Record Information |
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Version | 2.0 |
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Created at | 2005-11-16 15:48:42 UTC |
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Updated at | 2021-08-10 02:54:40 UTC |
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NP-MRD ID | NP0000642 |
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Secondary Accession Numbers | None |
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Natural Product Identification |
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Common Name | Indolelactic acid |
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Description | Indolelactic acid is a tryptophan metabolite found in human plasma and serum and normal urine. Tryptophan is metabolized by two major pathways in humans, either through kynurenine or via a series of indoles, and some of its metabolites are known to be biologically active. Indolelactic acid is present in various amounts, significantly higher in umbilical foetal plasma than in maternal plasma in the protein-bound form. (PMID 2361979 , 1400722 , 3597614 , 11060358 , 1400722 ). |
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Structure | [H]OC(=O)[C@]([H])(O[H])C([H])([H])C1=C([H])N([H])C2=C([H])C([H])=C([H])C([H])=C12 InChI=1S/C11H11NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,10,12-13H,5H2,(H,14,15)/t10-/m1/s1 |
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Synonyms | Value | Source |
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Indolelactate | Generator | 3-(indol-3-yl) LACTic acid | HMDB | (2S)-2-Hydroxy-3-(1H-indol-3-yl)propanoic acid | HMDB | (2S)-2-Hydroxy-3-(1H-indol-3-yl)propionic acid | HMDB | (2S)-2-Hydroxy-3-indoylpropanoic acid | HMDB | (2S)-2-Hydroxy-3-indoylpropionic acid | HMDB | (S)-2-Hydroxy-3-(1H-indol-3-yl)propanoic acid | HMDB | (S)-2-Hydroxy-3-(1H-indol-3-yl)propionic acid | HMDB | (S)-Indole-3-lactic acid | HMDB | (AlphaS)-alpha-hydroxy-1H-indole-3-propanoic acid | HMDB | (AlphaS)-alpha-hydroxy-1H-indole-3-propionic acid | HMDB | (ΑS)-α-hydroxy-1H-indole-3-propanoic acid | HMDB | (ΑS)-α-hydroxy-1H-indole-3-propionic acid | HMDB | 2-(1H-indol-3-yl)Acetaldehyde | HMDB | 2-Hydroxy-3-(1H-indol-3-yl)propanoic acid | HMDB | 2-Hydroxy-3-(1H-indol-3-yl)propionic acid | HMDB | 2-Hydroxy-3-(3-indolyl)propanoic acid | HMDB | 2-Hydroxy-3-(3-indolyl)propionic acid | HMDB | 3-(3-Indolyl)-2-hydroxypropanoic acid | HMDB | 3-(3-Indolyl)-2-hydroxypropionic acid | HMDB | 3-(3-Indolyl)-DL-lactic acid | HMDB | 3-Indolyllactic acid | HMDB | Indole-3-L-lactic acid | HMDB | Indole-3-lactic acid | HMDB | L-3-(3-Indolyl)lactic acid | HMDB | L-Indole-3-lactic acid | HMDB | alpha-Hydroxy-1H-indole-3-propanoic acid | HMDB | alpha-Hydroxy-1H-indole-3-propionic acid | HMDB | beta-(3-Indolyl)lactic acid | HMDB | beta-Indolyllactic acid | HMDB | Α-hydroxy-1H-indole-3-propanoic acid | HMDB | Α-hydroxy-1H-indole-3-propionic acid | HMDB | Β-(3-indolyl)lactic acid | HMDB | Β-indolyllactic acid | HMDB | Indolelactic acid | HMDB |
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Chemical Formula | C11H11NO3 |
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Average Mass | 205.2099 Da |
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Monoisotopic Mass | 205.07389 Da |
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IUPAC Name | (2R)-2-hydroxy-3-(1H-indol-3-yl)propanoic acid |
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Traditional Name | (R)-indole-3-lactic acid |
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CAS Registry Number | 1821-52-9 |
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SMILES | [H]OC(=O)[C@]([H])(O[H])C([H])([H])C1=C([H])N([H])C2=C([H])C([H])=C([H])C([H])=C12 |
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InChI Identifier | InChI=1S/C11H11NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,10,12-13H,5H2,(H,14,15)/t10-/m1/s1 |
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InChI Key | XGILAAMKEQUXLS-JTQLQIEISA-N |
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Experimental Spectra |
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| Spectrum Type | Description | Depositor Email | Depositor Organization | Depositor | Deposition Date | View |
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1D NMR | 1H NMR Spectrum (1D, 500 MHz, H2O, experimental) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 500 MHz, D2O, simulated) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 500 MHz, D2O, simulated) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 500 MHz, D2O, experimental) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 2D NMR | [1H, 13C]-HSQC NMR Spectrum (2D, 600 MHz, H2O, experimental) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum |
| Predicted Spectra |
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| Spectrum Type | Description | Depositor ID | Depositor Organization | Depositor | Deposition Date | View |
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1D NMR | 13C NMR Spectrum (1D, 25 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 100 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 252 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 1000 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 50 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 200 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 75 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 300 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 101 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 400 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 126 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 500 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 151 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 600 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 176 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 700 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 201 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 800 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 226 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 900 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum |
| Chemical Shift Submissions |
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| Not Available | Species |
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Species of Origin | |
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Species Where Detected | |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. Indolyl carboxylic acids and derivatives are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring. |
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Kingdom | Organic compounds |
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Super Class | Organoheterocyclic compounds |
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Class | Indoles and derivatives |
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Sub Class | Indolyl carboxylic acids and derivatives |
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Direct Parent | Indolyl carboxylic acids and derivatives |
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Alternative Parents | |
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Substituents | - Indolyl carboxylic acid derivative
- 3-alkylindole
- Indole
- Alpha-hydroxy acid
- Hydroxy acid
- Substituted pyrrole
- Benzenoid
- Pyrrole
- Heteroaromatic compound
- Secondary alcohol
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Carboxylic acid derivative
- Azacycle
- Hydrocarbon derivative
- Alcohol
- Organooxygen compound
- Organonitrogen compound
- Organic oxide
- Organopnictogen compound
- Organic oxygen compound
- Carbonyl group
- Organic nitrogen compound
- Aromatic heteropolycyclic compound
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Molecular Framework | Aromatic heteropolycyclic compounds |
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External Descriptors | Not Available |
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Physical Properties |
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State | Solid |
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Experimental Properties | Property | Value | Reference |
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Melting Point | Not Available | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | 17 mg/mL | Not Available | LogP | Not Available | Not Available |
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Predicted Properties | |
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