Record Information |
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Version | 5.0 |
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Status | Detected and Quantified |
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Creation Date | 2005-11-16 15:48:42 UTC |
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Update Date | 2023-05-30 20:56:02 UTC |
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HMDB ID | HMDB0000214 |
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Secondary Accession Numbers | - HMDB0000818
- HMDB0004984
- HMDB00214
- HMDB00818
- HMDB04984
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Metabolite Identification |
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Common Name | Ornithine |
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Description | Ornithine or L-ornithine, also known as (S)-2,5-diaminopentanoic acid is a member of the class of compounds known as L-alpha-amino acids. L-alpha-amino acids are alpha amino acids which have the L-configuration of the alpha-carbon atom. L-ornithine is soluble (in water) and a moderately basic compound. Ornithine is a non-proteinogenic amino acid that plays a role in the urea cycle. It is considered to be a non-essential amino acid. A non-essential amino acid is an amino acid that can be synthesized from central metabolic pathway intermediates in humans and is not required in the diet. L-Ornithine is one of the products of the action of the enzyme arginase on L-arginine, creating urea. Therefore, ornithine is a central part of the urea cycle, which allows for the disposal of excess nitrogen. Outside the human body, L-ornithine is abundant in a number of food items such as wild rice, brazil nuts, common oregano, and common grapes. L-ornithine can be found throughout most human tissues; and in most biofluids, some of which include blood, urine, cerebrospinal fluid (CSF), sweat, saliva, and feces. L-ornithine exists in all living species, from bacteria to plants to humans. L-Ornithine is also a precursor of citrulline and arginine. In order for ornithine that is produced in the cytosol to be converted to citrulline, it must first cross the inner mitochondrial membrane into the mitochondrial matrix where it is carbamylated by the enzyme known as ornithine transcarbamylase. This transfer is mediated by the mitochondrial ornithine transporter (SLC25A15; AF112968; ORNT1). Mutations in the mitochondrial ornithine transporter result in hyperammonemia, hyperornithinemia, homocitrullinuria (HHH) syndrome, a disorder of the urea cycle (PMID: 16256388 ). The pathophysiology of the disease may involve diminished ornithine transport into mitochondria, resulting in ornithine accumulation in the cytoplasm and reduced ability to clear carbamoyl phosphate and ammonia loads (OMIM 838970 ). In humans, L-ornithine is involved in a number of other metabolic disorders, some of which include, ornithine transcarbamylase deficiency (OTC deficiency), argininemia, and guanidinoacetate methyltransferase deficiency (GAMT deficiency). Ornithine is abnormally accumulated in the body in ornithine transcarbamylase deficiency. Moreover, Ornithine is found to be associated with cystinuria, hyperdibasic aminoaciduria I, and lysinuric protein intolerance, which are inborn errors of metabolism. It has been claimed that ornithine improves athletic performance, has anabolic effects, has wound-healing effects, and is immuno-enhancing. |
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Structure | InChI=1S/C5H12N2O2/c6-3-1-2-4(7)5(8)9/h4H,1-3,6-7H2,(H,8,9)/t4-/m0/s1 |
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Synonyms | Value | Source |
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(S)-2,5-Diaminopentanoate | ChEBI | (S)-2,5-Diaminopentanoic acid | ChEBI | (S)-2,5-Diaminovaleric acid | ChEBI | (S)-alpha,delta-Diaminovaleric acid | ChEBI | (S)-Ornithine | ChEBI | (S)-2,5-Diaminovalerate | Generator | (S)-a,delta-Diaminovalerate | Generator | (S)-a,delta-Diaminovaleric acid | Generator | (S)-alpha,delta-Diaminovalerate | Generator | (S)-Α,δ-diaminovalerate | Generator | (S)-Α,δ-diaminovaleric acid | Generator | (S)-a,Δ-diaminovalerate | HMDB | (S)-a,Δ-diaminovaleric acid | HMDB | (+)-S-Ornithine | HMDB | (S)-a,D-Diaminovalerate | HMDB | (S)-a,D-Diaminovaleric acid | HMDB | 5-Amino-L-norvaline | HMDB | L-(-)-Ornithine | HMDB | L-Ornithine | HMDB | 2,5-Diaminopentanoic acid | HMDB | Ornithine dihydrochloride, (L)-isomer | HMDB | Ornithine hydrochloride, (D)-isomer | HMDB | Ornithine, (D)-isomer | HMDB | Ornithine, (L)-isomer | HMDB | 2,5 Diaminopentanoic acid | HMDB | Ornithine monoacetate, (L)-isomer | HMDB | Ornithine monohydrochloride, (D)-isomer | HMDB | Ornithine monohydrochloride, (DL)-isomer | HMDB | Ornithine phosphate (1:1), (L)-isomer | HMDB | Ornithine sulfate (1:1), (L)-isomer | HMDB | Ornithine hydrochloride, (DL)-isomer | HMDB | Ornithine hydrochloride, (L)-isomer | HMDB | Ornithine monohydrobromide, (L)-isomer | HMDB | Ornithine, (DL)-isomer | HMDB |
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Chemical Formula | C5H12N2O2 |
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Average Molecular Weight | 132.161 |
