• Thioamides function as antithyroid agents mainly by inhibiting iodide organification and coupling processes, thereby preventing synthesis of thyroid hormones. (medscape.com)
  • Liver function test results should be obtained to monitor for liver toxicity caused by thioamides (antithyroid medications). (medscape.com)
  • Thioamides are typically prepared by treating amides with phosphorus sulfides such as phosphorus pentasulfide, a reaction first described in the 1870s. (wikipedia.org)
  • Thioamides inhibit the enzyme thyroid peroxidase in the thyroid, reducing the synthesis of triiodothyronine (T3) and thyroxine (T4), thereby blocking uptake of iodotyrosines from the colloid. (wikipedia.org)
  • An operationally simple and metal-free approach is described for the synthesis of pyrazole-tethered thioamide and amide conjugates. (nih.gov)
  • Colorless, odorless crystals that are used extensively in research laboratories for the preparation of polyacrylamide gels for electrophoresis and in organic synthesis, and polymerization. (nih.gov)
  • The most widely applied strategies for their synthesis rely on cross-coupling reactions but the preparation of structurally diverse and nonsymmetrical tetraarylmethanes remains challenging. (thieme.de)
  • Fifth chapter includes the preparation of few important bio-active compounds. (journaltocs.ac.uk)
  • A thioamide (rarely, thionamide, but also known as thiourylenes) is a functional group with the general structure R1−C(=S)−NR2R3, where R1, R2 and R3 are any groups (typically organyl groups or hydrogen). (wikipedia.org)
  • Thioamides may rarely cause severe hematologic side effects, but routine screening for these rare events is not cost-effective. (medscape.com)
  • The thioamides were generated by employing a three-component reaction of diverse pyrazole C-3/4/5 carbaldehydes, secondary amines, and elemental sulfur in a single synthetic operation. (nih.gov)
  • One of the best-known thioamides is thioacetamide, which is used as a source of the sulfide ion and is a building block in heterocyclic chemistry. (wikipedia.org)
  • Only oral preparations are available, but they have been used as retention enemas in patients in whom oral intake is not possible or is contraindicated. (medscape.com)
  • The present invention relates to new 1-aralkylpyrazoles, a process for their preparation and their use as agents for combating pests. (justia.com)