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beta-methylcrotonylglycine

structure

Also Known As:

3-methylcrotonylglycine; Glycine, N-(3-methyl-1-oxo-2-butenyl)-

Networked: 8 relevant articles (0 outcomes, 1 trials/studies)

Bio-Agent Context: Research Results

Amino Acids, Peptides, and Proteins: 1
- Amino Acids: 30675
  - Glycine: 5151
    - beta-methylcrotonylglycine: 8

Experts

1.	Anders, Hans Joachim: 1 article (10/2016)
2.	Belmonte, Juan Carlos Izpisua: 1 article (10/2016)
3.	Beyret, Ergin: 1 article (10/2016)
4.	D'Agati, Vivette: 1 article (10/2016)
5.	Darshi, Manjula: 1 article (10/2016)
6.	Ideker, Trey: 1 article (10/2016)
7.	Ju, Wenjun: 1 article (10/2016)
8.	Kretzler, Matthias: 1 article (10/2016)
9.	Miyamoto, Satoshi: 1 article (10/2016)
10.	Mulay, Shrikant R: 1 article (10/2016)

Related Diseases

1.	Acidosis 01/15/1980 - "A child with a history of episodes of metabolic acidosis was found to excrete 3-hydroxyisovaleric acid and 3-methylcrotonylglycine. " 05/01/1993 - "Laboratory studies showed metabolic acidosis, marked lactic acidaemia, hyperammonaemia and increased urinary excretion of 3-hydroxyisovaleric acid, 3-methylcrotonylglycine, 3-hydroxpropionic acid and methylcitric acid. " 11/01/1989 - "Biochemical assays revealed compensated metabolic acidosis, pathologically high lactate and pyruvate concentrations in the blood and cerebro-spinal fluid, as well as increased urinary excretion of 3-OH-isovaleric acid, 3-methylcrotonylglycine and lactate. "
2.	Lactic Acidosis 02/01/2000 - "Laboratory examinations showed hyperglycemia, hyperammonemia, lactic acidosis, and excretion of large amounts of beta-hydroxyisovalerate and beta-methylcrotonylglycine in the urine. " 07/21/1979 - "The third child, who presented with a periorificial candida dermatitis, alopecia, keratoconjunctivitis, and intermittent ataxia at eighteen months of age, had intermittent lactic acidosis and raised excretion of beta-hydroxyproprionate, methylcitrate, beta-methylcrotonylglycine, and beta-hydroxyisovalerate in urine. "
3.	Hyperammonemia 02/01/2000 - "Laboratory examinations showed hyperglycemia, hyperammonemia, lactic acidosis, and excretion of large amounts of beta-hydroxyisovalerate and beta-methylcrotonylglycine in the urine. "
4.	Metabolic Diseases (Metabolic Disease) 03/01/2012 - "Deficiency of 3-methylcrotonyl-CoA carboxylase activity is an inherited metabolic disease biochemically characterized by accumulation and high urinary excretion of 3-methylcrotonylglycine (3MCG), and also of 3-hydroisovalerate in lesser amounts. "
5.	Ketosis 10/01/1981 - "Metabolic characteristics included increased excretion of 3-methylcrotonylglycine, 3-hydroxyisovaleric acid, 3-hydroxypropionic acid, methylcitric acid, and lactic acid, as well as a propensity for the development of ketosis. "

Related Drugs and Biologics

1.	beta-hydroxyisovaleric acid (beta-hydroxy-beta-methylbutyrate)
2.	Acids
3.	2-methylcitric acid
4.	Lactic Acid (Lactate)
5.	Pyruvic Acid (Pyruvate)
6.	Uracil
7.	hydracrylic acid