Indole

From Health Encyclopedia

Contents 1 Used for 2 See for 3 Broader Terms 4 Narrower Terms 5 Facts (generated by robot; please edit if you find it inaccurate)

Used for

crinan alkaloid, crinine, haemanthidine, hydroxyindole, oxindole

See for

bufotenine

Broader Terms

pyrrole

Narrower Terms

indoleacetate, indoleamine, methoxyindole, phthalocyanin, pyridoindole, sumatriptan, tryptamine

Facts (generated by robot; please edit if you find it inaccurate)

• The indole is then intramolecularly channeled to the b-subunit for further synthesis.
• Johnson Space Center Toxicology Group Biomedical Operations and Research Branch Houston, Texas Physical and Chemical Properties 1f55 Indole is a colorless crystalline solid.
• Additionally, indole is further catabolized in the DIBOA/DIMBOA pathway by a series of cytochrome P450-dependent monooxygenases to form DIBOA which is further converted to DIMBOA in a two-step hydroxylation/methylation at position C7 [ Frey03 ] .
• In a single turnover experiment monitoring the conversion of radiolabeled IGP to tryptophan, only a trace of indole is detectable (less than or equal to 1% of the IGP), implying that the reaction of indole to form tryptophan must be quite fast (greater than or equal to 1000 s-1).
• SIM tubes (Sulfide, Indole, Motility) Indole is a by-product of the metabolic breakdown of the amino acid tryptophan used by some microbes.

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