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Monoisotopic Molecular Weight | 132.089877638 |
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IUPAC Name | (2S)-2,5-diaminopentanoic acid |
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Traditional Name | ornithine |
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CAS Registry Number | 3184-13-2 |
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SMILES | NCCC[C@H](N)C(O)=O |
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InChI Identifier | InChI=1S/C5H12N2O2/c6-3-1-2-4(7)5(8)9/h4H,1-3,6-7H2,(H,8,9)/t4-/m0/s1 |
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InChI Key | AHLPHDHHMVZTML-BYPYZUCNSA-N |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. |
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Kingdom | Organic compounds |
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Super Class | Organic acids and derivatives |
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Class | Carboxylic acids and derivatives |
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Sub Class | Amino acids, peptides, and analogues |
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Direct Parent | L-alpha-amino acids |
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Alternative Parents | |
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Substituents | - L-alpha-amino acid
- Fatty acid
- Amino acid
- Carboxylic acid
- Monocarboxylic acid or derivatives
- Amine
- Hydrocarbon derivative
- Organic oxide
- Organopnictogen compound
- Primary amine
- Organooxygen compound
- Organonitrogen compound
- Organic oxygen compound
- Primary aliphatic amine
- Organic nitrogen compound
- Carbonyl group
- Aliphatic acyclic compound
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Molecular Framework | Aliphatic acyclic compounds |
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External Descriptors | |
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Ontology |
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Physiological effect | Not Available |
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Disposition | |
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Process | |
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Role | |
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Physical Properties |
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State | Solid |
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Experimental Molecular Properties | Property | Value | Reference |
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Melting Point | 140 °C | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | 620 mg/mL | Not Available | LogP | -4.22 | SANGSTER (1994) |
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Experimental Chromatographic Properties | Experimental Collision Cross Sections |
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Predicted Molecular Properties | |
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Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Kovats Retention IndicesUnderivatizedDerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
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Ornithine,1TMS,isomer #1 | C[Si](C)(C)OC(=O)[C@@H](N)CCCN | 1369.7 | Semi standard non polar | 33892256 | Ornithine,1TMS,isomer #2 | C[Si](C)(C)NCCC[C@H](N)C(=O)O | 1525.7 | Semi standard non polar | 33892256 | Ornithine,1TMS,isomer #3 | C[Si](C)(C)N[C@@H](CCCN)C(=O)O | 1479.8 | Semi standard non polar | 33892256 | Ornithine,2TMS,isomer #1 | C[Si](C)(C)N[C@@H](CCCN)C(=O)O[Si](C)(C)C | 1475.8 | Semi standard non polar | 33892256 | Ornithine,2TMS,isomer #1 | C[Si](C)(C)N[C@@H](CCCN)C(=O)O[Si](C)(C)C | 1570.4 | Standard non polar | 33892256 | Ornithine,2TMS,isomer #1 | C[Si](C)(C)N[C@@H](CCCN)C(=O)O[Si](C)(C)C | 2210.7 | Standard polar | 33892256 | Ornithine,2TMS,isomer #2 | C[Si](C)(C)NCCC[C@H](N)C(=O)O[Si](C)(C)C | 1521.1 | Semi standard non polar | 33892256 | Ornithine,2TMS,isomer #2 | C[Si](C)(C)NCCC[C@H](N)C(=O)O[Si](C)(C)C | 1634.2 | Standard non polar | 33892256 | Ornithine,2TMS,isomer #2 | C[Si](C)(C)NCCC[C@H](N)C(=O)O[Si](C)(C)C | 2225.8 | Standard polar | 33892256 | Ornithine,2TMS,isomer #3 | C[Si](C)(C)NCCC[C@H](N[Si](C)(C)C)C(=O)O | 1627.3 | Semi standard non polar | 33892256 | Ornithine,2TMS,isomer #3 | C[Si](C)(C)NCCC[C@H](N[Si](C)(C)C)C(=O)O | 1637.6 | Standard non polar | 33892256 | Ornithine,2TMS,isomer #3 | C[Si](C)(C)NCCC[C@H](N[Si](C)(C)C)C(=O)O | 2143.0 | Standard polar | 33892256 | Ornithine,2TMS,isomer #4 | C[Si](C)(C)N(CCC[C@H](N)C(=O)O)[Si](C)(C)C | 1748.7 | Semi standard non polar | 33892256 | Ornithine,2TMS,isomer #4 | C[Si](C)(C)N(CCC[C@H](N)C(=O)O)[Si](C)(C)C | 1667.5 | Standard non polar | 33892256 | Ornithine,2TMS,isomer #4 | C[Si](C)(C)N(CCC[C@H](N)C(=O)O)[Si](C)(C)C | 2661.8 | Standard polar | 33892256 | Ornithine,2TMS,isomer #5 | C[Si](C)(C)N([C@@H](CCCN)C(=O)O)[Si](C)(C)C | 1629.3 | Semi standard non polar | 33892256 | Ornithine,2TMS,isomer #5 | C[Si](C)(C)N([C@@H](CCCN)C(=O)O)[Si](C)(C)C | 1592.2 | Standard non polar | 33892256 | Ornithine,2TMS,isomer #5 | C[Si](C)(C)N([C@@H](CCCN)C(=O)O)[Si](C)(C)C | 2362.3 | Standard polar | 33892256 | Ornithine,3TMS,isomer #1 | C[Si](C)(C)NCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C | 