Phenylacetaldehyde (BioDeep_00000002899)
Secondary id: BioDeep_00000405604, BioDeep_00000859890
human metabolite PANOMIX_OTCML-2023 Endogenous
代谢物信息卡片
alpha-Phenylacetaldehyde
化学式: C8H8O (120.0575118)
中文名称: 苯乙醛, 苯乙醛
谱图信息:
最多检出来源 Viridiplantae(plant) 0.15%
分子结构信息
SMILES: C1=CC=C(C=C1)CC=O
InChI: InChI=1S/C8H8O/c9-7-6-8-4-2-1-3-5-8/h1-5,7H,6H2
描述信息
Phenylacetaldehyde is one important oxidation-related aldehyde. Exposure to styrene gives phenylacetaldehyde as a secondary metabolite. Styrene has been implicated as reproductive toxicant, neurotoxicant, or carcinogen in vivo or in vitro. Phenylacetaldehyde could be formed by diverse thermal reactions during the cooking process together with C8 compounds is identified as a major aroma- active compound in cooked pine mushroom. Phenylacetaldehyde is readily oxidized to phenylacetic acid. Therefore will eventually be hydrolyzed and oxidized to yield phenylacetic acid that will be excreted primarily in the urine in conjugated form. (PMID: 16910727, 7818768, 15606130).
Found in some essential oils, e.g. Citrus subspecies, Tagetes minuta (Mexican marigold) and in the mushroom Phallus impudicus (common stinkhorn). Flavouring ingredient
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同义名列表
27 个代谢物同义名
alpha-Phenylacetaldehyde; .alpha.-toluic aldehyde; alpha-Toluic aldehyde; Phenylacetic aldehyde; Α-phenylacetaldehyde; 1-oxo-2-Phenylethane; α-Tolyaldehyde; 2-Phenylacetaldehyde; a-Phenylacetaldehyde; α-Tolualdehyde; Benzylcarboxaldehyde; Phenyl-acetaldehyde; Benzeneacetaldehyde; phenylacetaldehyde; alpha-Tolualdehyde; Benzenacetaldehyde; a-Toluic aldehyde; Α-toluic aldehyde; Benzacetaldehyde; Phenacetaldehyde; Oxophenylethane; 2-Phenylethanal; Α-tolualdehyde; a-Tolualdehyde; Phenylethanal; FEMA no. 2974; Hyacinthin
数据库引用编号
20 个数据库交叉引用编号
- ChEBI: CHEBI:16424
- KEGG: C00601
- KEGGdrug: D78329
- PubChem: 998
- HMDB: HMDB0006236
- Metlin: METLIN58372
- DrugBank: DB02178
- ChEMBL: CHEMBL1233464
- Wikipedia: Phenylacetaldehyde
- MetaCyc: PHENYLACETALDEHYDE
- KNApSAcK: C00007535
- foodb: FDB012238
- chemspider: 13876539
- CAS: 122-78-1
- PMhub: MS000006847
- PubChem: 3876
- PDB-CCD: HY1
- 3DMET: B00145
- NIKKAJI: J2.494E
- RefMet: Phenylacetaldehyde
分类词条
相关代谢途径
Reactome(5)
BioCyc(4)
PlantCyc(0)
代谢反应
471 个相关的代谢反应过程信息。
Reactome(57)
- Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA - Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Amine Oxidase reactions:
5HT + H2O + Oxygen ⟶ 5HIALD + H2O2 + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
5HT + H2O + Oxygen ⟶ 5HIALD + H2O2 + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA - Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Amine Oxidase reactions:
5HT + H2O + Oxygen ⟶ 5HIALD + H2O2 + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
5HT + H2O + Oxygen ⟶ 5HIALD + H2O2 + ammonia - Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA - Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Amine Oxidase reactions:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi - Biological oxidations:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN - Phase I - Functionalization of compounds:
CH3CHO + H2O + NAD ⟶ CH3COO- + H+ + NADH - Amine Oxidase reactions:
5HT + H2O + Oxygen ⟶ 5HIALD + H2O2 + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
5HT + H2O + Oxygen ⟶ 5HIALD + H2O2 + ammonia - Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Biological oxidations:
H+ + Oxygen + TPNH + progesterone ⟶ 11DCORST + H2O + TPN - Phase I - Functionalization of compounds:
H+ + Oxygen + TPNH + progesterone ⟶ 11DCORST + H2O + TPN - Amine Oxidase reactions:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA - Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Amine Oxidase reactions:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA - Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Amine Oxidase reactions:
5HT + H2O + Oxygen ⟶ 5HIALD + H2O2 + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
5HT + H2O + Oxygen ⟶ 5HIALD + H2O2 + ammonia - Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA - Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Amine Oxidase reactions:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi - Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Amine Oxidase reactions:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA - Biological oxidations:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN - Phase I - Functionalization of compounds:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN - Amine Oxidase reactions:
5HT + H2O + Oxygen ⟶ 5HIALD + H2O2 + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
5HT + H2O + Oxygen ⟶ 5HIALD + H2O2 + ammonia - Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA - Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN - Amine Oxidase reactions:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia - Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB:
H2O + Oxygen + TYR ⟶ H2O2 + HPHAC + ammonia
BioCyc(31)
- styrene degradation:
(S)-2-phenyloxirane ⟶ phenylacetaldehyde - phenylethylamine degradation I:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethylamine degradation I:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethylamine degradation II:
2-phenylethylamine + A + H2O ⟶ A(H2) + ammonium + phenylacetaldehyde - L-phenylalanine degradation III:
2-phenylethanol + NAD+ ⟶ H+ + NADH + phenylacetaldehyde - L-phenylalanine degradation IV (mammalian, via side chain):
H2O + NAD+ + phenylacetaldehyde ⟶ H+ + NADH + phenylacetate - L-phenylalanine degradation II (anaerobic):
3-phenyl-2-oxopropanoate + H+ ⟶ CO2 + phenylacetaldehyde - superpathway of phenylethylamine degradation:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - superpathway of phenylethylamine degradation:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethylamine degradation I:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + 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 II (anaerobic):
glt + phenylpyruvate ⟶ 2-oxoglutarate + phe - 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 - phenylalanine degradation III:
phe + pyruvate ⟶ ala + keto-phenylpyruvate - phenylethanol biosynthesis:
