enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Tetrahydrobiopterin - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrobiopterin

    Tetrahydrobiopterin (BH 4, THB), also known as sapropterin (), [5] [6] is a cofactor of the three aromatic amino acid hydroxylase enzymes, [7] used in the degradation of amino acid phenylalanine and in the biosynthesis of the neurotransmitters serotonin (5-hydroxytryptamine, 5-HT), melatonin, dopamine, norepinephrine (noradrenaline), epinephrine (adrenaline), and is a cofactor for the ...

  3. Benazepril - Wikipedia

    en.wikipedia.org/wiki/Benazepril

    Benazepril, sold under the brand name Lotensin among others, is a medication used to treat high blood pressure, heart failure, and diabetic kidney disease. [2] It is a reasonable initial treatment for high blood pressure. [2]

  4. Phenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylboronic_acid

    The orthorhombic crystals use hydrogen bonding to form units made up of two molecules. [3] These dimeric units are combined to give an extended hydrogen-bonded network . The molecule is planar with a minor bend around the C-B bond of 6.6° and 21.4° for the two PhB(OH) 2 molecules.

  5. Tenapanor - Wikipedia

    en.wikipedia.org/wiki/Tenapanor

    Tenapanor, sold under the brand name Ibsrela among others, is a medication used for the treatment of adults with a disease of the gut called irritable bowel syndrome with constipation commonly referred to as IBS-C. [3] [5] It is used in form of tenapanor hydrochloride. [3]

  6. PRL-8-53 - Wikipedia

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

    PRL-8-53 is relatively non-toxic, with an oral LD 50 in mice of 860 mg/kg, giving the drug a high therapeutic index. Doses above 8 mg/kg have brief hypotensive effects in canines. High doses depress motor activity in the rat and mouse, with the ED 50 for a 50% reduction in motor activity of mice at 160 mg/kg. PRL-8-53 displays spasmolytic ...

  7. Gemigliptin - Wikipedia

    en.wikipedia.org/wiki/Gemigliptin

    Gemigliptin was rapidly absorbed after single oral dosing and the compound was eliminated with a half-life of 3.6 h, 5.2 h, and 5.4 h in the rat, dog, and monkey, respectively. [medical citation needed] The bioavailability of gemigliptin in the rat, dog, and monkey was species-dependent with the values of 94%, 73%, and 26%, respectively ...

  8. Chlorpromazine - Wikipedia

    en.wikipedia.org/wiki/Chlorpromazine

    RR 4.9 CI 2.3 to 10.4: Very low (estimate of effect uncertain) Sedation: 3 times more likely to cause sedation, around 30% with chlorpromazine: RR 2.8 CI 2.3 to 3.5 Acute movement disorder: 3.5 times more likely to cause easily reversible but unpleasant severe stiffening of muscles, around 6% with chlorpromazine: RR 3.5 CI 1.5 to 8.0 Parkinsonism

  9. Daridorexant - Wikipedia

    en.wikipedia.org/wiki/Daridorexant

    At doses of 25 to 50 mg and in terms of treatment–placebo difference, it reduces LPS by 6 to 12 minutes, reduces WASO by 10 to 23 minutes, and increases subjective TST by 10 to 22 minutes. [ 1 ] [ 18 ] Daridorexant has also been found to improve daytime functioning at a dose of 50 mg but not at 25 mg. [ 17 ]