1623.6 | Semi standard non polar | 33892256 | Ornithine,3TMS,isomer #1 | C[Si](C)(C)NCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C | 1744.0 | Standard non polar | 33892256 | Ornithine,3TMS,isomer #1 | C[Si](C)(C)NCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C | 1804.3 | Standard polar | 33892256 | Ornithine,3TMS,isomer #2 | C[Si](C)(C)OC(=O)[C@H](CCCN)N([Si](C)(C)C)[Si](C)(C)C | 1672.5 | Semi standard non polar | 33892256 | Ornithine,3TMS,isomer #2 | C[Si](C)(C)OC(=O)[C@H](CCCN)N([Si](C)(C)C)[Si](C)(C)C | 1698.9 | Standard non polar | 33892256 | Ornithine,3TMS,isomer #2 | C[Si](C)(C)OC(=O)[C@H](CCCN)N([Si](C)(C)C)[Si](C)(C)C | 2101.5 | Standard polar | 33892256 | Ornithine,3TMS,isomer #3 | C[Si](C)(C)OC(=O)[C@@H](N)CCCN([Si](C)(C)C)[Si](C)(C)C | 1741.7 | Semi standard non polar | 33892256 | Ornithine,3TMS,isomer #3 | C[Si](C)(C)OC(=O)[C@@H](N)CCCN([Si](C)(C)C)[Si](C)(C)C | 1792.4 | Standard non polar | 33892256 | Ornithine,3TMS,isomer #3 | C[Si](C)(C)OC(=O)[C@@H](N)CCCN([Si](C)(C)C)[Si](C)(C)C | 2148.9 | Standard polar | 33892256 | Ornithine,3TMS,isomer #4 | C[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O | 1832.5 | Semi standard non polar | 33892256 | Ornithine,3TMS,isomer #4 | C[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O | 1774.5 | Standard non polar | 33892256 | Ornithine,3TMS,isomer #4 | C[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O | 2041.1 | Standard polar | 33892256 | Ornithine,3TMS,isomer #5 | C[Si](C)(C)NCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C | 1785.9 | Semi standard non polar | 33892256 | Ornithine,3TMS,isomer #5 | C[Si](C)(C)NCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C | 1764.1 | Standard non polar | 33892256 | Ornithine,3TMS,isomer #5 | C[Si](C)(C)NCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C | 1949.7 | Standard polar | 33892256 | Ornithine,4TMS,isomer #1 | C[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C | 1820.3 | Semi standard non polar | 33892256 | Ornithine,4TMS,isomer #1 | C[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C | 1850.6 | Standard non polar | 33892256 | Ornithine,4TMS,isomer #1 | C[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C | 1792.8 | Standard polar | 33892256 | Ornithine,4TMS,isomer #2 | C[Si](C)(C)NCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C | 1791.2 | Semi standard non polar | 33892256 | Ornithine,4TMS,isomer #2 | C[Si](C)(C)NCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C | 1855.4 | Standard non polar | 33892256 | Ornithine,4TMS,isomer #2 | C[Si](C)(C)NCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C | 1754.0 | Standard polar | 33892256 | Ornithine,4TMS,isomer #3 | C[Si](C)(C)N(CCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C | 1975.3 | Semi standard non polar | 33892256 | Ornithine,4TMS,isomer #3 | C[Si](C)(C)N(CCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C | 1900.5 | Standard non polar | 33892256 | Ornithine,4TMS,isomer #3 | C[Si](C)(C)N(CCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C | 1923.8 | Standard polar | 33892256 | Ornithine,5TMS,isomer #1 | C[Si](C)(C)OC(=O)[C@H](CCCN([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C | 2049.1 | Semi standard non polar | 33892256 | Ornithine,5TMS,isomer #1 | C[Si](C)(C)OC(=O)[C@H](CCCN([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C | 1961.7 | Standard non polar | 33892256 | Ornithine,5TMS,isomer #1 | C[Si](C)(C)OC(=O)[C@H](CCCN([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C | 1759.3 | Standard polar | 33892256 | Ornithine,1TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCN | 1600.5 | Semi standard non polar | 33892256 | Ornithine,1TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)NCCC[C@H](N)C(=O)O | 1785.9 | Semi standard non polar | 33892256 | Ornithine,1TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)N[C@@H](CCCN)C(=O)O | 1729.7 | Semi standard non polar | 33892256 | Ornithine,2TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)N[C@@H](CCCN)C(=O)O[Si](C)(C)C(C)(C)C | 1964.4 | Semi standard non polar | 33892256 | Ornithine,2TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)N[C@@H](CCCN)C(=O)O[Si](C)(C)C(C)(C)C | 1967.2 | Standard non polar | 33892256 | Ornithine,2TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)N[C@@H](CCCN)C(=O)O[Si](C)(C)C(C)(C)C | 2274.0 | Standard polar | 33892256 | Ornithine,2TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)NCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C | 1986.6 | Semi standard non polar | 33892256 | Ornithine,2TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)NCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C | 2036.4 | Standard non polar | 33892256 | Ornithine,2TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)NCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C | 2309.0 | Standard polar | 33892256 | Ornithine,2TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)NCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O | 2128.2 | Semi standard non polar | 33892256 | Ornithine,2TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)NCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O | 2022.6 | Standard non polar | 33892256 | Ornithine,2TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)NCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O | 2230.0 | Standard polar | 33892256 | Ornithine,2TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)N(CCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C | 2177.6 | Semi standard non polar | 33892256 | Ornithine,2TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)N(CCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C | 2078.8 | Standard non polar | 33892256 | Ornithine,2TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)N(CCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C | 2578.9 | Standard polar | 33892256 | Ornithine,2TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)N([C@@H](CCCN)C(=O)O)[Si](C)(C)C(C)(C)C | 2064.3 | Semi standard non polar | 33892256 | Ornithine,2TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)N([C@@H](CCCN)C(=O)O)[Si](C)(C)C(C)(C)C | 2002.8 | Standard non polar | 33892256 | Ornithine,2TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)N([C@@H](CCCN)C(=O)O)[Si](C)(C)C(C)(C)C | 2332.3 | Standard polar | 33892256 | Ornithine,3TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)NCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C | 2276.6 | Semi standard non polar | 33892256 | Ornithine,3TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)NCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C | 2287.0 | Standard non polar | 33892256 | Ornithine,3TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)NCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C | 2164.2 | Standard polar | 33892256 | Ornithine,3TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCN)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2345.8 | Semi standard non polar | 33892256 | Ornithine,3TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCN)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2278.6 | Standard non polar | 33892256 | Ornithine,3TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCN)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2290.5 | Standard polar | 33892256 | Ornithine,3TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2390.3 | Semi standard non polar | 33892256 | Ornithine,3TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2377.4 | Standard non polar | 33892256 | Ornithine,3TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2347.9 | Standard polar | 33892256 | Ornithine,3TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O | 2508.0 | Semi standard non polar | 33892256 | Ornithine,3TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O | 2342.2 | Standard non polar | 33892256 | Ornithine,3TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O | 2294.4 | Standard polar | 33892256 | Ornithine,3TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)NCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2477.7 | Semi standard non polar | 33892256 | Ornithine,3TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)NCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2323.5 | Standard non polar | 33892256 | Ornithine,3TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)NCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2232.9 | Standard polar | 33892256 | Ornithine,4TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C | 2680.1 | Semi standard non polar | 33892256 | Ornithine,4TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C | 2568.7 | Standard non polar | 33892256 | Ornithine,4TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)N[C@@H](CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C | 2258.5 | Standard polar | 33892256 | Ornithine,4TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)NCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2688.3 | Semi standard non polar | 33892256 | Ornithine,4TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)NCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2553.2 | Standard non polar | 33892256 | Ornithine,4TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)NCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2233.1 | Standard polar | 33892256 | Ornithine,4TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)N(CCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2813.9 | Semi standard non polar | 33892256 | Ornithine,4TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)N(CCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2626.9 | Standard non polar | 33892256 | Ornithine,4TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)N(CCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2303.3 | Standard polar | 33892256 | Ornithine,5TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 3056.3 | Semi standard non polar | 33892256 | Ornithine,5TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2818.2 | Standard non polar | 33892256 | Ornithine,5TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C | 2312.3 | Standard polar | 33892256 |
|
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| GC-MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
---|
