4-hydroxycyclohexylacetic acid

同

4-HCAA

WordNet

1. street name for lysergic acid diethylamide (同)back breaker, battery-acid, dose, dot, Elvis, loony toons, Lucy in the sky with diamonds, pane, superman, window pane, Zen
2. any of various water-soluble compounds having a sour taste and capable of turning litmus red and reacting with a base to form a salt
3. having the characteristics of an acid; "an acid reaction"

PrepTutorEJDIC

1. 酸性の / 酸味のある,すっぱい(sour) / (言葉・態度などが)厳しい,しんらつな / 酸 / すっぱいもの / 《俗》=LSD

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• 1. セカンドラインの抗結核療法 second line antituberculous therapy
• 2. 薬剤耐性結核の診断、治療、および予防 diagnosis treatment and prevention of drug resistant tuberculosis
• 3. 肝疾患の有無と血漿中のアスパラギン酸アミノトランスフェラーゼおよびアラニン・
  アミノトランスフェラーゼ濃度のパターン patterns of plasma aspartate and alanine aminotransferase levels with and without liver disease
• 4. 骨格系結核 skeletal tuberculosis
• 5. 妊娠中の結核 tuberculosis in pregnancy

English Journal

• Long-term follow up of a new case of hawkinsinuria.

• Lehnert W1, Stögmann W, Engelke U, Wevers RA, van den Berg GB.
• European journal of pediatrics.Eur J Pediatr.1999 Jul;158(7):578-82.
• Hawkinsinuria is a rarely diagnosed autosomal dominantly transmitted inborn error of tyrosine metabolism with impaired conversion of 4-hydroxyphenylpyruvate to homogentisate. As a consequence of the defective 4-hydroxyphenylpyruvate dioxigenase activity, large amounts of the unusual, ninhydrin-posit
• PMID 10412819

• Hawkinsinuria in two families.

• Borden M1, Holm J, Leslie J, Sweetman L, Nyhan WL, Fleisher L, Nadler H, Lewis D, Scott CR.
• American journal of medical genetics.Am J Med Genet.1992 Sep 1;44(1):52-6.
• Hawkinsinuria, a disorder of tyrosine metabolism has been documented in two families in the United States, in one of which there was clear evidence of autosomal dominant inheritance. Metabolic acidosis and failure to thrive appear to be confined to infancy. Tyrosyl metabolites and 5-oxoproline are a
• PMID 1519651

• Hawkinsinuria--identification of quinolacetic acid and pyroglutamic acid during an acidotic phase.

• Hocart CH, Halpern B, Hick LA, Wong CO.
• Journal of chromatography.J Chromatogr.1983 Jul 8;275(2):237-43.
• A second Australian family with the genetic disease Hawkinsinuria has been identified. Affected members excrete hawkinsin and cis- and trans-4-hydroxycyclohexylacetic acid. An infant in this family presented with metabolic acidosis and excreted quinolacetic acid and pyroglutamic acid in the urine to
• PMID 6619234

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「4-HCAA」

「4-HCAA」

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4-hydroxycyclohexylacetic acid