2-Oxo-3-phenylpropanoate (BioDeep_00000897540)
代谢物信息卡片
2-Oxo-3-phenylpropanoate
化学式: C9H7O3- (163.0395172)
中文名称:
谱图信息:
最多检出来源 Homo sapiens(blood) 33.33%
分子结构信息
SMILES: C1=CC=C(C=C1)CC(=O)C(=O)[O-]
InChI: InChI=1S/C9H8O3/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5H,6H2,(H,11,12)/p-1
描述信息
COVID info from COVID-19 Disease Map
Corona-virus
Coronavirus
SARS-CoV-2
COVID-19
SARS-CoV
COVID19
SARS2
SARS
同义名列表
1 个代谢物同义名
相关代谢途径
Reactome(6)
BioCyc(7)
- superpathway of L-phenylalanine biosynthesis
- superpathway of aromatic amino acid biosynthesis
- superpathway of chorismate metabolism
- L-phenylalanine degradation IV (mammalian, via side chain)
- L-phenylalanine biosynthesis I
- phenylalanine degradation IV (mammalian, via side chain)
- terrequinone A biosynthesis
PlantCyc(2)
代谢反应
72 个相关的代谢反应过程信息。
Reactome(56)
- Phenylalanine and tyrosine catabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine and tyrosine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine and tyrosine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine and tyrosine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine and tyrosine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA - Phenylalanine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine and tyrosine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine and tyrosine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism:
L-Trp + Oxygen ⟶ NFK - Phenylalanine and tyrosine catabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism:
L-Trp + Oxygen ⟶ NFK - Phenylalanine and tyrosine metabolism:
4aOH-BH4 ⟶ H2O + qDHB - Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism:
L-Trp + Oxygen ⟶ NFK - Phenylalanine and tyrosine catabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism:
L-Trp + Oxygen ⟶ NFK - Phenylalanine and tyrosine catabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism:
L-Trp + Oxygen ⟶ NFK - Phenylalanine and tyrosine catabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism:
L-Trp + Oxygen ⟶ NFK - Phenylalanine and tyrosine catabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism:
CARN + SAM ⟶ Anserine + SAH - Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism:
L-Trp + Oxygen ⟶ NFK - Phenylalanine and tyrosine catabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism:
L-Trp + Oxygen ⟶ NFK - Phenylalanine and tyrosine catabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism:
L-Trp + Oxygen ⟶ NFK - Phenylalanine and tyrosine catabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine and tyrosine catabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine metabolism:
4aOH-BH4 ⟶ H2O + qDHB - Phenylalanine and tyrosine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Amino acid and derivative metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA - Amino acid and derivative metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi - Amino acid and derivative metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA - Amino acid and derivative metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA - Amino acid and derivative metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Amino acid and derivative metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Amino acid and derivative metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi - Amino acid and derivative metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA - Amino acid and derivative metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Phenylalanine and tyrosine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV - Phenylalanine metabolism:
H2O + L-Phe + Oxygen ⟶ H2O2 + ammonia + kPPV
BioCyc(14)
- L-phenylalanine degradation III:
2-phenylethanol + NAD+ ⟶ H+ + NADH + phenylacetaldehyde - L-phenylalanine degradation II (anaerobic):
3-phenyl-2-oxopropanoate + H+ ⟶ CO2 + phenylacetaldehyde - L-phenylalanine degradation II (anaerobic):
keto-phenylpyruvate + glu ⟶ 2-oxoglutarate + phe - phenylalanine degradation:
phe + pyruvate ⟶ keto-phenylpyruvate + ala - L-phenylalanine degradation III:
2-phenylethanol + NAD+ ⟶ H+ + NADH + phenylacetaldehyde - phenylalanine degradation III:
phe + pyruvate ⟶ ala + phenylpyruvate - phenylalanine degradation II (anaerobic):
glt + phenylpyruvate ⟶ 2-oxoglutarate + phe - L-phenylalanine degradation II (anaerobic):
H2O + NAD+ + phenylacetaldehyde ⟶ H+ + NADH + phenylacetate - L-phenylalanine degradation II (anaerobic):
2-oxo-3-phenylpropanoate + glt ⟶ 2-oxoglutarate + phe - phenylalanine degradation III:
phe + pyruvate ⟶ ala + phenylpyruvate - phenylalanine degradation III:
phe + pyruvate ⟶ ala + keto-phenylpyruvate - phenylalanine degradation III:
phe + pyruvate ⟶ ala + keto-phenylpyruvate - (-)-microperfuranone biosynthesis:
3-phenyl-2-oxopropanoate + ATP + H2O ⟶ (-)-microperfuranone + AMP + CO2 + diphosphate - phenylalanine degradation II (anaerobic):
glt + phenylpyruvate ⟶ 2-oxoglutarate + phe
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(2)
- L-phenylalanine degradation III:
3-phenyl-2-oxopropanoate + H+ ⟶ CO2 + phenylacetaldehyde - L-phenylalanine degradation III:
2-phenylethanol + NAD+ ⟶ H+ + NADH + phenylacetaldehyde
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
0 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：
- PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。
文献列表
- Anne Jahn, Maike Petersen. Hydroxy(phenyl)pyruvic acid reductase in Actaea racemosa L.: a putative enzyme in cimicifugic and fukinolic acid biosynthesis.