Experimental GC-MS | GC-MS Spectrum - Ornithine GC-EI-TOF (Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies) (2 TMS) | splash10-0006-1920000000-b0357b8c9888abda7d80 | 2014-06-16 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-EI-TOF (Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies) (Non-derivatized) | splash10-0006-0910000000-8aaa0faabf1429b90611 | 2014-06-16 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-EI-TOF (Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies) (2 TMS) | splash10-00di-7910000000-5fa118444ceb45204aa3 | 2014-06-16 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-MS (3 TMS) | splash10-006x-3910000000-f6d0c6492f2cab33a392 | 2014-06-16 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-MS (3 TMS) | splash10-00dr-2900000000-77222ff2d0118d3d3b57 | 2014-06-16 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-MS (4 TMS) | splash10-0006-1910000000-53c73c4fa3665c44d3b9 | 2014-06-16 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-MS (5 TMS) | splash10-03di-1691000000-dc14976cfee86cc828b9 | 2014-06-16 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine EI-B (Non-derivatized) | splash10-0006-0920000000-f65f61e4a3739eabb1d1 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-EI-TOF (Non-derivatized) | splash10-0006-1920000000-b0357b8c9888abda7d80 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-EI-TOF (Non-derivatized) | splash10-0006-0910000000-8aaa0faabf1429b90611 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-EI-TOF (Non-derivatized) | splash10-00di-7910000000-5fa118444ceb45204aa3 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-MS (Non-derivatized) | splash10-006x-3910000000-f6d0c6492f2cab33a392 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-MS (Non-derivatized) | splash10-00dr-2900000000-77222ff2d0118d3d3b57 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-MS (Non-derivatized) | splash10-0006-1910000000-53c73c4fa3665c44d3b9 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-MS (Non-derivatized) | splash10-03di-1691000000-dc14976cfee86cc828b9 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-EI-TOF (Non-derivatized) | splash10-0006-0900000000-f59681b9f46f1b738487 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-EI-TOF (Non-derivatized) | splash10-0006-0900000000-3048477975b51ae176af | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-EI-TOF (Non-derivatized) | splash10-00dr-2900000000-8d1a2cc0a88f7d9216e1 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Experimental GC-MS | GC-MS Spectrum - Ornithine GC-EI-TOF (Non-derivatized) | splash10-0udi-1900000000-bc40b76e8b03ef7a08f0 | 2017-09-12 | HMDB team, MONA, MassBank | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Ornithine GC-MS (Non-derivatized) - 70eV, Positive | splash10-001l-9000000000-50fe14c2cb68fd09e32f | 2016-09-22 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Ornithine GC-MS (1 TMS) - 70eV, Positive | splash10-0089-9300000000-bbfdea03043e52ad8a15 | 2017-10-06 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Ornithine GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Ornithine GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Ornithine GC-MS (TMS_1_2) - 70eV, Positive | Not Available | 2021-11-05 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Ornithine GC-MS (TMS_1_3) - 70eV, Positive | Not Available | 2021-11-05 | Wishart Lab | View Spectrum |
MS/MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
---|
Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine Quattro_QQQ 10V, Positive-QTOF (Annotated) | splash10-01b9-6900000000-8fe592b77d2d8e4ae704 | 2012-07-24 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine Quattro_QQQ 25V, Positive-QTOF (Annotated) | splash10-00di-9000000000-462b84db532c33527580 | 2012-07-24 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine Quattro_QQQ 40V, Positive-QTOF (Annotated) | splash10-00di-9000000000-9c9c28d2e40d5eadacd2 | 2012-07-24 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive-QTOF | splash10-001i-0900000000-e44e06092c06bb4791af | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive-QTOF | splash10-014i-9000000000-4d6ccc429f5155b24654 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive-QTOF | splash10-014i-0900000000-dcad699e8ed7e1b19860 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive-QTOF | splash10-001i-0900000000-7b130437d4e1ceea277b | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive-QTOF | splash10-001i-0900000000-0fae230bc6b21623a4bf | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive-QTOF | splash10-014i-9000000000-5a350a8e7c607a8b9a60 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Positive-QTOF | splash10-014i-0900000000-516054b6c2f3cd4a1d02 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative-QTOF | splash10-000i-0793321000-9fef988b5ce019f84642 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative-QTOF | splash10-03di-0900000000-a612df8df5f8ba1ff7f3 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative-QTOF | splash10-001i-0910000000-97fad20414656e2b7b93 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-ITFT (LTQ Orbitrap XL, Thermo Scientfic) , Negative-QTOF | splash10-01di-0490000000-1b137b937beb110d2e4b | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-QQ (API3000, Applied Biosystems) 10V, Negative-QTOF | splash10-001i-0900000000-e3fc95eb909e45d8e648 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-QQ (API3000, Applied Biosystems) 20V, Negative-QTOF | splash10-001i-1900000000-cdd9aac89a5a71814ff3 