Search

Displaying results 71 - 80 of 5601 in total
  1. Pathway

    Congenital Bile Acid Synthesis Defect Type III

    smpdb.ca/view/SMP0000318
    Disease

    Congenital Bile Acid Synthesis Defect Type III (CBASIII) is caused by a defect in 25-hydroxycholesterol 7-alpha-hydroxylase, which plays a role in synthesis of bile acids. … The synthesis of primary bile acids from cholesterol occurs via two pathways: the classic neutral pathway involving cholesterol 7-alpha-hydroxylase (CYP7A1), and the acidic pathway involving a distinct

    Drugs: Glycine · NADH · ATP · Iron · Taurine · Mesoheme +9 more
  2. Pathway

    Congenital Bile Acid Synthesis Defect Type II

    smpdb.ca/view/SMP0125689
    Disease

    Chenodeoxycholic acid and cholic acid are decreased in plasma and urine. … Congenital Bile Acid Synthesis Defect Type II is a congenital defect in bile acid synthesis with delta(4)-3-oxosteroid 5-beta-reductase deficiency is caused by mutation in the AKR1D1 gene. 3-oxo-5-beta-steroid

    Drugs: Glycine · NADH · ATP · Iron · Taurine · Mesoheme +9 more
  3. Pathway

    Metabolism and Physiological Effects of Oxalic acid

    smpdb.ca/view/SMP0124875
    Metabolic

    Oxalic acid (oxalate) is a strong dicarboxylic acid that is also a known uremic toxin. It is produced in the body by metabolism of glyoxylic acid or ascorbic acid. … acid using the enzyme aspartate aminotransferase.

    Drugs: Pyridoxal phosphate · Ascorbic acid · Succinic acid · Glutamic acid · Glycine · Proline +4 more
    Enzymes: D-amino-acid oxidase
  4. Pathway

    Metabolsim and Physiological Effects of Argininic acid

    smpdb.ca/view/SMP0125504
    Metabolic

    Glutamic acid is carboxylated into 1-Pyrroline-5-carboxylic acid by the enzyme Delta-1-pyrroline-5-carboxylate synthase. 1-Pyrroline-5-carboxylic acid with glutaric acid synthesize Oxoglutaric acid and … This accumulation causes arginine to instead be converted into α-keto-δ-guanidinovaleric acid by transamination. α-Keto-δ-guanidinovaleric acid is then hydrogenated to form argininic acid.

    Drugs: Pyridoxal phosphate · Arginine · Aspartic acid · Ornithine · L-Glutamine · Adenosine phosphate +10 more
    Enzymes: D-amino-acid oxidase, Neutral amino acid transporter A
  5. Pathway

    Metabolism and Physiological Effects of 4-Hydroxyhippuric Acid

    smpdb.ca/view/SMP0125537
    Metabolic

    4-Hydroxyhippuric, also known as 4-hydroxybenzoylglycine or 4-hydroxyhippate acid, is a metabolite of hippuric acid, and a uremic toxin. … Benzoyl-CoA is then catalyzed by the enzyme glycine N-acyltransferase and a glycine, which produces hippuric acid.

    Drugs: ATP · Calcium · Mesoheme · Benzoic acid · Pyrophosphoric acid
  6. Indication

    Uric Acid Stones

    go.drugbank.com/conditions/DBCOND0078710
    Drugs: Potassium bicarbonate · Potassium sodium hydrogen citrate
    Synonyms: Uric Acid Stones
  7. Indication

    Ascorbic Acid Deficiency

    go.drugbank.com/conditions/DBCOND0118953
    Drugs: Ascorbic acid
    Synonyms: Ascorbic Acid Deficiency, Ascorbic acid defic.
  8. Indication

    Deficiency, Vitamin C

    go.drugbank.com/conditions/DBCOND0154004
    Drugs: Ascorbic acid · Calcium ascorbate
    Synonyms: Ascorbic acid defic., Ascorbic acid deficiency
  9. Drug

    Magnesium

    go.drugbank.com/drugs/DB14513
    ApprovedInvestigational

    Magnesium is classified as an alkaline earth metal and has 2 hydration shells. The element can be found in abundance in the hydrosphere and in mineral salts such as dolomite and magnesium carbonate. Common dietary sources of magnesium in...

    Mixtures: Calcium Folic Acid Plus D ChewableProducts: Kordel’s Magnesium Amino Acid Chelate 750 Capsules
  10. Indication

    Dyspepsia

    go.drugbank.com/conditions/DBCOND0004526
    Drugs: Alginic acid · Almasilate · Aluminium glycinate · Aluminium phosphate · Aluminum hydroxide · Anise oil +27 more
    Synonyms: Acid Dyspepsia, Acid indigestion