Planta.
2024 Mar; 259(5):102. doi:
10.1007/s00425-024-04382-6. [PMID: 38549005] - Zuanxian Su, Qiushen Xiao, Jiyuan Shen, Houbin Chen, Shijuan Yan, Wenjie Huang. Metabolomics Analysis of Litchi Leaves during Floral Induction Reveals Metabolic Improvement by Stem Girdling.
Molecules (Basel, Switzerland).
2021 Jul; 26(13):. doi:
10.3390/molecules26134048. [PMID: 34279388] - Anne Daly, Sharon Evans, Alex Pinto, Catherine Ashmore, Anita MacDonald. Protein Substitutes in PKU; Their Historical Evolution.
Nutrients.
2021 Feb; 13(2):. doi:
10.3390/nu13020484. [PMID: 33540516] - Kyeongwoo Jang, W Seth Horne, Sanford A Asher. Human Serum Phenylpyruvate Quantification Using Responsive 2D Photonic Crystal Hydrogels via Chemoselective Oxime Ligation: Progress toward Developing Phenylalanine-Sensing Elements.
ACS applied materials & interfaces.
2020 Sep; 12(35):39612-39619. doi:
10.1021/acsami.0c08787. [PMID: 32805910] - Joseph H Lynch, Yichun Qian, Longyun Guo, Itay Maoz, Xing-Qi Huang, Alekzander S Garcia, Gordon Louie, Marianne E Bowman, Joseph P Noel, John A Morgan, Natalia Dudareva. Modulation of auxin formation by the cytosolic phenylalanine biosynthetic pathway.
Nature chemical biology.
2020 08; 16(8):850-856. doi:
10.1038/s41589-020-0519-8. [PMID: 32284603] - Amsha Viraragavan, Nokulunga Hlengwa, Dalene de Beer, Sylvia Riedel, Neil Miller, Sandra Bowles, Beata Walczak, Christo Muller, Elizabeth Joubert. Model development for predicting in vitro bio-capacity of green rooibos extract based on composition for application as screening tool in quality control.
Food & function.
2020 Apr; 11(4):3084-3094. doi:
10.1039/c9fo02480h. [PMID: 32195502] - Yichun Qian, Joseph H Lynch, Longyun Guo, David Rhodes, John A Morgan, Natalia Dudareva. Completion of the cytosolic post-chorismate phenylalanine biosynthetic pathway in plants.
Nature communications.
2019 01; 10(1):15. doi:
10.1038/s41467-018-07969-2. [PMID: 30604768] - Fei Qiu, Chunxian Yang, Lina Yuan, Dan Xiang, Xiaozhong Lan, Min Chen, Zhihua Liao. A Phenylpyruvic Acid Reductase Is Required for Biosynthesis of Tropane Alkaloids.
Organic letters.
2018 12; 20(24):7807-7810. doi:
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1994 Mar; 47(5):821-5. doi:
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Chemical & pharmaceutical bulletin.
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1965; 17(?):260-4. doi:
10.3109/00365516509075345. [PMID: 14320097] - D ALAGILLE, C GENTIL. [CONGENITAL CIRRHOSIS WITH COMPLEX RENAL TUBULE DISEASE DUE TO AN ANOMALY OF TYROSINE METABOLISM].
Revue medico-chirurgicale des maladies du foie.
1964 Dec; 39(?):289-306. doi:
NULL. [PMID: 14245759] - S HALVORSEN, L R GJESSING. STUDIES ON TYROSINOSIS: 1, EFFECT OF LOW-TYROSINE AND LOW-PHENYLALANINE DIET.
British medical journal.
1964 Nov; 2(5418):1171-3. doi:
10.1136/bmj.2.5418.1171. [PMID: 14190487] - A N KVIATKOVSKAIA, A S KAINOVA, I N MIKHAILOVA. [TYROSINE METABOLISM DISORDERS IN PATIENTS WITH COLLAGEN DISEASES. II. 2,5-DIHYDROXYPHENYLPYRUVIC ACID AND ITS CLINICAL SIGNIFICANCE IN COLLAGEN DISEASES].