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-QQ (API3000, Applied Biosystems) 30V, Negative-QTOF | splash10-001r-9500000000-f1cc3eccf3f5ab734222 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-QQ (API3000, Applied Biosystems) 10V, Positive-QTOF | splash10-0159-0900000000-93ce7b142d1f82f17e95 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-QQ (API3000, Applied Biosystems) 20V, Positive-QTOF | splash10-00di-9200000000-186f270471bdec40f804 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-QQ (API3000, Applied Biosystems) 30V, Positive-QTOF | splash10-00di-9000000000-ebbdf0ab6d3180cba1a5 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-QQ (API3000, Applied Biosystems) 40V, Positive-QTOF | splash10-00di-9000000000-207bcc826fb2238c2cc5 | 2012-08-31 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ornithine LC-ESI-QQ (API3000, Applied Biosystems) 50V, Positive-QTOF | splash10-00di-9000000000-a2f9a950fb23a6b18857 | 2012-08-31 | HMDB team, MONA | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Ornithine 10V, Positive-QTOF | splash10-01c9-9700000000-0364d35bb1a7c10a09c7 | 2016-09-12 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Ornithine 20V, Positive-QTOF | splash10-00dr-9100000000-9c4015733140885b4957 | 2016-09-12 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Ornithine 40V, Positive-QTOF | splash10-00dl-9000000000-b32e7180e30a835008bb | 2016-09-12 | Wishart Lab | View Spectrum |
NMR SpectraSpectrum Type | Description | Deposition Date | Source | View |
---|
Experimental 1D NMR | 1H NMR Spectrum (1D, 500 MHz, H2O, experimental) | 2012-12-04 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 100 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 100 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 200 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 200 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 300 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 300 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 400 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 400 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 500 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 500 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 600 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 600 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 700 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 700 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 800 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 800 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 900 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 900 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 1000 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 1000 MHz, D2O, predicted) | 2021-09-16 | Wishart Lab | View Spectrum | Experimental 1D NMR | 13C NMR Spectrum (1D, 400 MHz, H2O, experimental) | 2021-10-10 | Wishart Lab | View Spectrum | Experimental 2D NMR | [1H, 13C]-HSQC NMR Spectrum (2D, 600 MHz, H2O, experimental) | 2012-12-05 | Wishart Lab | View Spectrum |
IR SpectraSpectrum Type | Description | Deposition Date | Source | View |
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Predicted IR Spectrum | IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-) | 2023-02-03 | FELIX lab | View Spectrum | Predicted IR Spectrum | IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+) | 2023-02-03 | FELIX lab | View Spectrum | Predicted IR Spectrum | IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+) | 2023-02-03 | FELIX lab | View Spectrum |
|
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Disease References | Alzheimer's disease |
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- Fonteh AN, Harrington RJ, Tsai A, Liao P, Harrington MG: Free amino acid and dipeptide changes in the body fluids from Alzheimer's disease subjects. Amino Acids. 2007 Feb;32(2):213-24. Epub 2006 Oct 10. [PubMed:17031479 ]
- Tsuruoka M, Hara J, Hirayama A, Sugimoto M, Soga T, Shankle WR, Tomita M: Capillary electrophoresis-mass spectrometry-based metabolome analysis of serum and saliva from neurodegenerative dementia patients. Electrophoresis. 2013 Oct;34(19):2865-72. doi: 10.1002/elps.201300019. Epub 2013 Sep 6. [PubMed:23857558 ]
| Uremia |
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- Canepa A, Filho JC, Gutierrez A, Carrea A, Forsberg AM, Nilsson E, Verrina E, Perfumo F, Bergstrom J: Free amino acids in plasma, red blood cells, polymorphonuclear leukocytes, and muscle in normal and uraemic children. Nephrol Dial Transplant. 2002 Mar;17(3):413-21. [PubMed:11865086 ]
| Ornithine transcarbamylase deficiency |
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- Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M: Late-onset ornithine transcarbamylase deficiency in male patients: prognostic factors and characteristics of plasma amino acid profile. Pediatr Int. 2006 Apr;48(2):105-11. [PubMed:16635166 ]
| Colorectal cancer |
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- Ni Y, Xie G, Jia W: Metabonomics of human colorectal cancer: new approaches for early diagnosis and biomarker discovery. J Proteome Res. 2014 Sep 5;13(9):3857-70. doi: 10.1021/pr500443c. Epub 2014 Aug 14. [PubMed:25105552 ]