H2O + O2 + phe ⟶ CO2 + ammonia + hydrogen peroxide + phenylacetaldehyde - L-phenylalanine degradation II (anaerobic):
2-oxo-3-phenylpropanoate + glt ⟶ 2-oxoglutarate + phe - phenylethylamine degradation I:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylalanine degradation III:
phe + pyruvate ⟶ ala + phenylpyruvate - phenylethylamine degradation I:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - superpathway of phenylethylamine degradation:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethylamine degradation I:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H2O + O2 + phe ⟶ CO2 + ammonia + hydrogen peroxide + phenylacetaldehyde - phenylalanine degradation III:
phe + pyruvate ⟶ ala + keto-phenylpyruvate - phenylalanine degradation IV (mammalian, via side chain):
2-phenylethylamine + H2O + O2 ⟶ H+ + ammonia + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H2O + O2 + phe ⟶ CO2 + ammonia + hydrogen peroxide + phenylacetaldehyde
WikiPathways(0)
Plant Reactome(328)
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
NADH + Phenylacetaldehyde ⟶ 2-phenylethanol + NAD - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
phenylpyruvate ⟶ Phenylacetaldehyde + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
H2O + L-Asn ⟶ L-Asp + ammonia - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Amino acid metabolism:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
2OG + L-Val ⟶ Glu + KIV - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
phenylpyruvate ⟶ Phenylacetaldehyde + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
H2O + L-Asn ⟶ L-Asp + ammonia - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
H2O + L-Asn ⟶ L-Asp + ammonia - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Amino acid metabolism:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Amino acid metabolism:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Amino acid catabolism:
2OG + L-Val ⟶ Glu + KIV - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Amino acid metabolism:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Amino acid catabolism:
2OG + L-Val ⟶ Glu + KIV - Ehrlich pathway:
NADH + Phenylacetaldehyde ⟶ 2-phenylethanol + NAD - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
ATP + CoA + propionate ⟶ AMP + PPi + PROP-CoA - Amino acid metabolism:
ATP + CoA + propionate ⟶ AMP + PPi + PROP-CoA - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
L-Phe + PYR ⟶ L-Ala + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Ehrlich pathway:
2OG + L-Phe ⟶ L-Glu + phenylpyruvate
INOH(2)
- Phenylalanine degradation ( Phenylalanine degradation ):
H2O + O2 + Phenyl-ethylamine ⟶ H2O2 + NH3 + Phenyl-acetaldehyde - NAD+ + Phenyl-acetaldehyde + H2O = NADH + Phenyl-acetic acid ( Phenylalanine degradation ):
H2O + NAD+ + Phenyl-acetaldehyde ⟶ NADH + Phenyl-acetic acid
PlantCyc(49)
- phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - L-phenylalanine degradation III:
3-phenyl-2-oxopropanoate + H+ ⟶ CO2 + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - L-phenylalanine degradation III:
2-phenylethanol + NAD+ ⟶ H+ + NADH + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethanol + NAD+ ⟶ H+ + NADH + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
H+ + H2O + O2 + phe ⟶ CO2 + ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde - phenylethanol biosynthesis:
2-phenylethylamine + H2O + O2 ⟶ ammonium + hydrogen peroxide + phenylacetaldehyde
COVID-19 Disease Map(1)
- @COVID-19 Disease
Map["name"]:
2-Methyl-3-acetoacetyl-CoA + Coenzyme A ⟶ Acetyl-CoA + Propanoyl-CoA
PathBank(3)
- Phenylethylamine Metabolism:
Adenosine triphosphate + Coenzyme A + Phenylacetic acid ⟶ Adenosine monophosphate + Phenylacetyl-CoA + Pyrophosphate - Phenylalanine Metabolism:
2-Oxo-3-phenylpropanoic acid (Mixture oxo and keto) + L-Alanine ⟶ L-Phenylalanine + Pyruvic acid - Phenylalanine Metabolism:
2-Oxo-3-phenylpropanoic acid (Mixture oxo and keto) + L-Tyrosine ⟶ 4-Hydroxyphenylpyruvic acid + L-Phenylalanine
PharmGKB(0)
163 个相关的物种来源信息
- 9606 Homo sapiens:
- 329675 Daphne odora: 10.1271/BBB1961.47.483
- 2715869 Daphne papyracea: 10.1271/BBB1961.47.483
- 200489 Saussurea involucrata: 10.1080/10412905.1992.9698080
- 547782 Symphyotrichum undulatum: 10.1021/JF00034A033
- 385370 Aster scaber: 10.1021/JF00034A033
- 4606 Lolium arundinaceum: 10.1016/0031-9422(91)84185-U
- 52153 Festuca rubra: 10.1016/0031-9422(91)84185-U
- 375857 Scolochloa festucacea: 10.1016/0031-9422(91)84185-U
- 114816 Castanopsis cuspidata: 10.1021/JF60224A025
- 328070 Dactylanthus taylorii: 10.1016/0031-9422(95)00403-T
- 4397 Hamamelis virginiana: 10.1055/S-2006-957420
- 29760 Vitis vinifera:
- 65409 Scutellaria baicalensis: 10.1271/BBB1961.51.1449
- 62097 Plumeria rubra:
- 36596 Prunus armeniaca: 10.1021/JF00004A032
- 35924 Paeonia lactiflora:
- 128608 Cinnamomum verum: 10.1021/JF60218A031
- 3661 Cucurbita maxima: 10.1021/JF00073A014
- 85571 Citrus reticulata: 10.1016/J.PHYTOCHEM.2009.07.031
- 558547 Citrus deliciosa: 10.1016/J.PHYTOCHEM.2009.07.031
- 58228 Garcinia mangostana: 10.1016/0031-9422(82)80025-3
- 3635 Gossypium hirsutum: 10.1021/JF60200A011
- 271192 Pimpinella anisum: 10.1016/S0031-9422(98)00022-3
- 41492 Bellis perennis: 10.1016/0031-9422(95)00183-8
- 146781 Phallus impudicus:
- 3755 Prunus dulcis: 10.1021/JF60228A025
- 5315 Ganoderma lucidum: 10.1016/J.PHYTOCHEM.2005.10.025
- 1046361 Fuscopostia leucomallella: 10.1016/J.PHYTOCHEM.2005.10.025
- 155124 Aspalathus linearis: 10.1021/JF00062A024
- 174549 Polygala senega: 10.1002/FFJ.2730100408
- 4577 Zea mays:
- 3039 Euglena gracilis: 10.3389/FBIOE.2021.662655
- 105884 Lonicera japonica: 10.1021/JF950275B
- 137129 Swertia japonica: 10.1246/BCSJ.56.3477
- 3885 Phaseolus vulgaris: 10.1021/JF60199A053
- 114280 Cichorium endivia: 10.1021/JF00068A014
- 3641 Theobroma cacao: 10.1021/JF60160A011
- 4232 Helianthus annuus: 10.1021/JF00123A021
- 79022 Thapsia garganica: 10.1055/S-2006-960216
- 4442 Camellia sinensis: 10.1271/BBB1961.50.1039
- 4217 Arctium lappa: 10.1271/NOGEIKAGAKU1924.59.389
- 7461 Apis cerana: 10.1371/JOURNAL.PONE.0175573
- 661339 Aronia melanocarpa: 10.1002/JSFA.2740360908
- 48119 Glehnia littoralis: 10.1021/JF010219C
- 1548133 Bistorta manshuriensis: 10.1002/CBDV.201100326
- 49827 Glycyrrhiza glabra: 10.1271/NOGEIKAGAKU1924.61.1119
