uracil's Usage Examples:

uracil mustard between 1958 and 1970 were reviewed.

By using urea, guanidine, thiourea and related compounds instead of amidines, one obtains the uracils.

Hydrouracil, C4H602N2, is obtained by the action of bromine and caustic alkalis on succinamide (H.

Theoretical relative energies and free energies for isolated uracil and thymine tautomers support the existence of the canonical form only.

4-Methyluracil, C5H602N2, has long been known, having first been synthesized by R.

Nucleic acid is at present of unknown constitution; decomposition products are: phosphoric acid, uracil or 2.

Uracil and its homologues may be obtained in many cases from the hydrouracils by the action of bromine, and subsequent elimination of the elements of hydrobromic acid; or by the condensation of aceto-acetic ester and related substances with urea, thiourea, guanidine, 'c.

The oxyderivatives of the tetrahydroand hexahydro-pyrimidines are the uracils and the ureides of malonic acid (see PuRIN).

pyrimidine analog 5-fluorouracil used principally in colon and breast cancer.

METHODS: Records of patients treated with uracil mustard between 1958 and 1970 were reviewed.

Synonyms:

U, nucleotide, ribonucleic acid, RNA, base,

Antonyms:

outfield, noble, incidental, genuine, legitimate,