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  2. Calcium channel blocker - Wikipedia

    en.wikipedia.org/wiki/Calcium_channel_blocker

    Calcium channel blockers (CCB), calcium channel antagonists or calcium antagonists [2] are a group of medications that disrupt the movement of calcium (Ca 2+ ) through calcium channels . [ 3 ] Calcium channel blockers are used as antihypertensive drugs , i.e., as medications to decrease blood pressure in patients with hypertension .

  3. List of biomolecules - Wikipedia

    en.wikipedia.org/wiki/List_of_biomolecules

    This is a list of articles that describe particular biomolecules or types of biomolecules. ... List of organic compounds; List of proteins ... a non-profit organization.

  4. 1,4-Dihydropyridine - Wikipedia

    en.wikipedia.org/wiki/1,4-Dihydropyridine

    The parent compound is uncommon, [2] but derivatives of 1,4-dihydropyridine are important commercially and biologically. The pervasive cofactors NADH and NADPH are derivatives of 1,4-dihydropyridine. 1,4-Dihydropyridine-based drugs are L-type calcium channel blockers, used in the treatment of hypertension. 1,2-Dihydropyridines are also known ...

  5. Lists of molecules - Wikipedia

    en.wikipedia.org/wiki/Lists_of_molecules

    This is an index of lists of molecules (i.e. by year, number of atoms, etc.). Millions of molecules have existed in the universe since before the formation of Earth. Three of them, carbon dioxide, water and oxygen were necessary for the growth of life.

  6. ATC code C08 - Wikipedia

    en.wikipedia.org/wiki/ATC_code_C08

    ATC code C08 Calcium channel blockers is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes developed by the World Health Organization (WHO) for the classification of drugs and other medical products. [1] [2] [3] Subgroup C08 is part of the anatomical group C Cardiovascular system ...

  7. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Hantzsch dihydropyridine synthesis, Hantzsch pyridine synthesis Hantzsch pyridine synthesis , Gattermann–Skita synthesis , Guareschi–Thorpe condensation , Knoevenagel–Fries modification Hantzsch–Collidin synthesis

  8. Hantzsch pyridine synthesis - Wikipedia

    en.wikipedia.org/wiki/Hantzsch_pyridine_synthesis

    [1] [2] The initial reaction product is a dihydropyridine which can be oxidized in a subsequent step to a pyridine. [3] The driving force for this second reaction step is aromatization. This reaction was reported in 1881 by Arthur Rudolf Hantzsch. A 1,4-dihydropyridine dicarboxylate is also called a 1,4-DHP compound or a Hantzsch ester.

  9. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).