- 205076 Vachellia rigidula: 10.1021/JF00120A008
- 363414 Centaurea armena: 10.1016/J.PHYTOCHEM.2005.04.006
- 5791 Physarum polycephalum: 10.1248/CPB.32.797
- 253513 Marsupella emarginata: 10.1016/S0031-9422(02)00214-5
- 3708 Brassica napus: 10.1016/0031-9422(88)83085-1
- 3711 Brassica rapa: 10.1016/0031-9422(88)83085-1
- 3707 Brassica juncea: 10.1016/0031-9422(88)83085-1
- 3710 Brassica nigra: 10.1016/0031-9422(88)83085-1
- 222877 Phyla nodiflora: 10.1021/NP50039A037
- 4043 Petroselinum crispum: 10.1016/S0031-9422(00)80682-2
- 53737 Sphagneticola trilobata: 10.1002/FFJ.3227
- 261800 Helichrysum pendulum: 10.1055/S-2006-957552
- 1231670 Leiocarpa semicalva: 10.1055/S-2006-957552
- 40145 Tricholoma matsutake:
- 146995 Chrysanthemum indicum: 10.3390/MOLECULES20045346
- 40559 Botrytis cinerea: 10.1248/CPB.31.659
- 38033 Chaetomium globosum: 10.1248/CPB.31.659
- 1000421 Nepeta nepetella: 10.1055/S-2007-969632
- 99501 Echinophora tenuifolia: 10.1080/10412905.1994.9698406
- 97307 Prunus padus: 10.1080/10412905.1990.9697889
- 264418 Hesperis matronalis: 10.1016/0031-9422(94)00332-N
- 58860 Tamarindus indica: 10.1080/10412905.1990.9697860
- 2803977 Aniba canelilla: 10.1080/10412905.1994.9698432
- 4265 Cynara cardunculus: 10.1016/S0031-9422(82)85033-4
- 88149 Saccharina japonica: 10.3390/MOLECULES200712093
- 144042 Pogonomyrmex rugosus: 10.1007/BF00988325
- 1699378 Amauris echeria: 10.1515/ZNC-1988-1-219
- 48597 Truncocolumella citrina: 10.1016/S0305-1978(98)00014-3
- 181713 Tricholoma inamoenum: 10.2307/3807439
- 1840584 Camellia hiemalis: 10.1016/S0031-9422(00)83587-6
- 385388 Camellia oleifera: 10.1016/S0031-9422(00)83587-6
- 182300 Camellia sasanqua: 10.1016/S0031-9422(00)83587-6
- 82025 Hyacinthus orientalis: 10.1016/S0031-9422(00)83587-6
- 4443 Camellia japonica: 10.1016/S0031-9422(00)83587-6
- 9606 Homo sapiens:
- 329675 Daphne odora: 10.1271/BBB1961.47.483
- 2715869 Daphne papyracea: 10.1271/BBB1961.47.483
- 200489 Saussurea involucrata: 10.1080/10412905.1992.9698080
- 547782 Symphyotrichum undulatum: 10.1021/JF00034A033
- 385370 Aster scaber: 10.1021/JF00034A033
- 4606 Lolium arundinaceum: 10.1016/0031-9422(91)84185-U
- 52153 Festuca rubra: 10.1016/0031-9422(91)84185-U
- 375857 Scolochloa festucacea: 10.1016/0031-9422(91)84185-U
- 114816 Castanopsis cuspidata: 10.1021/JF60224A025
- 328070 Dactylanthus taylorii: 10.1016/0031-9422(95)00403-T
- 4397 Hamamelis virginiana: 10.1055/S-2006-957420
- 29760 Vitis vinifera:
- 65409 Scutellaria baicalensis: 10.1271/BBB1961.51.1449
- 62097 Plumeria rubra:
- 36596 Prunus armeniaca: 10.1021/JF00004A032
- 35924 Paeonia lactiflora:
- 128608 Cinnamomum verum: 10.1021/JF60218A031
- 3661 Cucurbita maxima: 10.1021/JF00073A014
- 85571 Citrus reticulata: 10.1016/J.PHYTOCHEM.2009.07.031
- 558547 Citrus deliciosa: 10.1016/J.PHYTOCHEM.2009.07.031
- 58228 Garcinia mangostana: 10.1016/0031-9422(82)80025-3
- 3635 Gossypium hirsutum: 10.1021/JF60200A011
- 271192 Pimpinella anisum: 10.1016/S0031-9422(98)00022-3
- 41492 Bellis perennis: 10.1016/0031-9422(95)00183-8
- 146781 Phallus impudicus:
- 3755 Prunus dulcis: 10.1021/JF60228A025
- 5315 Ganoderma lucidum: 10.1016/J.PHYTOCHEM.2005.10.025
- 1046361 Fuscopostia leucomallella: 10.1016/J.PHYTOCHEM.2005.10.025
- 155124 Aspalathus linearis: 10.1021/JF00062A024
- 174549 Polygala senega: 10.1002/FFJ.2730100408
- 4577 Zea mays:
- 3039 Euglena gracilis: 10.3389/FBIOE.2021.662655
- 105884 Lonicera japonica: 10.1021/JF950275B
- 137129 Swertia japonica: 10.1246/BCSJ.56.3477
- 3885 Phaseolus vulgaris: 10.1021/JF60199A053
- 114280 Cichorium endivia: 10.1021/JF00068A014
- 3641 Theobroma cacao: 10.1021/JF60160A011
- 4232 Helianthus annuus: 10.1021/JF00123A021
- 79022 Thapsia garganica: 10.1055/S-2006-960216
- 4442 Camellia sinensis: 10.1271/BBB1961.50.1039
- 4217 Arctium lappa: 10.1271/NOGEIKAGAKU1924.59.389
- 7461 Apis cerana: 10.1371/JOURNAL.PONE.0175573
- 661339 Aronia melanocarpa: 10.1002/JSFA.2740360908
- 48119 Glehnia littoralis: 10.1021/JF010219C
- 1548133 Bistorta manshuriensis: 10.1002/CBDV.201100326
- 49827 Glycyrrhiza glabra: 10.1271/NOGEIKAGAKU1924.61.1119
- 205076 Vachellia rigidula: 10.1021/JF00120A008
- 363414 Centaurea armena: 10.1016/J.PHYTOCHEM.2005.04.006
- 5791 Physarum polycephalum: 10.1248/CPB.32.797
- 253513 Marsupella emarginata: 10.1016/S0031-9422(02)00214-5
- 3708 Brassica napus: 10.1016/0031-9422(88)83085-1
- 3711 Brassica rapa: 10.1016/0031-9422(88)83085-1
- 3707 Brassica juncea: 10.1016/0031-9422(88)83085-1
- 3710 Brassica nigra: 10.1016/0031-9422(88)83085-1
- 222877 Phyla nodiflora: 10.1021/NP50039A037
- 4043 Petroselinum crispum: 10.1016/S0031-9422(00)80682-2
- 53737 Sphagneticola trilobata: 10.1002/FFJ.3227
- 261800 Helichrysum pendulum: 10.1055/S-2006-957552
- 1231670 Leiocarpa semicalva: 10.1055/S-2006-957552
- 40145 Tricholoma matsutake:
- 146995 Chrysanthemum indicum: 10.3390/MOLECULES20045346
- 40559 Botrytis cinerea: 10.1248/CPB.31.659
- 38033 Chaetomium globosum: 10.1248/CPB.31.659
- 1000421 Nepeta nepetella: 10.1055/S-2007-969632
- 99501 Echinophora tenuifolia: 10.1080/10412905.1994.9698406
- 97307 Prunus padus: 10.1080/10412905.1990.9697889
- 264418 Hesperis matronalis: 10.1016/0031-9422(94)00332-N
- 58860 Tamarindus indica: 10.1080/10412905.1990.9697860
- 2803977 Aniba canelilla: 10.1080/10412905.1994.9698432
- 4265 Cynara cardunculus: 10.1016/S0031-9422(82)85033-4
- 88149 Saccharina japonica: 10.3390/MOLECULES200712093
- 144042 Pogonomyrmex rugosus: 10.1007/BF00988325
- 1699378 Amauris echeria: 10.1515/ZNC-1988-1-219
- 48597 Truncocolumella citrina: 10.1016/S0305-1978(98)00014-3
- 181713 Tricholoma inamoenum: 10.2307/3807439
- 1840584 Camellia hiemalis: 10.1016/S0031-9422(00)83587-6
- 385388 Camellia oleifera: 10.1016/S0031-9422(00)83587-6
- 182300 Camellia sasanqua: 10.1016/S0031-9422(00)83587-6
- 82025 Hyacinthus orientalis: 10.1016/S0031-9422(00)83587-6
- 4443 Camellia japonica: 10.1016/S0031-9422(00)83587-6
- 9606 Homo sapiens: -
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
- Jan Günther, Rayko Halitschke, Jonathan Gershenzon, Meike Burow. Heterologous expression of PtAAS1 reveals the metabolic potential of the common plant metabolite phenylacetaldehyde for auxin synthesis in planta.
