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  2. List of chemical compounds in coffee - Wikipedia

    en.wikipedia.org/wiki/List_of_chemical_compounds...

    Interactions between chemical compounds also is a frequent area of taxonomy, as are the major organic chemistry categories (protein, carbohydrate, lipid, etc.) that are relevant to the field. In the field of aroma and flavor alone, Flament gives a list of 300 contributing chemicals in green beans, and over 850 after roasting.

  3. Caffeine - Wikipedia

    en.wikipedia.org/wiki/Caffeine

    One biosynthetic route of caffeine, as performed by Camellia and Coffea species [202] [203] One laboratory synthesis of caffeine [204] [205] The biosynthesis of caffeine is an example of convergent evolution among different species. [206] [207] [208] Caffeine may be synthesized in the lab starting with 1,3-dimethylurea and malonic acid.

  4. DMPX - Wikipedia

    en.wikipedia.org/wiki/DMPX

    DMPX (3,7-dimethyl-1-propargylxanthine) is a caffeine analog which displays affinity for A 2 adenosine receptors, in contrast to the A 1 subtype receptors. [1] DMPX had 28 times and 15 times higher potency than caffeine in blocking, respectively, the peripheral and central effects of the adenosine agonist NECA.

  5. Glucuronolactone - Wikipedia

    en.wikipedia.org/wiki/Glucuronolactone

    Glucuronolactone is an ingredient used in some energy drinks, [2] often in unnaturally high doses. Research into Glucuronolactone is too limited to assert claims about its safety [8] The European Food Safety Authority (EFSA) has concluded that it is unlikely that glucurono-γ-lactone would have any interaction with caffeine, taurine, alcohol or the effects of exercise.

  6. Step function - Wikipedia

    en.wikipedia.org/wiki/Step_function

    The product of a step function with a number is also a step function. As such, the step functions form an algebra over the real numbers. A step function takes only a finite number of values. If the intervals , for =,, …, in the above definition of the step function are disjoint and their union is the real line, then () = for all .

  7. Adenosine receptor - Wikipedia

    en.wikipedia.org/wiki/Adenosine_receptor

    Caffeine keeps you awake by blocking adenosine receptors. Each type of adenosine receptor has different functions, although with some overlap. [3] For instance, both A 1 receptors and A 2A play roles in the heart, regulating myocardial oxygen consumption and coronary blood flow, while the A 2A receptor also has broader anti-inflammatory effects throughout the body. [4]

  8. Caffeine dependence - Wikipedia

    en.wikipedia.org/wiki/Caffeine_dependence

    Caffeine dependence can cause a host of physiological effects if caffeine consumption is not maintained. Withdrawal symptoms may include headaches, fatigue, difficulty concentrating, lack of motivation, mood swings, nausea, insomnia, dizziness, cardiac issues, hypertension, anxiety, backaches, and joint pain; these can range in severity from mild to severe. [18]

  9. Additive effect - Wikipedia

    en.wikipedia.org/wiki/Additive_effect

    Additive effect often occurs when two similar drugs are taken together to achieve the same degree of therapeutic effect while reducing the specific adverse effect of one particular drug. For example, aspirin, paracetamol, and caffeine are formulated together to treat pain caused by tension headaches and migraine .