Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H9NO |
| Molecular Weight | 147.1739 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C2NC=CC2=C1
InChI
InChIKey=DWAQDRSOVMLGRQ-UHFFFAOYSA-N
InChI=1S/C9H9NO/c1-11-8-2-3-9-7(6-8)4-5-10-9/h2-6,10H,1H3
| Molecular Formula | C9H9NO |
| Molecular Weight | 147.1739 |
| 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 |
|---|---|---|
| Mechanism for the direct synthesis of tryptophan from indole and serine: a useful NMR technique for the detection of a reactive intermediate in the reaction mixture. | 2010-10 |
|
| Rotationally resolved electronic spectroscopy of 5-methoxyindole. | 2010-07-14 |
|
| 5-Meth-oxy-1-(3,4,5-trimethoxy-phen-yl)-1H-indole. | 2010-06-16 |
|
| Optimization of the interligand Overhauser effect for fragment linking: application to inhibitor discovery against Mycobacterium tuberculosis pantothenate synthetase. | 2010-04-07 |
|
| The synthesis of 2- and 3-aryl indoles and 1,3,4,5-tetrahydropyrano[4,3-b]indoles and their antibacterial and antifungal activity. | 2009-09-01 |
|
| 4-Des-oxy-4β-[(5-meth-oxy-1H-indol-3-yl)oxalylamino]podophyllotoxin methanol solvate. | 2008-11-13 |
|
| Functional expression and comparative characterization of nine murine cytochromes P450 by fluorescent inhibition screening. | 2008-07 |
|
| The 5-HT3B subunit confers spontaneous channel opening and altered ligand properties of the 5-HT3 receptor. | 2008-03-14 |
|
| Biological targets for isatin and its analogues: Implications for therapy. | 2007-06 |
|
| Nucleophilic reactivities of indoles. | 2006-11-24 |
|
| Simultaneous liquid chromatographic measurement of melatonin and related indoles through post-column electrochemical demethylation and fluorescence derivatization. | 2006-02 |
|
| Indole ring oxidation by activated leukocytes prevents the production of hypochlorous acid. | 2005-11 |
|
| Generation of new protein kinase inhibitors utilizing cytochrome p450 mutant enzymes for indigoid synthesis. | 2004-06-03 |
|
| Daily variation in the concentration of melatonin and 5-methoxytryptophol in the goose pineal gland, retina, and plasma. | 2003-12 |
|
| Daily variation in the concentration of 5-methoxytryptophol and melatonin in the duck pineal gland and plasma. | 2002-05 |
|
| A simple procedure for synthesis of roxindole, a dopamine D2-receptor agonist. | 2001-07 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:36:08 GMT 2025
by
admin
on
Mon Mar 31 19:36:08 GMT 2025
|
| Record UNII |
DQM3AS43PQ
|
| Record Status |
Validated (UNII)
|
| Record Version |
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1006-94-6
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213-745-3
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