Terapevticheskii arkhiv.
1964 Oct; 36(?):76-81. doi:
NULL. [PMID: 14309922] - A ALLEGRANZA, E ALDEGHI, P CANEVINI, C DEVITO. [METABOLIC ASPECTS OF PHENYLKETONURIA WITH PARTICULAR ATTENTION TO URINARY ELIMINATION OF SOME PHENOLIC ACIDS].
Minerva pediatrica.
1964 Sep; 16(?):955-61. doi:
NULL. [PMID: 14197271] - W Y WU. CHEMICAL DIAGNOSIS OF PHENYLKETONURIA. REPORT OF 8 CASES.
Chinese medical journal (Peking, China : 1932).
1964 Sep; 83(?):579-86. doi:
NULL. [PMID: 14199833] - S A BERRY, J N CAMPBELL. A RAPID TECHNIQUE FOR THE SEPARATION AND QUANTITATION OF FREE ALPHA-KETO ACIDS IN COMPLEX SOLUTIONS.
Analytical biochemistry.
1964 Aug; 8(?):495-502. doi:
10.1016/0003-2697(64)90247-7. [PMID: 14218916] - R J ALLEN, J L WILSON. URINARY PHENYLPYRUVIC ACID IN PHENYLKETONURIA.
JAMA.
1964 May; 188(?):720-4. doi:
10.1001/jama.1964.03060340018005. [PMID: 14122678] - O L GAMBORG, F J SIMPSON. PREPARATION OF PREPHENIC ACID AND ITS CONVERSION TO PHENYLALANINE AND TYROSINE BY PLANT ENZYMES.
Canadian journal of biochemistry.
1964 May; 42(?):583-91. doi:
10.1139/o64-071. [PMID: 14185725] - R G WHITEHEAD, T R MILBURN. AMINO ACID METABOLISM IN KWASHIORKOR. II. METABOLISM OF PHENYLALANINE AND TYROSINE.
Clinical science.
1964 Apr; 26(?):279-89. doi:
NULL. [PMID: 14161060] - J AKISAWA. [CLINICAL STUDIES ON THE INTERMEDIARY METABOLISM OF TYROSINE. 3. URINARY EXCRETION ON INTERMEDIARY METABOLITES OF TYROSINE IN PATIENTS WITH SOME ENDOCRINE DISEASES AND THE RELATED DISORDERS].
Naika hokan. Japanese archives of internal medicine.
1964 Apr; 11(?):163-72. doi:
NULL. [PMID: 14171676] - J B TU, C C CHEN, T Y LIN, R Q BLACKWELL, Y H CHEN. STUDIES ON PHENYLKETONURIA IN A CHINESE FAMILY.
Zhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui.
1964 Apr; 5(?):56-64. doi:
NULL. [PMID: 14185478] - R HUMBEL. [IDENTIFICATION AND DETERMINATION OF P-HYDROXYPHENYLPYRUVIC ACID AND ITS DERIVATIVES IN URINE].
Das Medizinische Laboratorium.
1964 Mar; 17(?):68-71. doi:
NULL. [PMID: 14193284] - J AKISAWA. [CLINICAL STUDIES ON THE INTERMEDIARY METABOLISM OF TYROSINE. 1. URINARY EXCRETION OF INTERMEDIARY METABOLITES OF TYROSINE IN HEALTHY INDIVIDUALS AND PATIENTS WITH LIVER DISORDERS].
Naika hokan. Japanese archives of internal medicine.
1964 Mar; 11(?):85-95. doi:
NULL. [PMID: 14163645] - J AKISAWA. [CLINICAL STUDIES ON INTERMEDIARY METABOLISM OF TYROSINE. 2. URINARY EXCRETION OF INTERMEDIARY METABOLITES OF TYROSINE IN PATIENTS WITH BLOOD DISORDERS].
Naika hokan. Japanese archives of internal medicine.
1964 Mar; 11(?):97-109. doi:
NULL. [PMID: 14163646] - M M HASSAN. PHENYLKETONURIA IN A SUDANESE FAMILY.
The Journal of pediatrics.
1964 Feb; 64(?):282-4. doi:
10.1016/s0022-3476(64)80275-4. [PMID: 14119530] - S FRITZELL, O R JAGENBURG, L B SCHNUERER. FAMILIAL CIRRHOSIS OF THE LIVER, RENAL TUBULAR DEFECTS WITH RICKETS AND IMPAIRED TYROSINE METABOLISM.
