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  2. Pentamine - Wikipedia

    en.wikipedia.org/wiki/Pentamine

    This drug article relating to the nervous system is a stub. You can help Wikipedia by expanding it.

  3. Pentamidine - Wikipedia

    en.wikipedia.org/wiki/Pentamidine

    Common side effects of the inhaled form include wheezing, cough, and nausea. [1] It is unclear if doses should be changed in those with kidney or liver problems. [1] Pentamidine is not recommended in early pregnancy but may be used in later pregnancy. [1] Its safety during breastfeeding is unclear. [3]

  4. 1,3-Benzodioxolyl-N-ethylpentanamine - Wikipedia

    en.wikipedia.org/wiki/1,3-Benzodioxolyl-N-ethyl...

    It is the N-ethyl analog of 1,3-benzodioxolylpentanamine (BDP; K). Ethyl-K was first synthesized by Alexander Shulgin. In his book PiHKAL ("Phenethylamines i Have Known And Loved"), the minimum dosage is listed as 40 mg and the duration is unknown. [1] [2] Very little is known about the pharmacology, pharmacokinetics, effects, and toxicity of ...

  5. Eutylone - Wikipedia

    en.wikipedia.org/wiki/Eutylone

    Eutylone (also known as β-keto-1,3-benzodioxolyl-N-ethylbutanamine, bk-EBDB, and N-ethylbutylone) is a stimulant and empathogenic drug of the phenethylamine, amphetamine, phenylisobutylamine, and cathinone families which was developed in the 1960s, [3] [4] which is classified as a designer drug. [5]

  6. Triethylenetetramine - Wikipedia

    en.wikipedia.org/wiki/Triethylenetetramine

    Triethylenetetramine (TETA and trien), also known as trientine when used medically, is an organic compound with the formula [CH 2 NHCH 2 CH 2 NH 2] 2. The pure free base is a colorless oily liquid, but, like many amines, older samples assume a yellowish color due to impurities resulting from air oxidation. It is soluble in polar solvents.

  7. Methenamine - Wikipedia

    en.wikipedia.org/wiki/Methenamine

    Methenamine, also known as 1,3,5,7-tetraazaadamantane, is a simple cyclic hydrocarbon with a cage-like structure and is similar in structure to adamantane (tricyclo[3.3.1.1 3,7]decane). [ 2 ] [ 13 ] [ 7 ] [ 8 ] [ 37 ] It is specifically the analogue of adamantane in which the carbon atoms at the 1, 3, 4, and 7 positions have been replaced with ...

  8. Emetine - Wikipedia

    en.wikipedia.org/wiki/Emetine

    It does this by binding to the 40S subunit of the ribosome. [3] This can thus be used in the study of protein degradation in cells. Mutants resistant to emetine are altered in the 40S ribosomal subunit (S14 protein), [ 4 ] [ 5 ] and they exhibit cross-resistance to cryptopleurine, tylocrebrine, cephaeline and tubulosine, but not other ...

  9. Corvalol - Wikipedia

    en.wikipedia.org/wiki/Corvalol

    Ethyl ester of α-bromoisovaleric acid. According to the Farmak product label of Corvalol oral solution, the composition per 1 mL (26 drops) is as follows: [6] Ethyl ester of α-bromoisovaleric acid (ethyl 2-bromo-3-methylbutyrate) — 20 mg; Phenobarbital — 18.26 mg; Peppermint oil — 1.42 mg; Inactive ingredients: stabilizer, ethanol 96% ...