Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H11N |
| Molecular Weight | 229.2759 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1=CC2=C(C=C1)C3=NC4=CC=CC=C4C=C3C=C2
InChI
InChIKey=OAPPEBNXKAKQGS-UHFFFAOYSA-N
InChI=1S/C17H11N/c1-3-7-15-12(5-1)9-10-14-11-13-6-2-4-8-16(13)18-17(14)15/h1-11H
| Molecular Formula | C17H11N |
| Molecular Weight | 229.2759 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Base-base recognition of nonionic dinucleotide analogues in an apolar environment studied by low-temperature NMR spectroscopy. | 2010-03-24 |
|
| Assessment of azaarenes and azaarones (oxidized azaarene derivatives) in the Dutch coastal zone of the North Sea. | 2009-08 |
|
| Disposition of sanguinarine in the rat. | 2007-05 |
|
| Metabolism of sanguinarine: the facts and the myths. | 2007-02 |
|
| A liquid chromatographic-mass spectrometric evidence of dihydrosanguinarine as a first metabolite of sanguinarine transformation in rat. | 2006-01-02 |
|
| Aryl hydrocarbon receptor-mediated and estrogenic activities of oxygenated polycyclic aromatic hydrocarbons and azaarenes originally identified in extracts of river sediments. | 2001-12 |
|
| Phototoxicity of azaarene isomers to the marine flagellate Dunaliella tertiolecta. | 2001-07 |
|
| Surface changes and hormone production in pituitary cells during tumorigenesis. | 1999-12 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:45:41 GMT 2025
by
admin
on
Mon Mar 31 18:45:41 GMT 2025
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| Record UNII |
BV4376Y90X
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| Record Status |
Validated (UNII)
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| Record Version |
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9181
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225-51-4
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205-930-2
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89261
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C035985
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5094
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DTXSID9059759
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