Physiologia plantarum.
2023 Nov; 175(6):e14078. doi:
10.1111/ppl.14078. [PMID: 38148231] - Xiaohe Liu, Longfei Shi, Adel Khashaveh, Shuang Shan, Beibei Lv, Shaohua Gu, Yongjun Zhang. Loss of Binding Capabilities in an Ecologically Important Odorant Receptor of the Fall Armyworm, Spodoptera frugiperda, by a Single Point Mutation.
Journal of agricultural and food chemistry.
2023 Aug; ?(?):. doi:
10.1021/acs.jafc.3c04247. [PMID: 37625381] - Sándor Koczor, Miklós Tóth. Field attraction of Eurydema ornata (Hemiptera: Pentatomidae) to allyl isothiocyanate.
Scientific reports.
2023 Jul; 13(1):11063. doi:
10.1038/s41598-023-37705-w. [PMID: 37422493] - Tianyu Yang, Xin Yin, Haotong Kang, Danni Yang, Xingyu Yang, Yunqiang Yang, Yongping Yang. Chromosome-level genome assembly of Murraya paniculata sheds light on biosynthesis of floral volatiles.
BMC biology.
2023 06; 21(1):142. doi:
10.1186/s12915-023-01639-6. [PMID: 37340448] - Xiang Li, Denise Tieman, Saleh Alseekh, Alisdair R Fernie, Harry J Klee. Natural variations in the Sl-AKR9 aldo/keto reductase gene impact fruit flavor volatile and sugar contents.
The Plant journal : for cell and molecular biology.
2023 May; ?(?):. doi:
10.1111/tpj.16310. [PMID: 37243881] - Xinxin Zhang, Xiao Wang, Shiwen Zhao, Kui Fang, Zhun Wang, Jianan Liu, Jinghui Xi, Shang Wang, Juhong Zhang. Response of Odorant Receptors with Phenylacetaldehyde and the Effects on the Behavior of the Rice Water Weevil (Lissorhoptrus oryzophilus).
Journal of agricultural and food chemistry.
2023 May; 71(17):6541-6551. doi:
10.1021/acs.jafc.2c07963. [PMID: 37058441] - Aldo Tava, Elisa Biazzi, Domenico Ronga, Pinarosa Avato. Identification of the Volatile Components of Galium verum L. and Cruciata leavipes Opiz from the Western Italian Alps.
Molecules (Basel, Switzerland).
2020 May; 25(10):. doi:
10.3390/molecules25102333. [PMID: 32429453] - Simone K Huber, Georg Höfner, Klaus T Wanner. Application of the concept of oxime library screening by mass spectrometry (MS) binding assays to pyrrolidine-3-carboxylic acid derivatives as potential inhibitors of γ-aminobutyric acid transporter 1 (GAT1).
Bioorganic & medicinal chemistry.
2019 07; 27(13):2753-2763. doi:
10.1016/j.bmc.2019.05.001. [PMID: 31097402] - Jan Günther, Axel Schmidt, Jonathan Gershenzon, Tobias G Köllner. Phenylacetaldehyde synthase 2 does not contribute to the constitutive formation of 2-phenylethyl-β-D-glucopyranoside in poplar.
Plant signaling & behavior.
2019; 14(11):1668233. doi:
10.1080/15592324.2019.1668233. [PMID: 31532355] - Amarjeet Kumar, Vithal Balavant Kudachikar. Development, characterisation and efficacy evaluation of biochemical fungicidal formulations for postharvest control of anthracnose (Colletotrichum gloeosporioides Penz) disease in mango.
Journal of microencapsulation.
2019 Jan; 36(1):83-95. doi:
10.1080/02652048.2019.1600593. [PMID: 30920322] - Jing Cai, Pengjuan Zu, Florian P Schiestl. The molecular bases of floral scent evolution under artificial selection: insights from a transcriptome analysis in Brassica rapa.
Scientific reports.
2016 11; 6(?):36966. doi:
10.1038/srep36966. [PMID: 27841366] - Francisco J Hidalgo, M Mercedes León, Rosario Zamora. Amino acid decarboxylations produced by lipid-derived reactive carbonyls in amino acid mixtures.
Food chemistry.
2016 Oct; 209(?):256-61. doi:
10.1016/j.foodchem.2016.04.032. [PMID: 27173560] - M Hejazi, M F Movahedi, O Askari, B S Higbee. Novel Chemo-Attractants for Trapping Tomato Leafminer Moth (Lepidoptera: Gelechiidae).
Journal of economic entomology.
2016 10; 109(5):2074-81. doi:
10.1093/jee/tow195. [PMID: 27567219] - Michaela Griesser, Georg Weingart, Katharina Schoedl-Hummel, Nora Neumann, Manuel Becker, Kurt Varmuza, Falk Liebner, Rainer Schuhmacher, Astrid Forneck. Severe drought stress is affecting selected primary metabolites, polyphenols, and volatile metabolites in grapevine leaves (Vitis vinifera cv. Pinot noir).
Plant physiology and biochemistry : PPB.
2015 Mar; 88(?):17-26. doi:
10.1016/j.plaphy.2015.01.004. [PMID: 25602440] - Mahmoud A Omar, Mohamed A Hammad, Dalia M Nagy, Alshymaa A Aly. Development of spectrofluorimetric method for determination of certain aminoglycoside drugs in dosage forms and human plasma through condensation with ninhydrin and phenyl acetaldehyde.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
2015 Feb; 136 Pt C(?):1760-6. doi:
10.1016/j.saa.2014.10.079. [PMID: 25467667] - A C Knauer, F P Schiestl. Bees use honest floral signals as indicators of reward when visiting flowers.
Ecology letters.
2015 Feb; 18(2):135-43. doi:
10.1111/ele.12386. [PMID: 25491788] - Satoshi Nakaya, Atsushi Usami, Tomohito Yorimoto, Mitsuo Miyazawa. Characteristic Chemical Components and Aroma-active Compounds of the Essential Oils from Ranunculus nipponicus var. submersus Used in Japanese Traditional Food.
Journal of oleo science.
2015; 64(6):595-601. doi:
10.5650/jos.ess14265. [PMID: 25891110] - Michael P Torrens-Spence, Renee von Guggenberg, Michael Lazear, Haizhen Ding, Jianyong Li. Diverse functional evolution of serine decarboxylases: identification of two novel acetaldehyde synthases that uses hydrophobic amino acids as substrates.
BMC plant biology.
2014 Sep; 14(?):247. doi:
10.1186/s12870-014-0247-x. [PMID: 25230835] - Anat Levi-Zada, Maayan David, Daniela Fefer, Valeriya Seplyarsky, Avraham Sadowsky, Svetlana Dobrinin, Tamir Ticuchinski, Dafna Harari, Daniel Blumberg, Ezra Dunkelblum. Circadian release of male-specific components of the greater date moth, Aphomia (Arenipses) sabella, using sequential SPME/GC/MS analysis.
