Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H9NO |
| Molecular Weight | 123.1525 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(O)=C(N)C=C1
InChI
InChIKey=HCPJEHJGFKWRFM-UHFFFAOYSA-N
InChI=1S/C7H9NO/c1-5-2-3-6(8)7(9)4-5/h2-4,9H,8H2,1H3
| Molecular Formula | C7H9NO |
| Molecular Weight | 123.1525 |
| 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 |
|---|---|---|
| Vibrational spectroscopy investigation using ab initio and density functional theory analysis on the structure of 2-amino-5-methylphenol. | 2007-06 |
|
| Effect of natural phenol derivatives on skeletal type sarcoplasmic reticulum Ca2+ -ATPase and ryanodine receptor. | 2007 |
|
| A novel kinetic determination of dissolved chromium species in natural and industrial waste water. | 2006-09-15 |
|
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005-06 |
|
| Final report on the safety assessment of 6-Amino-m-Cresol, 6-Amino-o-Cresol, 4-Amino-m-Cresol, 5-Amino-4-Chloro-o-Cresol, 5-Amino-6-Chloro-o-Cresol, and 4-Chloro-2-Aminophenol. | 2004 |
|
| A novel phenoxazine derivative suppresses proliferation of human endometrial adenocarcinoma cell lines, inducing G2M accumulation and apoptosis. | 2003-07-29 |
|
| Antiviral activity of 2-amino-4,4alpha-dihydro-4alpha-7-dimethyl-3H-phenoxazine-3-one on poliovirus. | 2003-07 |
|
| A novel meta-cleavage dioxygenase that cleaves a carboxyl-group-substituted 2-aminophenol. Purification and characterization of 4-amino-3-hydroxybenzoate 2,3-dioxygenase from Bordetella sp. strain 10d. | 2002-12 |
|
| Antitumor activity of a phenoxazine compound, 2-amino-4,4alpha-dihydro-4alpha,7-dimethyl-3H-phenoxazine-3-one against human B cell and T cell lymphoblastoid cell lines: induction of mixed types of cell death, apoptosis, and necrosis. | 2002-07 |
|
| An improved method for the rapid preparation of 2-amino-4,4a-dihydro-4a,7-dimethyl-3H-phenoxazine-3-one, a novel antitumor agent. | 2001-04-23 |
|
| Prevention of growth of human lung carcinoma cells and induction of apoptosis by a novel phenoxazinone, 2-amino-4,4alpha-dihydro-4alpha,7-dimethyl-3H-phenoxazine-3-one. | 2001-04 |
|
| Antitumor effects of a novel phenoxazine derivative on human leukemia cell lines in vitro and in vivo. | 2001-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:21:33 GMT 2025
by
admin
on
Mon Mar 31 19:21:33 GMT 2025
|
| Record UNII |
QCG4ES2A26
|
| Record Status |
Validated (UNII)
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| Record Version |
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220-620-7
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2835-98-5
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C077618
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DTXSID20182594
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QCG4ES2A26
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322874
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76082
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