- Sinha R, Ahn J, Sampson JN, Shi J, Yu G, Xiong X, Hayes RB, Goedert JJ: Fecal Microbiota, Fecal Metabolome, and Colorectal Cancer Interrelations. PLoS One. 2016 Mar 25;11(3):e0152126. doi: 10.1371/journal.pone.0152126. eCollection 2016. [PubMed:27015276 ]
- Goedert JJ, Sampson JN, Moore SC, Xiao Q, Xiong X, Hayes RB, Ahn J, Shi J, Sinha R: Fecal metabolomics: assay performance and association with colorectal cancer. Carcinogenesis. 2014 Sep;35(9):2089-96. doi: 10.1093/carcin/bgu131. Epub 2014 Jul 18. [PubMed:25037050 ]
| Schizophrenia |
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- He Y, Yu Z, Giegling I, Xie L, Hartmann AM, Prehn C, Adamski J, Kahn R, Li Y, Illig T, Wang-Sattler R, Rujescu D: Schizophrenia shows a unique metabolomics signature in plasma. Transl Psychiatry. 2012 Aug 14;2:e149. doi: 10.1038/tp.2012.76. [PubMed:22892715 ]
| Early preeclampsia |
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- Bahado-Singh RO, Akolekar R, Mandal R, Dong E, Xia J, Kruger M, Wishart DS, Nicolaides K: Metabolomics and first-trimester prediction of early-onset preeclampsia. J Matern Fetal Neonatal Med. 2012 Oct;25(10):1840-7. doi: 10.3109/14767058.2012.680254. Epub 2012 Apr 28. [PubMed:22494326 ]
| Pregnancy |
---|
- Bahado-Singh RO, Akolekar R, Mandal R, Dong E, Xia J, Kruger M, Wishart DS, Nicolaides K: Metabolomics and first-trimester prediction of early-onset preeclampsia. J Matern Fetal Neonatal Med. 2012 Oct;25(10):1840-7. doi: 10.3109/14767058.2012.680254. Epub 2012 Apr 28. [PubMed:22494326 ]
- Bahado-Singh RO, Akolekar R, Mandal R, Dong E, Xia J, Kruger M, Wishart DS, Nicolaides K: First-trimester metabolomic detection of late-onset preeclampsia. Am J Obstet Gynecol. 2013 Jan;208(1):58.e1-7. doi: 10.1016/j.ajog.2012.11.003. Epub 2012 Nov 13. [PubMed:23159745 ]
- Bahado-Singh RO, Akolekar R, Mandal R, Dong E, Xia J, Kruger M, Wishart DS, Nicolaides K: Metabolomic analysis for first-trimester Down syndrome prediction. Am J Obstet Gynecol. 2013 May;208(5):371.e1-8. doi: 10.1016/j.ajog.2012.12.035. Epub 2013 Jan 8. [PubMed:23313728 ]
- Bahado-Singh RO, Akolekar R, Chelliah A, Mandal R, Dong E, Kruger M, Wishart DS, Nicolaides K: Metabolomic analysis for first-trimester trisomy 18 detection. Am J Obstet Gynecol. 2013 Jul;209(1):65.e1-9. doi: 10.1016/j.ajog.2013.03.028. Epub 2013 Mar 25. [PubMed:23535240 ]
- Bahado-Singh RO, Ertl R, Mandal R, Bjorndahl TC, Syngelaki A, Han B, Dong E, Liu PB, Alpay-Savasan Z, Wishart DS, Nicolaides KH: Metabolomic prediction of fetal congenital heart defect in the first trimester. Am J Obstet Gynecol. 2014 Sep;211(3):240.e1-240.e14. doi: 10.1016/j.ajog.2014.03.056. Epub 2014 Apr 1. [PubMed:24704061 ]
| Late-onset preeclampsia |
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| Lysinuric protein intolerance |
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- Kurko J, Tringham M, Tanner L, Nanto-Salonen K, Vaha-Makila M, Nygren H, Poho P, Lietzen N, Mattila I, Olkku A, Hyotylainen T, Oresic M, Simell O, Niinikoski H, Mykkanen J: Imbalance of plasma amino acids, metabolites and lipids in patients with lysinuric protein intolerance (LPI). Metabolism. 2016 Sep;65(9):1361-75. doi: 10.1016/j.metabol.2016.05.012. Epub 2016 May 27. [PubMed:27506743 ]
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| Fumarase deficiency |
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- Allegri G, Fernandes MJ, Scalco FB, Correia P, Simoni RE, Llerena JC Jr, de Oliveira ML: Fumaric aciduria: an overview and the first Brazilian case report. J Inherit Metab Dis. 2010 Aug;33(4):411-9. doi: 10.1007/s10545-010-9134-2. Epub 2010 Jun 15. [PubMed:20549362 ]
| N-acetylglutamate synthetase deficiency |
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- Guffon N, Vianey-Saban C, Bourgeois J, Rabier D, Colombo JP, Guibaud P: A new neonatal case of N-acetylglutamate synthase deficiency treated by carbamylglutamate. J Inherit Metab Dis. 1995;18(1):61-5. [PubMed:7623444 ]
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| Obesity |
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- Simone Wahl, Christina Holzapfel, Zhonghao Yu, Michaela Breier, Ivan Kondofersky, Christiane Fuchs, Paula Singmann, Cornelia Prehn, Jerzy Adamski, Harald Grallert, Thomas Illig, Rui Wang-Sattler, Thomas Reinehr (2013). Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children. Metabolomics.
| Pearson Syndrome |
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- Crippa BL, Leon E, Calhoun A, Lowichik A, Pasquali M, Longo N: Biochemical abnormalities in Pearson syndrome. Am J Med Genet A. 2015 Mar;167A(3):621-8. doi: 10.1002/ajmg.a.36939. [PubMed:25691415 ]
| Hyperornithinemia with Gyrate Atrophy |
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- Simell O, Takki K: Raised plasma-ornithine and gyrate atrophy of the choroid and retina. Lancet. 1973 May 12;1(7811):1031-3. [PubMed:4122112 ]
| Cutis laxa, autosomal recessive, type IIIA |
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- Baumgartner MR, Hu CA, Almashanu S, Steel G, Obie C, Aral B, Rabier D, Kamoun P, Saudubray JM, Valle D: Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding delta(1)-pyrroline-5-carboxylate synthase. Hum Mol Genet. 2000 Nov 22;9(19):2853-8. [PubMed:11092761 ]
