Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H11NO |
| Molecular Weight | 173.2111 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CCC2=C3N1CCC3=CC=C2
InChI
InChIKey=XRJLAOUDSILTFT-UHFFFAOYSA-N
InChI=1S/C11H11NO/c13-10-5-4-8-2-1-3-9-6-7-12(10)11(8)9/h1-3H,4-7H2
| Molecular Formula | C11H11NO |
| Molecular Weight | 173.2111 |
| 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 |
|---|---|---|
| Residue analysis of multi-class pesticides in watermelon by LC-MS/MS. | 2010-03 |
|
| Melanin is an essential component for the integrity of the cell wall of Aspergillus fumigatus conidia. | 2009-08-24 |
|
| Novel acetylcholinesterase inhibitor as increasing agent on rhythmic bladder contractions: SAR of 8-{3-[1-(3-fluorobenzyl)piperidin-4-yl]propanoyl}-1,2,5,6-tetrahydro-4H-pyrrolo[3,2,1-ij]quinolin-4-one (TAK-802) and related compounds. | 2005-03-15 |
|
| The role of melanin in the antagonistic interaction between the apple scab pathogen Venturia inaequalis and Microsphaeropsis ochracea. | 2002-04 |
|
| A structural account of substrate and inhibitor specificity differences between two naphthol reductases. | 2001-07-31 |
|
| Structures of trihydroxynaphthalene reductase-fungicide complexes: implications for structure-based design and catalysis. | 2001-01-10 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:38:01 GMT 2025
by
admin
on
Mon Mar 31 19:38:01 GMT 2025
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| Record UNII |
WS195Z0WJH
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| Record Status |
Validated (UNII)
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| Record Version |
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