Journal of chemical ecology.
2014 Mar; 40(3):236-43. doi:
10.1007/s10886-014-0391-7. [PMID: 24567046] - Sota Nosaka, Mitsuo Miyazawa. Characterization of volatile components and odor-active compounds in the oil of edible mushroom Boletopsis leucomelas.
Journal of oleo science.
2014; 63(6):577-83. doi:
10.5650/jos.ess13215. [PMID: 24881770] - Rosario Zamora, Esmeralda Alcón, Francisco J Hidalgo. Strecker-type degradation of phenylalanine initiated by 4-oxo-2-alkenals in comparison to that initiated by 2,4-alkadienals, 4,5-epoxy-2-alkenals, or 4-hydroxy-2-nonenal.
Journal of agricultural and food chemistry.
2013 Oct; 61(43):10231-7. doi:
10.1021/jf305007y. [PMID: 23360317] - Susan Poehlmann, Peter Schieberle. Characterization of the aroma signature of styrian pumpkin seed oil ( Cucurbita pepo subsp. pepo var. Styriaca) by molecular sensory science.
Journal of agricultural and food chemistry.
2013 Mar; 61(12):2933-42. doi:
10.1021/jf400314j. [PMID: 23461409] - Daihua Hu, Juntao Feng, Zhihui Wang, Hua Wu, Xing Zhang. Effect of nine plant volatiles in the field on the sex pheromones of Leguminivora glycinivorella.
Natural product communications.
2013 Mar; 8(3):393-6. doi:
". [PMID: 23678819] - Pierluigi Caboni, Nadhem Aissani, Tiziana Cabras, Andrea Falqui, Roberto Marotta, Barbara Liori, Nikoletta Ntalli, Giorgia Sarais, Nicola Sasanelli, Graziella Tocco. Potent nematicidal activity of phthalaldehyde, salicylaldehyde, and cinnamic aldehyde against Meloidogyne incognita.
Journal of agricultural and food chemistry.
2013 Feb; 61(8):1794-803. doi:
10.1021/jf305164m. [PMID: 23379671] - Atsuhiko Nakamura, Mitsuo Miyazawa. Evaluation of volatiles from Ampelopsis brevipedunculata var. heterophylla using GC-olfactometry, GC-MS and GC-pulsed flame photometric detector.
Journal of oleo science.
2013; 62(9):645-55. doi:
10.5650/jos.62.645. [PMID: 24005009] - Atsushi Usami, Yusei Kashima, Shinsuke Marumoto, Mitsuo Miyazawa. Characterization of aroma-active compounds in dry flower of Malva sylvestris L. by GC-MS-O analysis and OAV calculations.
Journal of oleo science.
2013; 62(8):563-70. doi:
10.5650/jos.62.563. [PMID: 23985485] - Hanane Moummou, Libert Brice Tonfack, Christian Chervin, Mohamed Benichou, Emmanuel Youmbi, Christian Ginies, Alain Latché, Jean-Claude Pech, Benoît van der Rest. Functional characterization of SlscADH1, a fruit-ripening-associated short-chain alcohol dehydrogenase of tomato.
Journal of plant physiology.
2012 Oct; 169(15):1435-44. doi:
10.1016/j.jplph.2012.06.007. [PMID: 22818888] - Philip E Otienoburu, Babak Ebrahimi, P Larry Phelan, Woodbridge A Foster. Analysis and optimization of a synthetic milkweed floral attractant for mosquitoes.
Journal of chemical ecology.
2012 Jul; 38(7):873-81. doi:
10.1007/s10886-012-0150-6. [PMID: 22711028] - Ahmed M Saveer, Sophie H Kromann, Göran Birgersson, Marie Bengtsson, Tobias Lindblom, Anna Balkenius, Bill S Hansson, Peter Witzgall, Paul G Becher, Rickard Ignell. Floral to green: mating switches moth olfactory coding and preference.
Proceedings. Biological sciences.
2012 Jun; 279(1737):2314-22. doi:
10.1098/rspb.2011.2710. [PMID: 22319127] - Jenny L Wiley, Julie A Marusich, Billy R Martin, John W Huffman. 1-Pentyl-3-phenylacetylindoles and JWH-018 share in vivo cannabinoid profiles in mice.
Drug and alcohol dependence.
2012 Jun; 123(1-3):148-53. doi:
10.1016/j.drugalcdep.2011.11.001. [PMID: 22127210] - Rosario Zamora, Rosa M Delgado, Francisco J Hidalgo. Chemical conversion of phenylethylamine into phenylacetaldehyde by carbonyl-amine reactions in model systems.
Journal of agricultural and food chemistry.
2012 May; 60(21):5491-6. doi:
10.1021/jf301258s. [PMID: 22578256] - Alex Van Moerkercke, Carlos S Galván-Ampudia, Julian C Verdonk, Michel A Haring, Robert C Schuurink. Regulators of floral fragrance production and their target genes in petunia are not exclusively active in the epidermal cells of petals.
Journal of experimental botany.
2012 May; 63(8):3157-71. doi:
10.1093/jxb/ers034. [PMID: 22345641] - Qiu-Hong Pan, Fang Chen, Bao-Qing Zhu, Li-Yan Ma, Li Li, Jing-Ming Li. Molecular cloning and expression of gene encoding aromatic amino acid decarboxylase in 'Vidal blanc' grape berries.
Molecular biology reports.
2012 Apr; 39(4):4319-25. doi:
10.1007/s11033-011-1219-y. [PMID: 21789483] - Hiroshi Hirata, Toshiyuki Ohnishi, Haruka Ishida, Kensuke Tomida, Miwa Sakai, Masakazu Hara, Naoharu Watanabe. Functional characterization of aromatic amino acid aminotransferase involved in 2-phenylethanol biosynthesis in isolated rose petal protoplasts.
Journal of plant physiology.
2012 Mar; 169(5):444-51. doi:
10.1016/j.jplph.2011.12.005. [PMID: 22236980] - Einar J Stauber, Petrissa Kuczka, Maike van Ohlen, Birgit Vogt, Tim Janowitz, Markus Piotrowski, Till Beuerle, Ute Wittstock. Turning the 'mustard oil bomb' into a 'cyanide bomb': aromatic glucosinolate metabolism in a specialist insect herbivore.
PloS one.
2012; 7(4):e35545. doi:
10.1371/journal.pone.0035545. [PMID: 22536404] - Anna Balkenius, Bill Hansson. Discrimination training with multimodal stimuli changes activity in the mushroom body of the hawkmoth Manduca sexta.
PloS one.
2012; 7(4):e32133. doi:
10.1371/journal.pone.0032133. [PMID: 22509244] - Daniela Impellizzeri, Emanuela Esposito, Emanuela Mazzon, Irene Paterniti, Rosanna Di Paola, Valeria Maria Morittu, Antonio Procopio, Domenico Britti, Salvatore Cuzzocrea. Oleuropein aglycone, an olive oil compound, ameliorates development of arthritis caused by injection of collagen type II in mice.
The Journal of pharmacology and experimental therapeutics.
2011 Dec; 339(3):859-69. doi:
10.1124/jpet.111.182808. [PMID: 21880869] - Eunjoo Kim, Hyun-Chul Kim, Se Geun Lee, Sung Jun Lee, Tae-Jung Go, Chul Su Baek, Sang Won Jeong. C-Reactive protein-directed immobilization of phosphocholine ligands on a solid surface.
Chemical communications (Cambridge, England).
