| Weight | 205.213 g/mol |
|---|---|
| Formula | C11H11NO3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
5-Methoxyindole-3-acetic acid (608-07-1, 3471-31-6)
5-methoxyindoleacetic acid
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- Isolation of melatonin and 5-methoxyindole-3-acetic acid from bovine pineal glands. (Journal of Biological Chemistry, 1960)
- ISOLATION OF 5-METHOXYINDOLE-3-ACETIC ACID FROM BOVINE PINEAL GLANDS1 (Journal of the American Chemical Society, 1959)
- Analysis of melatonin, 5-methoxytryptophol and 5-methoxyindoleacetic acid in the pineal gland and retina of hamster by capillary column gas chromatographymass spectrometry (Journal of Chromatography B: Biomedical Sciences and Applications, 1984)
- The pineal gland of the mole (Talpa europaea L.) VII. Activity of hydroxyindole-O-methyltransferase (HIOMT) in the formation of 5-methoxytryptophan, 5-methoxytryptamine, 5-methoxyindole-3-acetic acid, 5-methoxytryptophol and melatonin in the eyes and the pineal gland (Journal of Neural Transmission, 1981)
- Secretion of the Methoxyindoles Melatonin, 5-Methoxytryptophol, 5-Methoxyindoleacetic Acid, and 5-Methoxytryptamine from Trout Pineal Organs in Superfusion Culture: Effects of Light Intensity (General and Comparative Endocrinology, 1996)
- Demonstration of antifungal and anti-human immunodeficiency virus reverse transcriptase activities of 6-methoxy-2-benzoxazolinone and antibacterial activity of the pineal indole 5-methoxyindole-3-acetic acid (Comparative Biochemistry and Physiology C-toxicology & Pharmacology, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-methoxyindoleacetic acid
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SMILESCOC1=CC2=C(C=C1)NC=C2CC(=O)O
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InChIKeyCOCNDHOPIHDTHK-UHFFFAOYSA-N
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