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  2. Phenylglycine - Wikipedia

    en.wikipedia.org/wiki/Phenylglycine

    Phenylglycine is the organic compound with the formula C 6 H 5 CH(NH 2)CO 2 H. It is a non-proteinogenic alpha amino acid related to alanine, but with a phenyl group in place of the methyl group. It is a white solid. The compound exhibits some biological activity. [1]

  3. Glycine methyl ester hydrochloride - Wikipedia

    en.wikipedia.org/wiki/Glycine_methyl_ester...

    [2] [3] Upon treatment with base, the salt converts to glycine methyl ester. [4] Glycine methyl ester (and other esters of glycine) are not shelf-stable, tending to polymerize when stored at room temperature [4] or convert to diketopiperazine. The hydrochloride is shelf-stable.

  4. PRL-8-53 - Wikipedia

    en.wikipedia.org/wiki/PRL-8-53

    PRL-8-53 is a nootropic substituted phenethylamine that has been shown to act as a hypermnesic drug in humans; it was first synthesized by medical chemistry professor Nikolaus Hansl at Creighton University in the 1970s as part of his work on amino ethyl meta benzoic acid esters. [1] [2]

  5. Glycine - Wikipedia

    en.wikipedia.org/wiki/Glycine

    2 H 3 N + CH 2 COO − → H 3 N + CH 2 CONHCH 2 COO − + H 2 O. Pyrolysis of glycine or glycylglycine gives 2,5-diketopiperazine, the cyclic diamide. [35] Glycine forms esters with alcohols. They are often isolated as their hydrochloride, such as glycine methyl ester hydrochloride. Otherwise, the free ester tends to convert to diketopiperazine.

  6. Category:Methyl esters - Wikipedia

    en.wikipedia.org/wiki/Category:Methyl_esters

    Methyl esters are esters of methanol. Subcategories. This category has only the following subcategory. ... Methyl 2-fluoroacrylate; Methyl 4-iodobenzoate; Methyl acetate;

  7. N-Phenylacetyl-L-prolylglycine ethyl ester - Wikipedia

    en.wikipedia.org/wiki/N-Phenylacetyl-L...

    N-Phenylacetyl-l-prolylglycine ethyl ester is promoted as a nootropic and is a prodrug of cyclic glycine-proline. [a] [2] Other names include the brand name Noopept (Russian: Ноопепт), developmental code GVS-111, and proposed INN omberacetam. [2] [3] [4] Its synthesis was first reported in 1996. [2] It is orally available.

  8. Methyl phenylacetate - Wikipedia

    en.wikipedia.org/wiki/Methyl_phenylacetate

    Methyl phenylacetate is an organic compound that is the methyl ester of phenylacetic acid, with the structural formula C 6 H 5 CH 2 CO 2 CH 3. It is a colorless liquid that is only slightly soluble in water, but soluble in most organic solvents. Methyl phenylacetate has a strong odor similar to honey.

  9. Pharmacokinetics of testosterone - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics_of...

    [2] [27] Substitution dosages of oral testosterone in men are in the range of 400 to 800 mg/day. [27] [28] Such doses exceed the amount of testosterone produced by the body, which is approximately 7 mg/day, by approximately 100-fold. [2] [27] [28] The elimination half-life of oral testosterone is rapid at about 5 to 7 hours.