2011 Nov; 47(43):11900-2. doi:
10.1039/c1cc15079k. [PMID: 21975508] - Junling Liang, Xiaoji Cao, Jianwei Li, Hongxing Ren, Shihua Wu. [Analysis of volatile components of flowers of Fritillaria thunbergii by GC-TOF-MS].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2011 Oct; 36(19):2689-92. doi:
10.4268/cjcmm20111918. [PMID: 22242431] - Yael Grosjean, Raphael Rytz, Jean-Pierre Farine, Liliane Abuin, Jérôme Cortot, Gregory S X E Jefferis, Richard Benton. An olfactory receptor for food-derived odours promotes male courtship in Drosophila.
Nature.
2011 Sep; 478(7368):236-40. doi:
10.1038/nature10428. [PMID: 21964331] - Nora C Lawo, Georg J F Weingart, Rainer Schuhmacher, Astrid Forneck. The volatile metabolome of grapevine roots: first insights into the metabolic response upon phylloxera attack.
Plant physiology and biochemistry : PPB.
2011 Sep; 49(9):1059-63. doi:
10.1016/j.plaphy.2011.06.008. [PMID: 21764593] - Peiyou Qin, Tingjun Ma, Li Wu, Fang Shan, Guixing Ren. Identification of tartary buckwheat tea aroma compounds with gas chromatography-mass spectrometry.
Journal of food science.
2011 Aug; 76(6):S401-7. doi:
10.1111/j.1750-3841.2011.02223.x. [PMID: 22417522] - Tsuyoshi Goto, Joo-Young Lee, Aki Teraminami, Yong-Il Kim, Shizuka Hirai, Taku Uemura, Hiroyasu Inoue, Nobuyuki Takahashi, Teruo Kawada. Activation of peroxisome proliferator-activated receptor-alpha stimulates both differentiation and fatty acid oxidation in adipocytes.
Journal of lipid research.
2011 May; 52(5):873-84. doi:
10.1194/jlr.m011320. [PMID: 21324916] - Michael Gutensohn, Antje Klempien, Yasuhisa Kaminaga, Dinesh A Nagegowda, Florence Negre-Zakharov, Jung-Hyun Huh, Hongli Luo, Renate Weizbauer, Tesfaye Mengiste, Dorothea Tholl, Natalia Dudareva. Role of aromatic aldehyde synthase in wounding/herbivory response and flower scent production in different Arabidopsis ecotypes.
The Plant journal : for cell and molecular biology.
2011 May; 66(4):591-602. doi:
10.1111/j.1365-313x.2011.04515.x. [PMID: 21284755] - Xiao-Min Chen, Hiromi Kobayashi, Miwa Sakai, Hiroshi Hirata, Tatsuo Asai, Toshiyuki Ohnishi, Susanne Baldermann, Naoharu Watanabe. Functional characterization of rose phenylacetaldehyde reductase (PAR), an enzyme involved in the biosynthesis of the scent compound 2-phenylethanol.
Journal of plant physiology.
2011 Jan; 168(2):88-95. doi:
10.1016/j.jplph.2010.06.011. [PMID: 20650544] - Thomas A Colquhoun, Joo Young Kim, Ashlyn E Wedde, Laura A Levin, Kyle C Schmitt, Robert C Schuurink, David G Clark. PhMYB4 fine-tunes the floral volatile signature of Petunia x hybrida through PhC4H.
Journal of experimental botany.
2011 Jan; 62(3):1133-43. doi:
10.1093/jxb/erq342. [PMID: 21068208] - O Kharoubi, M Slimani, A Aoues. Neuroprotective effect of wormwood against lead exposure.
Journal of emergencies, trauma, and shock.
2011 Jan; 4(1):82-8. doi:
10.4103/0974-2700.76834. [PMID: 21633574] - Ming J Wu, Frank M Clarke, Peter J Rogers, Paul Young, Narelle Sales, Patrick J O'Doherty, Vincent J Higgins. Identification of a protein with antioxidant activity that is important for the protection against beer ageing.
International journal of molecular sciences.
2011; 12(9):6089-103. doi:
10.3390/ijms12096089. [PMID: 22016646] - Mikael A Carlsson, Sonja Bisch-Knaden, Alexander Schäpers, Raimondas Mozuraitis, Bill S Hansson, Niklas Janz. Odour maps in the brain of butterflies with divergent host-plant preferences.
PloS one.
2011; 6(8):e24025. doi:
10.1371/journal.pone.0024025. [PMID: 21901154] - Alisdair R Fernie, Harry J Klee. The use of natural genetic diversity in the understanding of metabolic organization and regulation.
Frontiers in plant science.
2011; 2(?):59. doi:
10.3389/fpls.2011.00059. [PMID: 22645543] - Rajib Saha, Patrick F Suthers, Costas D Maranas. Zea mays iRS1563: a comprehensive genome-scale metabolic reconstruction of maize metabolism.
PloS one.
2011; 6(7):e21784. doi:
10.1371/journal.pone.0021784. [PMID: 21755001] - Christy E Manyi-Loh, Roland N Ndip, Anna M Clarke. Volatile compounds in honey: a review on their involvement in aroma, botanical origin determination and potential biomedical activities.
International journal of molecular sciences.
2011; 12(12):9514-32. doi:
10.3390/ijms12129514. [PMID: 22272147] - Abdolkarim Chehregani, Fariba Mohsenzadeh, Naser Mirazi, Somayeh Hajisadeghian, Zahra Baghali. Chemical composition and antibacterial activity of essential oils of Tripleurospermum disciforme in three developmental stages.
Pharmaceutical biology.
2010 Nov; 48(11):1280-4. doi:
10.3109/13880201003770143. [PMID: 20795784] - Françoise Fons, Didier Froissard, Jean-Marie Bessière, Bruno Buatois, Sylvie Rapior. Biodiversity of volatile organic compounds from five French ferns.
Natural product communications.
2010 Oct; 5(10):1655-8. doi:
". [PMID: 21121267] - Philippe Goffin, Bert van de Bunt, Marco Giovane, Johan H J Leveau, Sachie Höppener-Ogawa, Bas Teusink, Jeroen Hugenholtz. Understanding the physiology of Lactobacillus plantarum at zero growth.
Molecular systems biology.
2010 Sep; 6(?):413. doi:
10.1038/msb.2010.67. [PMID: 20865006] - Toshiyuki Takahashi, Kohji Mizui, Mitsuo Miyazawa. Volatile compounds with characteristic odour in moso-bamboo stems (Phyllostachys pubescens Mazel ex Houz. De ehaie).
Phytochemical analysis : PCA.
2010 Sep; 21(5):489-95. doi:
10.1002/pca.1224. [PMID: 20578110] - Yuhao Ren, Gary Strobel, Joe Sears, Melina Park. Geobacillus sp., a thermophilic soil bacterium producing volatile antibiotics.
Microbial ecology.
2010 Jul; 60(1):130-6. doi:
10.1007/s00248-009-9630-9. [PMID: 20091406] - Jonas M Bengtsson, Satya Prabhakar Chinta, Yitbarek Wolde-Hawariat, Merid Negash, Emiru Seyoum, Bill S Hansson, Fredrik Schlyter, Stefan Schulz, Ylva Hillbur. Pheromone-based mating and aggregation in the sorghum chafer, Pachnoda interrupta.
Journal of chemical ecology.
