Weight | 218.256 g/mol |
---|---|
Formula | C12H14N2O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 3 |
Aromatic Rings | 2 |
Rotatable Bonds | 3 |
4-Methyl-DL-tryptophan (1954-45-6)
4-methyltryptophan, (L)-isomer · 4-methyltryptophan · 4-methyltryptophan, (DL)-isomer
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- The effect of 4-methyltryptophan on growth and enzyme systems of Escherichia coli. (Biochemical Journal, 1956)
- Restoration of Serotonin Biosynthesis in Cell Suspension Cultures of Peganum harmala by Selection for 4-methyltryptophan-tolerant Cell Lines (Journal of Plant Physiology, 1987)
- Use of 4-methylindole or 7-methyl-DL-tryptophan in a transformant selection system based on the feedback-insensitive anthranilate synthase -subunit of tobacco (ASA2) (Plant Cell Reports, 2008)
- Biosynthesis of the actinomycin chromophore. Influence of -, 4-, 5-, and 6-methyl-DL-tryptophan on actinomycin synthesis (Biochimica et Biophysica Acta, 1962)
- The direct oxidative conversion of 2-methyltryptophan to 4-acetylquinoline (Tetrahedron Letters, 1961)
- Inhibition of yeast tRNATrp aminoacylation by 4-methyltryptophan (Archives of Microbiology, 1981)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-methyltryptophan, (L)-isomer
- 4-methyltryptophan
- 4-methyltryptophan, (DL)-isomer
-
SMILESCC1=C2C(=CC=C1)NC=C2CC(C(=O)O)N
-
InChIKeyFPJGLSZLQLNZIW-UHFFFAOYSA-N
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