Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H7NO |
| Molecular Weight | 133.1473 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC2=C(C=CN2)C=C1
InChI
InChIKey=XAWPKHNOFIWWNZ-UHFFFAOYSA-N
InChI=1S/C8H7NO/c10-7-2-1-6-3-4-9-8(6)5-7/h1-5,9-10H
| Molecular Formula | C8H7NO |
| Molecular Weight | 133.1473 |
| 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 |
|---|---|---|
| N-(3,5-dihydroxybenzoyl)-6-hydroxytryptamine as a novel human tyrosinase inhibitor that inactivates the enzyme in cooperation with l-3,4-dihydroxyphenylalanine. | 2010-11 |
|
| Inhibitory effect of hydroxyindoles and their analogues on human melanoma tyrosinase. | 2010-04-02 |
|
| Bicyclic compounds repress membrane vesicle production and Pseudomonas quinolone signal synthesis in Pseudomonas aeruginosa. | 2010-03 |
|
| Monoindole alkaloids from a marine sponge Spongosorites sp. | 2007-06-25 |
|
| Hyrtioerectines A-C, cytotoxic alkaloids from the red sea sponge hyrtioserectus. | 2005-09 |
|
| A facile preparation of 1-(6-hydroxyindol-1-yl)-2,2-dimethylpropan-1-one. | 2003-01 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:20:12 GMT 2025
by
admin
on
Mon Mar 31 19:20:12 GMT 2025
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| Record UNII |
3I03JZ599T
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| Record Status |
Validated (UNII)
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| Record Version |
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Official Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
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C571206
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2380-86-1
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524508
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DTXSID20178497
Created by
admin on Mon Mar 31 19:20:12 GMT 2025 , Edited by admin on Mon Mar 31 19:20:12 GMT 2025
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3I03JZ599T
Created by
admin on Mon Mar 31 19:20:12 GMT 2025 , Edited by admin on Mon Mar 31 19:20:12 GMT 2025
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PRIMARY |