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Ethylmalonic encephalopathy (EE) is a rare
autosomal recessive inborn error of metabolism.
Patients affected with EE are
typically identified shortly after...
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Organic acidemia is a term used to
classify a
group of
metabolic disorders which disrupt normal amino acid metabolism,
particularly branched-chain amino...
- that of amobarbital, the only
difference being that the
alkylation of α-
ethylmalonic ester is
carried out with 2-bromopentane in
place of 1-bromo-3-methylbutane...
- enanthate, an
estrogen which is used in
combined injectable birth control Ethylmalonic encephalopathy, a
genetic disorder Ethinylestradiol, an
estrogen which...
-
thrombocytosis Essential thrombocytosis Esthesioneuroblastoma Ethylmalonic aciduria Ethylmalonic adipic aciduria Euhidrotic ectodermal dysplasia Eumycetoma...
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Glutaric acidemia type 2 is an
autosomal recessive metabolic disorder that is
characterised by
defects in the
ability of the body to use
proteins and fats...
-
ester synthesis using ethyl bromide leads to the
formation of α-phenyl-α-
ethylmalonic ester. Finally, a
condensation reaction with urea
gives phenobarbital...
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Protein ETHE1, mitochondrial, also
known as "
ethylmalonic encephalopathy 1 protein" and "per
sulfide dioxygenase", is a
protein that in
humans is encoded...
-
series of
substrates of the
upstream flavoenzyes, e.g. glutaric, lactic,
ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and
isovaleric acids. ETF is...
- 111-30-8 C5H8O2
angelic acid 565-63-9 C5H8O2
tiglic acid 80-59-1 C5H8O4
ethylmalonic acid 601-75-2 C5H8O4
methylene diacetate 628-51-3 C5H8O4
glutaric acid...