2010 Jul; 36(7):768-77. doi:
10.1007/s10886-010-9814-2. [PMID: 20549329] - Miklós Tóth, István Szarukán, Béla Dorogi, Attila Gulyás, Pál Nagy, Zoltán Rozgonyi. Male and female noctuid moths attracted to synthetic lures in Europe.
Journal of chemical ecology.
2010 Jun; 36(6):592-8. doi:
10.1007/s10886-010-9789-z. [PMID: 20449640] - Safiyh Taghavi, Daniel van der Lelie, Adam Hoffman, Yian-Biao Zhang, Michael D Walla, Jaco Vangronsveld, Lee Newman, Sébastien Monchy. Genome sequence of the plant growth promoting endophytic bacterium Enterobacter sp. 638.
PLoS genetics.
2010 May; 6(5):e1000943. doi:
10.1371/journal.pgen.1000943. [PMID: 20485560] - Dattatraya G Naik, Hemalata Puntambekar, Priyanka Anantpure. Essential oil of Terminalia chebula fruits as a repellent for the indian honeybee Apis florea.
Chemistry & biodiversity.
2010 May; 7(5):1303-10. doi:
10.1002/cbdv.200900274. [PMID: 20491085] - Amy Marshall Colón, Neelanjan Sengupta, David Rhodes, Natalia Dudareva, John Morgan. A kinetic model describes metabolic response to perturbations and distribution of flux control in the benzenoid network of Petunia hybrida.
The Plant journal : for cell and molecular biology.
2010 Apr; 62(1):64-76. doi:
10.1111/j.1365-313x.2010.04127.x. [PMID: 20070567] - Yichi Xu, Sheryl Barringer. Comparison of tomatillo and tomato volatile compounds in the headspace by selected ion flow tube mass spectrometry (SIFT-MS).
Journal of food science.
2010 Apr; 75(3):C268-73. doi:
10.1111/j.1750-3841.2010.01537.x. [PMID: 20492278] - Lina Yin, Jun'ichi Mano, Shiwen Wang, Wataru Tsuji, Kiyoshi Tanaka. The involvement of lipid peroxide-derived aldehydes in aluminum toxicity of tobacco roots.
Plant physiology.
2010 Mar; 152(3):1406-17. doi:
10.1104/pp.109.151449. [PMID: 20023145] - Moran Farhi, Orly Lavie, Tania Masci, Keren Hendel-Rahmanim, David Weiss, Hagai Abeliovich, Alexander Vainstein. Identification of rose phenylacetaldehyde synthase by functional complementation in yeast.
Plant molecular biology.
2010 Feb; 72(3):235-45. doi:
10.1007/s11103-009-9564-0. [PMID: 19882107] - Itay Gonda, Einat Bar, Vitaly Portnoy, Shery Lev, Joseph Burger, Arthur A Schaffer, Ya'akov Tadmor, Shimon Gepstein, James J Giovannoni, Nurit Katzir, Efraim Lewinsohn. Branched-chain and aromatic amino acid catabolism into aroma volatiles in Cucumis melo L. fruit.
Journal of experimental botany.
2010 Feb; 61(4):1111-23. doi:
10.1093/jxb/erp390. [PMID: 20065117] - Ester Innocent, Cosam C Joseph, Nicholas K Gikonyo, Mayunga H H Nkunya, Ahmed Hassanali. Constituents of the essential oil of Suregada zanzibariensis leaves are repellent to the mosquito, Anopheles gambiae s.s.
Journal of insect science (Online).
2010; 10(?):57. doi:
10.1673/031.010.5701. [PMID: 20569134] - Won Ho Seo, Hyung Hee Baek. Characteristic aroma-active compounds of Korean perilla (Perilla frutescens Britton) leaf.
Journal of agricultural and food chemistry.
2009 Dec; 57(24):11537-42. doi:
10.1021/jf902669d. [PMID: 20000853] - Min Xu, Marc Litaudon, Sabrina Krief, Marie-Thérèse Martin, John Kasenene, Bernard Kiremire, Vincent Dumontet, Françoise Guéritte. Ugandenial A, a new drimane-type sesquiterpenoid from Warburgia ugandensis.
Molecules (Basel, Switzerland).
2009 Sep; 14(10):3844-50. doi:
10.3390/molecules14103844. [PMID: 19924033] - Marc O Waelti, Paul A Page, Alex Widmer, Florian P Schiestl. How to be an attractive male: floral dimorphism and attractiveness to pollinators in a dioecious plant.
BMC evolutionary biology.
2009 Aug; 9(?):190. doi:
10.1186/1471-2148-9-190. [PMID: 19660122] - Christian Abel, Maria Clauss, Andrea Schaub, Jonathan Gershenzon, Dorothea Tholl. Floral and insect-induced volatile formation in Arabidopsis lyrata ssp. petraea, a perennial, outcrossing relative of A. thaliana.
Planta.
2009 Jun; 230(1):1-11. doi:
10.1007/s00425-009-0921-7. [PMID: 19322583] - Ziyin Yang, Miwa Sakai, Hironori Sayama, Taku Shimeno, Koji Yamaguchi, Naoharu Watanabe. Elucidation of the biochemical pathway of 2-phenylethanol from shikimic acid using isolated protoplasts of rose flowers.
Journal of plant physiology.
2009 May; 166(8):887-91. doi:
10.1016/j.jplph.2008.11.001. [PMID: 19097671] - Curtis M Kalua, Paul K Boss. Evolution of volatile compounds during the development of cabernet sauvignon grapes (Vitis vinifera L.).
Journal of agricultural and food chemistry.
2009 May; 57(9):3818-30. doi:
10.1021/jf803471n. [PMID: 19309150] - P Guedes De Pinho, Rui F Gonçalves, Patrícia Valentão, David M Pereira, Rosa M Seabra, Paula B Andrade, Mariana Sottomayor. Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry.
Journal of pharmaceutical and biomedical analysis.
2009 Apr; 49(3):674-85. doi:
10.1016/j.jpba.2008.12.032. [PMID: 19186019] - Miklós Tóth, Ferenc Szentkirályi, József Vuts, Agostino Letardi, Maria Rosaria Tabilio, Gunnhild Jaastad, Geir K Knudsen. Optimization of a phenylacetaldehyde-based attractant for common green lacewings (Chrysoperla carnea s.l.).
Journal of chemical ecology.
2009 Apr; 35(4):449-58. doi:
10.1007/s10886-009-9614-8. [PMID: 19333652] - Akinola O Ogunbinu, Guido Flamini, Pier L Cioni, Muritala A Adebayo, Isiaka A Ogunwande. Constituents of Cajanus cajan (L.) Millsp., Moringa oleifera Lam., Heliotropium indicum L. and Bidens pilosa L. from Nigeria.
Natural product communications.
2009 Apr; 4(4):573-8. doi:
". [PMID: 19476009] - Ming-Fang Wang, Chih-Li Han, Shih-Jiun Yin. Substrate specificity of human and yeast aldehyde dehydrogenases.
Chemico-biological interactions.
2009 Mar; 178(1-3):36-9. doi:
10.1016/j.cbi.2008.10.002. [PMID: 18983993] - Jayne E Rattray, Marc Strous, Huub J M Op den Camp, Stefan Schouten, Mike Sm Jetten, Jaap S Sinninghe Damsté. A comparative genomics study of genetic products potentially encoding ladderane lipid biosynthesis.
Biology direct.