Acta paediatrica.
1964 Jan; 53(?):18-32. doi:
10.1111/j.1651-2227.1964.tb07202.x. [PMID: 14114313] - R ZETTERSTROEM. TYROSINOSIS.
Annals of the New York Academy of Sciences.
1963 Dec; 111(?):220-6. doi:
10.1111/j.1749-6632.1963.tb36962.x. [PMID: 14085846] - J M DAVID. [RECENT KNOWLEDGE ABOUT THE PROBLEM OF PHENYLPYRUVIC OLIGOPHRENIA. FREQUENCY, GENETICS, BIOCHEMISTRY, DIAGNOSIS, AND THERAPEUTICS].
La Semana medica.
1963 Oct; 123(?):1191-206. doi:
NULL. [PMID: 14098630] - C SAUTIER, M PESTEL, F HARDING-GAUDIN, F FAUDEMAY, C FLAMENT. [STUDY OF TRYPTOPHAN METABOLISM IN MAN. APPLICATION TO 2 CASES OF D'EJ'ERINE-SOTTAS DISEASE].
Pathologie et biologie.
1963 Aug; 11(?):908-11. doi:
NULL. [PMID: 14121541] - J DODINVAL-VERSIE. [DETERMINATION OF PHENYLPYRUVIC ACID (PPA) IN THE URINE OF PATIENTS WITH PHENYLPYRUVIC OLIGOPHRENIA (PHENYLKETONURIA)].
Journal de pharmacie de Belgique.
1963 Jul; 18(?):352-65. doi:
NULL. [PMID: 14067935] - R HUMBEL. [Identification and determination of phenylpyruvic acid in the urine].
Medecine et laboratoire.
1963 Jul; 16(?):123-5. doi:
NULL. [PMID: 13955669] - I KRUPANIDHI, B D PUNEKAR. A STUDY OF THE INCIDENCE OF PHENYLKETONURIA IN INDIA.
The Indian journal of medical research.
1963 Jul; 51(?):696-702. doi:
NULL. [PMID: 14073623] - I D WOOTTON. RETENTION OF AROMATIC COMPOUNDS IN ACUTE RENAL FAILURE.
The Scientific basis of medicine annual reviews.
1963; ?(?):235-48. doi:
NULL. [PMID: 14282742] - L CHRISTIAENS, B GAUDIER, B BRIET. [PHENYLKETONURIA. APROPOS OF A FAMILIAL CASE].
Pediatrie.
1963; 18(?):718-21. doi:
NULL. [PMID: 14057985] - F SCHATZ. [Contribution to determination of alpha-keto acids in the urine, with special reference to phenylpyruvic acid].
Wiener klinische Wochenschrift.
1962 Sep; 74(?):630-1. doi:
NULL. [PMID: 13976718] - J W FARQUHAR, E T KANSAS, H P TAIT. Problems of routine screening for phenylketonuria.
Lancet (London, England).
1962 Sep; 2(7254):498-500. doi:
10.1016/s0140-6736(62)90358-6. [PMID: 13891674] - C L VINK. The renal clearance of phenylpyruvate.
Clinica chimica acta; international journal of clinical chemistry.
1961 Nov; 6(?):813-8. doi:
10.1016/0009-8981(61)90170-x. [PMID: 13926107] - A R VEAL. Phenylalanine o-hydroxy-phenylacetic acid phenylpyruvic acid equals phenylketonuric diagnosis. A report of studies made on 77 students in schools for mentally retarded.
The American journal of medical technology.
1961 Jul; 27(?):191-6. doi:
. [PMID: 13780514] - L I WOOLF. Tests for phenylketonuria.
Cerebral palsy bulletin.
1961 Jun; 3(?):249-54. doi:
10.1111/j.1469-8749.1961.tb10376.x. [PMID: 13786634] - de GASQUET, R LOWY, F DECLOITRE. [Effect of adenine nucleotides on the in vitro conversion of D-amino acids. II. Effect of AMP and ATP on phenylpyruvate-L-glutamate transamination in rat kidney homogenates].
Enzymologia biologica et clinica.
1961 196; 1(?):217-24. doi:
NULL. [PMID: 13946745] - P J CHRISTENSEN. A note on the determination of phenylpyruvic acid in urine.
Scandinavian journal of clinical and laboratory investigation.
1961; 13(?):84-6. doi:
10.3109/00365516109137254. [PMID: 13693367] - P FLEURY. [A simplified screening test for phenylpyruvic acid in the urine for a mass survey].
Maandschrift voor kindergeneeskunde.
