Tryptoline Explained

Tryptoline, also known as tetrahydro-β-carboline and tetrahydronorharmane, is a natural organic derivative of beta-carboline. It is an alkaloid chemically related to tryptamines. Derivatives of tryptoline have a variety of pharmacological properties and are known collectively as tryptolines.[1]

Pharmacology

Tryptolines are competitive selective inhibitors of the enzyme monoamine oxidase type A (MAO-A). 5-Hydroxytryptoline and 5-methoxytryptoline (pinoline) are the most active monoamine oxidase inhibitors (MAOIs) with IC50s of 0.5 μM and 1.5 μM respectively.[2]

Tryptolines are also potent reuptake inhibitors of serotonin and epinephrine, with a significantly greater selectivity for serotonin.

In vivo formation of tryptolines has been a matter of controversy.

See also

Notes and References

  1. Web site: Tryptoline . pubchem.ncbi.nlm.nih.gov.
  2. Youdim . N.B.H. . Oppenheim . B. . The effect of tryptolines (1, 2, 3, 4-tetrahydro-β-carbolines) on monoamine metabolism and the platelet aggregation response in human platelets . Neuroscience . April 1981 . 6 . 4 . 801–810 . 10.1016/0306-4522(81)90163-9 . 7242917 . 37681465 .