML01233

0 references

MSBNK-Washington_State_Univ-BML01239

0 references

MSBNK-Washington_State_Univ-BML81240

0 references

MSBNK-Washington_State_Univ-BML81241

0 references

MSBNK-Washington_State_Univ-BML81242

0 references

MSBNK-Washington_State_Univ-BML81243

0 references

SPLASH

splash10-0209-0950000000-b8c2a87da3ef25e9c46c

0 references

splash10-014i-0900000000-655a8d8ece3c0c8faf73

0 references

splash10-004i-0090000000-4ce38ba0718a8fa0f0c9

0 references

splash10-004i-0090000000-6c7bbef53e0d4ee36cd3

0 references

splash10-004i-0090000000-46c4f09275aab6620531

0 references

splash10-004i-0090000000-3bed13b5851073622a23

0 references

NMRShiftDB structure ID

30001542

1 reference

DSSTox substance ID

DTXSID80200324

2 references

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

DSSTOX compound identifier

0 references

0 references

3 references

Flindersine (English)

5 October 2016

based on heuristic

inferred from InChIKey

UNII

6A8PD12CKP

2 references

Global Substance Registration System

UNII

6A8PD12CKP

flindersine (English)

20 November 2016

1 reference

Flindersine (English)