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3-methylcholanthrene a highly carcinogenic polycyclic aromatic hydrocarbon synthesized by pyrolytic degradation of cholic acid, deoxycholic acid, or cholesterol. It is a procarcinogen that requires metabolic activation to exert a mutagenic effect and is widely used in laboratory studies of chemical carcinogenesis. Abbreviated MCA.
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3-methylcrotonic acid crotonic acid methylated at the 3 carbon; it is excreted at elevated levels in urine when 3-methylcrotonoyl-CoA carboxylase activity is impaired.
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3-methylcrotonyl the radical of 3-methylcrotonic acid; the thioester formed with coenzyme A, 3-methylcrotonyl CoA, is an intermediate in the degradation of leucine.
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3-methylcrotonyl CoA carboxylase deficiency an autosomal recessive aminoacidopathy due to deficiency of methylcrotonoyl-CoA carboxylase, characterized by increased urine levels of 3-methylcrotonylglycine, 3-methylcrotonic acid, and 3-hydroxyisovaleric acid and variable presentation of mental retardation, central nervous system dysfunction, and muscular atrophy. Written also β-methylcrotonyl CoA carboxylase deficiency.
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3-methylcrotonylglycine a conjugate of 3-methylcrotonic acid and glycine, formed and excreted in excess in the urine when 3-methylcrotonoyl-CoA carboxylase activity is impaired.
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