2009 Feb; 4(?):8. doi:
10.1186/1745-6150-4-8. [PMID: 19220888] - Chenxi Zhao, Yingxu Zeng, Mingzhu Wan, Rongxi Li, Yizeng Liang, Chengyong Li, Zhongda Zeng, Foo-Tim Chau. Comparative analysis of essential oils from eight herbal medicines with pungent flavor and cool nature by GC-MS and chemometric resolution methods.
Journal of separation science.
2009 Feb; 32(4):660-70. doi:
10.1002/jssc.200800484. [PMID: 19212980] - Jacquelyn L Blackmer, John A Byers. Lygus spp. (Heteroptera: Miridae) host-plant interactions with Lesquerella fendleri (Brassicaceae), a new crop in the arid southwest.
Environmental entomology.
2009 Feb; 38(1):159-67. doi:
10.1603/022.038.0120. [PMID: 19791610] - Sandrine Mathieu, Valeriano Dal Cin, Zhangjun Fei, Hua Li, Peter Bliss, Mark G Taylor, Harry J Klee, Denise M Tieman. Flavour compounds in tomato fruits: identification of loci and potential pathways affecting volatile composition.
Journal of experimental botany.
2009; 60(1):325-37. doi:
10.1093/jxb/ern294. [PMID: 19088332] - Lloyd D Stringer, Ashraf M El-Sayed, Lyn M Cole, Lee-Anne M Manning, David M Suckling. Floral attractants for the female soybean looper, Thysanoplusia orichalcea (Lepidoptera: Noctuidae).
Pest management science.
2008 Dec; 64(12):1218-21. doi:
10.1002/ps.1621. [PMID: 18615789] - Qianli Wang, Sandamali Amarasingha Ekanayaka, Jian Wu, Junping Zhang, Zhongwu Guo. Synthetic and immunological studies of 5'-N-phenylacetyl sTn to develop carbohydrate-based cancer vaccines and to explore the impacts of linkage between carbohydrate antigens and carrier proteins.
Bioconjugate chemistry.
2008 Oct; 19(10):2060-7. doi:
10.1021/bc800243f. [PMID: 18816108] - Rosario Zamora, Emerenciana Gallardo, Francisco J Hidalgo. Model studies on the degradation of phenylalanine initiated by lipid hydroperoxides and their secondary and tertiary oxidation products.
Journal of agricultural and food chemistry.
2008 Sep; 56(17):7970-5. doi:
10.1021/jf801409w. [PMID: 18707112] - Emerenciana Gallardo, David P De Schutter, Rosario Zamora, Guy Derdelinckx, Freddy R Delvaux, Francisco J Hidalgo. Influence of lipids in the generation of phenylacetaldehyde in wort-related model systems.
Journal of agricultural and food chemistry.
2008 May; 56(9):3155-9. doi:
10.1021/jf800094k. [PMID: 18386901] - Sonia Ventanas, Mario Estevez, Ana I Andrés, Jorge Ruiz. Analysis of volatile compounds of Iberian dry-cured loins with different intramuscular fat contents using SPME-DED.
Meat science.
2008 May; 79(1):172-80. doi:
10.1016/j.meatsci.2007.08.011. [PMID: 22062610] - H Song, K R Cadwallader. Aroma components of American country ham.
Journal of food science.
2008 Jan; 73(1):C29-35. doi:
10.1111/j.1750-3841.2007.00593.x. [PMID: 18211346] - M O Waelti, J K Muhlemann, A Widmer, F P Schiestl. Floral odour and reproductive isolation in two species of Silene.
Journal of evolutionary biology.
2008 Jan; 21(1):111-121. doi:
10.1111/j.1420-9101.2007.01461.x. [PMID: 18031491] - Umma Salma Jhumur, Stefan Dötterl, Andreas Jürgens. Floral odors of Silene otites: their variability and attractiveness to mosquitoes.
Journal of chemical ecology.
2008 Jan; 34(1):14-25. doi:
10.1007/s10886-007-9392-0. [PMID: 18057987] - Eleftherios Alissandrakis, Petros A Tarantilis, Paschalis C Harizanis, Moschos Polissiou. Comparison of the volatile composition in thyme honeys from several origins in Greece.
Journal of agricultural and food chemistry.
2007 Oct; 55(20):8152-7. doi:
10.1021/jf071442y. [PMID: 17824662] - Małgorzata A Majcher, Henryk H Jeleń. Effect of cysteine and cystine addition on sensory profile and potent odorants of extruded potato snacks.
Journal of agricultural and food chemistry.
2007 Jul; 55(14):5754-60. doi:
10.1021/jf0703147. [PMID: 17567142] - Elinor Scott, Francisc Peter, Johan Sanders. Biomass in the manufacture of industrial products--the use of proteins and amino acids.
Applied microbiology and biotechnology.
2007 Jun; 75(4):751-62. doi:
10.1007/s00253-007-0932-x. [PMID: 17387469] - Arporn Jarunrattanasri, Chockchai Theerakulkait, Keith R Cadwallader. Aroma components of acid-hydrolyzed vegetable protein made by partial hydrolysis of rice bran protein.
Journal of agricultural and food chemistry.
2007 Apr; 55(8):3044-50. doi:
10.1021/jf0631474. [PMID: 17367160] - Hiromichi Minami, Emilyn Dubouzet, Kinuko Iwasa, Fumihiko Sato. Functional analysis of norcoclaurine synthase in Coptis japonica.
The Journal of biological chemistry.
2007 Mar; 282(9):6274-82. doi:
10.1074/jbc.m608933200. [PMID: 17204481] - Rosario Zamora, Emerenciana Gallardo, Francisco J Hidalgo. Strecker degradation of phenylalanine initiated by 2,4-decadienal or methyl 13-oxooctadeca-9,11-dienoate in model systems.
Journal of agricultural and food chemistry.
2007 Feb; 55(4):1308-14. doi:
10.1021/jf062838x. [PMID: 17300152] - Umma Salma Jhumur, Stefan Dötterl, Andreas Jürgens. Naive and conditioned responses of Culex pipiens pipiens biotype molestus (Diptera: Culicidae) to flower odors.
Journal of medical entomology.
2006 Nov; 43(6):1164-70. doi:
. [PMID: 17162948] - Yasuhisa Kaminaga, Jennifer Schnepp, Greg Peel, Christine M Kish, Gili Ben-Nissan, David Weiss, Irina Orlova, Orly Lavie, David Rhodes, Karl Wood, D Marshall Porterfield, Arthur J L Cooper, John V Schloss, Eran Pichersky, Alexander Vainstein, Natalia Dudareva. Plant phenylacetaldehyde synthase is a bifunctional homotetrameric enzyme that catalyzes phenylalanine decarboxylation and oxidation.
The Journal of biological chemistry.
2006 Aug; 281(33):23357-66. doi:
10.1074/jbc.m602708200. [PMID: 16766535] - Rosario Zamora, José L Navarro, Emerenciana Gallardo, Francisco J Hidalgo. Chemical conversion of alpha-amino acids into alpha-keto acids by 4,5-epoxy-2-decenal.
Journal of agricultural and food chemistry.
2006 Aug; 54(16):6101-5. doi:
10.1021/jf061239n. [PMID: 16881723] - Lucia Castro-Vázquez, M Consuelo Díaz-Maroto, M Soledad Pérez-Coello. Volatile composition and contribution to the aroma of spanish honeydew honeys. Identification of a new chemical marker.
Journal of agricultural and food chemistry.
2006 Jun; 54(13):4809-13. doi:
10.1021/jf0604384. [PMID: 16787032]