1960 Dec; 28(?):409-17. doi:
NULL. [PMID: 13700281] - V G ZANNONI, B N LA DU. Tyrosyluria resulting from inhibition of p-hydroxyphenylpyruvic acid oxidase in vitamin C-deficient guinea pigs.
The Journal of biological chemistry.
1960 Sep; 235(?):2667-71. doi:
NULL. [PMID: 13846994] - S SYDNES. [Phenylpyruvic oligophrenia. Detection and semiquantitative determination of phenylpyruvic acid in the urine with the help of phenistix].
Nordisk medicin.
1960 Jul; 64(?):834-6. doi:
NULL. [PMID: 13856398] - S BISAZ. [Determination of phenylalanine and phenylpyruvic acid in the blood and urine. Application to two cases of phenylpyruvic oligophrenia].
Helvetica paediatrica acta.
1959 Sep; 14(?):282-7. doi:
NULL. [PMID: 13800954] - A SAIFER, A F HARRIS. Studies on the photometric determination of phenylpyruvic acid in urine.
Clinical chemistry.
1959 Jun; 5(3):203-17. doi:
10.1093/clinchem/5.3.203. [PMID: 13663273] - de GASQUET, R LOWY, J TREMOLIERES. [Inversion of Damino acids in vitro. Effects of certain factors on the transreamination of phenylpyruvate by a homogenate of rat kidney].
Comptes rendus des seances de la Societe de biologie et de ses filiales.
1959; 153(?):1166-71. doi:
NULL. [PMID: 13826763] - A J SMITH, L B STRANG. An inborn error of metabolism with the urinary excretion of alpha-hydroxy-butyric acid and phenylpyruvic acid.
Archives of disease in childhood.
1958 Apr; 33(168):109-13. doi:
10.1136/adc.33.168.109. [PMID: 13534741] - J VIZET. [Infra-red spectroscopy of phenylpyruvic acid in urine of phenylketonuric patients].
Revue de pathologie generale et de physiologie clinique.
1958 Jan; 58(694):17-23. doi:
NULL. [PMID: 13528428] - A FOLLING, S SYDNES. A method for the estimation of phenylpyruvic acid in urine with some examples of its use in dietary treatment of phenylpyruvic oligophrenia.
Scandinavian journal of clinical and laboratory investigation.
1958; 10(4):355-8. doi:
10.3109/00365515809051236. [PMID: 13615238] - T P THE, P FLEURY, C L VINK. Determination of phenylpyruvic acid in the urine of patients with oligophrenia phenylpyruvica.
Clinica chimica acta; international journal of clinical chemistry.
1957 Oct; 2(5):424-8. doi:
10.1016/0009-8981(57)90039-6. [PMID: 13489879] - J STRODER, E GEISLER. [Influence of fructose on phenylpyruvic acid excretion in phenylpyruvic oligophrenia].
Klinische Wochenschrift.
1957 Jul; 35(14):730. doi:
10.1007/bf01485693. [PMID: 13515052] - W E KNOX, D Y HSIA. Pathogenetic problems in phenylketonuria.
The American journal of medicine.
1957 May; 22(5):687-702. doi:
10.1016/0002-9343(57)90120-1. [PMID: 13410959] - U HENNING, R AMMON. [Excretion of p-hydroxyphenylpyruvic acid, phenylpyruvic acid & other alpha-ketone acids in the urine of healthy humans, also a contribution to the problem of tyrosinosis].
Hoppe-Seyler's Zeitschrift fur physiologische Chemie.
1957 Feb; 306(4-6):221-8. doi:
. [PMID: 13415576] - R AMMON, U HENNING. [Appearance of p-hydroxyphenylpyruvic acid and other alpha-ketone acids in the urine of healthy rabbits and with liver cirrhosis].
Hoppe-Seyler's Zeitschrift fur physiologische Chemie.
1957 Feb; 306(4-6):214-20. doi:
NULL. [PMID: 13415575] - J H JONXIS. Excretion of phenylalanine; report of two cases of phenyl pyruvic acid oligophrenia.
Annales paediatriae Fenniae.
1957; 3(4):555-62. doi:
. [PMID: 13498513] - M D ARMSTRONG, N L LOW. Phenylketonuria VIII. Relation between age, serum phenylalanine level, and phenylpyruvic acid excretion.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.).
1957 Jan; 94(1):142-6. doi:
10.3181/00379727-94-22880. [PMID: 13400895] - H BICKEL. [A form of mental deficiency of metabolic origin].
Deutsches medizinisches Journal.
1956 Jun; 7(11-12):414-6. doi:
NULL. [PMID: 13344233]