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Methylthiouracil

Chemical compound

Methylthiouracil

Chemical compound

FieldValue
verifiedrevid437194533
IUPAC_name6-methyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
imageMethylthiouracil.svg
image_classskin-invert-image
width180
image2Methylthiouracil-3D-balls.png
image_class2bg-transparent
Drugs.com
pregnancy_AU
pregnancy_US
legal_AU
legal_CA
legal_UK
legal_US
CAS_number56-04-2
ATC_prefixH03
ATC_suffixBA01
PubChem667493
ChEMBL1330588
UNII_Ref
UNIIQW24888U5F
KEGG_Ref
KEGGC19265
ChemSpiderID580871
C5H=6N=2O=1S=1
smilesCC1=CC(=O)NC(=S)N1
StdInChI1S/C5H6N2OS/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9)
StdInChIKeyHWGBHCRJGXAGEU-UHFFFAOYSA-N

|Drugs.com = Methylthiouracil is an organosulfur compound that is used antithyroid preparation. It is a thioamide, closely related to propylthiouracil. Methylthiouracil is not used clinically in the United States, it has a similar mechanism of action and side effect to that of propylthiouricil. The drug acts to decrease the formation of stored thyroid hormone, as thyroglobulin in the thyroid gland. The clinical effects of the drug to treat the hyperthyroid state can have a lag period of up to two weeks, depending on the stores of thyroglobulin and other factors.

Synthesis

url = https://zenodo.org/record/1934608}}</ref>

Methylthiouracil is prepared quite simply by condensation of ethyl acetoacetate with thiourea.

Further work in this series shows that better activity was obtained by incorporation of a lipophilic side chain.

References

References

  1. (1886). "I. Zur Condensation von Thioharnstoff und Acetessigäther.". Justus Liebigs Annalen der Chemie.
  2. (April 2004). "Synthesis of nucleosides". Organic Reactions.
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