| Myopathy, lactic acidosis, and sideroblastic anemia 1 |
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- Parfait B, de Lonlay P, von Kleist-Retzow JC, Cormier-Daire V, Chretien D, Rotig A, Rabier D, Saudubray JM, Rustin P, Munnich A: The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia. Eur J Pediatr. 1999 Jan;158(1):55-8. [PubMed:9950309 ]
| Leukemia |
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- Peng CT, Wu KH, Lan SJ, Tsai JJ, Tsai FJ, Tsai CH: Amino acid concentrations in cerebrospinal fluid in children with acute lymphoblastic leukemia undergoing chemotherapy. Eur J Cancer. 2005 May;41(8):1158-63. Epub 2005 Apr 14. [PubMed:15911239 ]
| Autism |
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- De Angelis M, Piccolo M, Vannini L, Siragusa S, De Giacomo A, Serrazzanetti DI, Cristofori F, Guerzoni ME, Gobbetti M, Francavilla R: Fecal microbiota and metabolome of children with autism and pervasive developmental disorder not otherwise specified. PLoS One. 2013 Oct 9;8(10):e76993. doi: 10.1371/journal.pone.0076993. eCollection 2013. [PubMed:24130822 ]
| Crohn's disease |
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- Kolho KL, Pessia A, Jaakkola T, de Vos WM, Velagapudi V: Faecal and Serum Metabolomics in Paediatric Inflammatory Bowel Disease. J Crohns Colitis. 2017 Mar 1;11(3):321-334. doi: 10.1093/ecco-jcc/jjw158. [PubMed:27609529 ]
| Ulcerative colitis |
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- Kolho KL, Pessia A, Jaakkola T, de Vos WM, Velagapudi V: Faecal and Serum Metabolomics in Paediatric Inflammatory Bowel Disease. J Crohns Colitis. 2017 Mar 1;11(3):321-334. doi: 10.1093/ecco-jcc/jjw158. [PubMed:27609529 ]
| Perillyl alcohol administration for cancer treatment |
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- Sugimoto M, Wong DT, Hirayama A, Soga T, Tomita M: Capillary electrophoresis mass spectrometry-based saliva metabolomics identified oral, breast and pancreatic cancer-specific profiles. Metabolomics. 2010 Mar;6(1):78-95. Epub 2009 Sep 10. [PubMed:20300169 ]
| Pancreatic cancer |
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- Sugimoto M, Wong DT, Hirayama A, Soga T, Tomita M: Capillary electrophoresis mass spectrometry-based saliva metabolomics identified oral, breast and pancreatic cancer-specific profiles. Metabolomics. 2010 Mar;6(1):78-95. Epub 2009 Sep 10. [PubMed:20300169 ]
| Periodontal disease |
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- Sugimoto M, Wong DT, Hirayama A, Soga T, Tomita M: Capillary electrophoresis mass spectrometry-based saliva metabolomics identified oral, breast and pancreatic cancer-specific profiles. Metabolomics. 2010 Mar;6(1):78-95. Epub 2009 Sep 10. [PubMed:20300169 ]
| Frontotemporal dementia |
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- Tsuruoka M, Hara J, Hirayama A, Sugimoto M, Soga T, Shankle WR, Tomita M: Capillary electrophoresis-mass spectrometry-based metabolome analysis of serum and saliva from neurodegenerative dementia patients. Electrophoresis. 2013 Oct;34(19):2865-72. doi: 10.1002/elps.201300019. Epub 2013 Sep 6. [PubMed:23857558 ]
| Lewy body disease |
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- Tsuruoka M, Hara J, Hirayama A, Sugimoto M, Soga T, Shankle WR, Tomita M: Capillary electrophoresis-mass spectrometry-based metabolome analysis of serum and saliva from neurodegenerative dementia patients. Electrophoresis. 2013 Oct;34(19):2865-72. doi: 10.1002/elps.201300019. Epub 2013 Sep 6. [PubMed:23857558 ]
| Cystinuria |
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- Fjellstedt E, Harnevik L, Jeppsson JO, Tiselius HG, Soderkvist P, Denneberg T: Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds. Urol Res. 2003 Dec;31(6):417-25. Epub 2003 Oct 25. [PubMed:14586528 ]
- G.Frauendienst-Egger, Friedrich K. Trefz (2017). MetaGene: Metabolic & Genetic Information Center (MIC: http://www.metagene.de). METAGENE consortium.
| Eosinophilic esophagitis |
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- Slae, M., Huynh, H., Wishart, D.S. (2014). Analysis of 30 normal pediatric urine samples via NMR spectroscopy (unpublished work). NA.
| Hyperdibasic aminoaciduria I |
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- Whelan DT, Scriver CR: Hyperdibasicaminoaciduria: an inherited disorder of amino acid transport. Pediatr Res. 1968 Nov;2(6):525-34. [PubMed:5727921 ]
| Hyperlysinemia I, familial |
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- Tondo M, Calpena E, Arriola G, Sanz P, Martorell L, Ormazabal A, Castejon E, Palacin M, Ugarte M, Espinos C, Perez B, Perez-Duenas B, Perez-Cerda C, Artuch R: Clinical, biochemical, molecular and therapeutic aspects of 2 new cases of 2-aminoadipic semialdehyde synthase deficiency. Mol Genet Metab. 2013 Nov;110(3):231-6. doi: 10.1016/j.ymgme.2013.06.021. Epub 2013 Jul 6. [PubMed:23890588 ]
| Hyperlysinuria |
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- Fjellstedt E, Harnevik L, Jeppsson JO, Tiselius HG, Soderkvist P, Denneberg T: Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds. Urol Res. 2003 Dec;31(6):417-25. Epub 2003 Oct 25. [PubMed:14586528 ]
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