Home Other Building Blocks 5-Methoxyindole

5-Methoxyindole

CAS No.:
1006-94-6
Catalog Number:
AG0002GY
Molecular Formula:
C9H9NO
Molecular Weight:
147.1739
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
95%
In Stock USA
United States
$14
- +
25g
95%
In Stock USA
United States
$43
- +
100g
98%(GC)
In Stock USA
United States
$168
- +
500g
98%(GC)
In Stock USA
United States
$465
- +
Product Description
Catalog Number:
AG0002GY
Chemical Name:
5-Methoxyindole
CAS Number:
1006-94-6
Molecular Formula:
C9H9NO
Molecular Weight:
147.1739
MDL Number:
MFCD00005674
IUPAC Name:
5-methoxy-1H-indole
InChI:
InChI=1S/C9H9NO/c1-11-8-2-3-9-7(6-8)4-5-10-9/h2-6,10H,1H3
InChI Key:
DWAQDRSOVMLGRQ-UHFFFAOYSA-N
SMILES:
COc1ccc2c(c1)cc[nH]2
EC Number:
213-745-3
UNII:
DQM3AS43PQ
NSC Number:
521752
Properties
Complexity:
138  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
147.068g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
147.177g/mol
Monoisotopic Mass:
147.068g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
25A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.1  
Literature
Title Journal
Assessment of the pharmacological properties of 5-methoxyindole derivatives at 5-HT4 receptors. The Journal of pharmacy and pharmacology 20120801
Prospective acetylcholinesterase inhibitory activity of indole and its analogs. Bioorganic & medicinal chemistry letters 20120415
Ethyl 3,3,3-trifluoro-2-hy-droxy-2-(5-meth-oxy-1H-indol-3-yl)propionate. Acta crystallographica. Section E, Structure reports online 20110701
1,6-Dihydro-2H-indeno[5,4-b]furan derivatives: design, synthesis, and pharmacological characterization of a novel class of highly potent MT₂-selective agonists. Journal of medicinal chemistry 20110512
2-(1-Ethyl-5-meth-oxy-1H-indol-3-yl)-N-isopropyl-2-oxoacetamide. Acta crystallographica. Section E, Structure reports online 20110501
ATP-binding site of bacterial enzymes as a target for antibacterial drug design. Journal of medicinal chemistry 20110224
N-Cyclo-hexyl-2-(5-meth-oxy-1H-indol-3-yl)-2-oxoacetamide. Acta crystallographica. Section E, Structure reports online 20110201
2-(1-Ethyl-5-meth-oxy-1H-indol-3-yl)-N-(4-meth-oxy-phen-yl)-2-oxoacetamide. Acta crystallographica. Section E, Structure reports online 20110201
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. Magnetic resonance in chemistry : MRC 20101001
Rotationally resolved electronic spectroscopy of 5-methoxyindole. The Journal of chemical physics 20100714
5-Meth-oxy-1-(3,4,5-trimethoxy-phen-yl)-1H-indole. Acta crystallographica. Section E, Structure reports online 20100701
Optimization of the interligand Overhauser effect for fragment linking: application to inhibitor discovery against Mycobacterium tuberculosis pantothenate synthetase. Journal of the American Chemical Society 20100407
The synthesis of 2- and 3-aryl indoles and 1,3,4,5-tetrahydropyrano[4,3-b]indoles and their antibacterial and antifungal activity. Bioorganic & medicinal chemistry letters 20090901
Application of fragment growing and fragment linking to the discovery of inhibitors of Mycobacterium tuberculosis pantothenate synthetase. Angewandte Chemie (International ed. in English) 20090101
4-Des-oxy-4β-[(5-meth-oxy-1H-indol-3-yl)oxalylamino]podophyllotoxin methanol solvate. Acta crystallographica. Section E, Structure reports online 20081201
Functional expression and comparative characterization of nine murine cytochromes P450 by fluorescent inhibition screening. Drug metabolism and disposition: the biological fate of chemicals 20080701
The 5-HT3B subunit confers spontaneous channel opening and altered ligand properties of the 5-HT3 receptor. The Journal of biological chemistry 20080314
Biological targets for isatin and its analogues: Implications for therapy. Biologics : targets & therapy 20070601
Nucleophilic reactivities of indoles. The Journal of organic chemistry 20061124
Simultaneous liquid chromatographic measurement of melatonin and related indoles through post-column electrochemical demethylation and fluorescence derivatization. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20060201
Indole ring oxidation by activated leukocytes prevents the production of hypochlorous acid. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 20051101
Generation of new protein kinase inhibitors utilizing cytochrome p450 mutant enzymes for indigoid synthesis. Journal of medicinal chemistry 20040603
Daily variation in the concentration of melatonin and 5-methoxytryptophol in the goose pineal gland, retina, and plasma. General and comparative endocrinology 20031201
Daily variation in the concentration of 5-methoxytryptophol and melatonin in the duck pineal gland and plasma. Journal of pineal research 20020501
A simple procedure for synthesis of roxindole, a dopamine D2-receptor agonist. Archiv der Pharmazie 20010701
Development of a pharmacophore for inhibition of human liver cytochrome P-450 2D6: molecular modeling and inhibition studies. Journal of medicinal chemistry 19930430
Properties