| Record Information |
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| Version | 2.0 |
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| Created at | 2022-02-14 20:49:23 UTC |
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| Updated at | 2022-03-10 22:21:52 UTC |
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| NP-MRD ID | NP0044366 |
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| Secondary Accession Numbers | None |
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| Natural Product Identification |
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| Common Name | NADHX |
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| Description | NADHX, also known as (6S)-6-beta-hydroxy-1,4,5,6-tetrahydronicotinamide-adenine dinucleotide, (S)-nadh-hydrate or (S)-nadhx, belongs to the class of organic compounds known as purine nucleotide sugars. These are purine nucleotides bound to a saccharide derivative through the terminal phosphate group. A tetrahydronicotinamide adenine dinucleotide obtained by formal stereo- and regioselective hydration across the 5,6-double bond in the nicotinyl ring of NADH, with the hydroxy group located at position 6, having (S)-configuration. NADHX is a very strong basic compound (based on its pKa). It exists in all living organisms, ranging from bacteria to humans. Outside of the human body, NADHX has been detected, but not quantified in, several different foods, such as pineapples, fireweeds, silver lindens, mentha (mint), and broad beans. This could make NADHX a potential biomarker for the consumption of these foods. NADHX is expected to be in Cannabis as all living plants are known to produce and metabolize it. |
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| Structure | [H][C@]1(COP(O)(=O)OP(O)(=O)OC[C@@]2([H])O[C@@]([H])(N3C=C(CC[C@]3([H])O)C(O)=N)[C@]([H])(O)[C@]2([H])O)O[C@@]([H])(N2C=NC3=C(N)N=CN=C23)[C@]([H])(O)[C@]1([H])O InChI=1S/C21H31N7O15P2/c22-17-12-19(25-6-24-17)28(7-26-12)21-16(33)14(31)10(42-21)5-40-45(37,38)43-44(35,36)39-4-9-13(30)15(32)20(41-9)27-3-8(18(23)34)1-2-11(27)29/h3,6-7,9-11,13-16,20-21,29-33H,1-2,4-5H2,(H2,23,34)(H,35,36)(H,37,38)(H2,22,24,25)/t9-,10-,11+,13-,14-,15-,16-,20-,21-/m1/s1 |
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| Synonyms | | Value | Source |
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| (6S)-6beta-Hydroxy-1,4,5,6-tetrahydronicotinamide adenine dinucleotide | ChEBI | | 6beta-Hydroxy-1,4,5,6-tetrahydronicotinamide-adenine dinucleotide | ChEBI | | BETA-6-HYDROXY-1,4,5,6-tetrhydronicotinamide adenine dinucleotide | ChEBI | | (6S)-6b-Hydroxy-1,4,5,6-tetrahydronicotinamide adenine dinucleotide | Generator | | (6S)-6β-hydroxy-1,4,5,6-tetrahydronicotinamide adenine dinucleotide | Generator | | 6b-Hydroxy-1,4,5,6-tetrahydronicotinamide-adenine dinucleotide | Generator | | 6β-hydroxy-1,4,5,6-tetrahydronicotinamide-adenine dinucleotide | Generator | | b-6-HYDROXY-1,4,5,6-tetrhydronicotinamide adenine dinucleotide | Generator | | β-6-hydroxy-1,4,5,6-tetrhydronicotinamide adenine dinucleotide | Generator | | (S)-NADH-hydrate | KEGG | | (S)-NADHX | KEGG | | (6S)-6-Hydroxy-1,4,5,6-tetrahydronicotinamide-adenine dinucleotide | KEGG | | (S)-NADH-hydric acid | Generator | | (6S)-6b-Hydroxy-1,4,5,6-tetrahydronicotinamide-adenine dinucleotide | Generator | | (6S)-6Β-hydroxy-1,4,5,6-tetrahydronicotinamide-adenine dinucleotide | Generator | | (6S)-6-b-Hydroxy-1,4,5,6-tetrahydronicotinamide-adenine dinucleotide | Generator | | (6S)-6-Β-hydroxy-1,4,5,6-tetrahydronicotinamide-adenine dinucleotide | Generator | | Monohydroxytetrahydronicotinamide adenine dinucleotide | HMDB | | NADHX | HMDB |
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| Chemical Formula | C21H31N7O15P2 |
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| Average Mass | 683.4563 Da |
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| Monoisotopic Mass | 683.13534 Da |
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| IUPAC Name | [({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]({[(2R,3S,4R,5R)-5-[(2S)-5-carbamoyl-2-hydroxy-1,2,3,4-tetrahydropyridin-1-yl]-3,4-dihydroxyoxolan-2-yl]methoxy})phosphinic acid |
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| Traditional Name | (S)-nadhx |
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| CAS Registry Number | 116561-22-9 |
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| SMILES | [H][C@]1(COP(O)(=O)OP(O)(=O)OC[C@@]2([H])O[C@@]([H])(N3C=C(CC[C@]3([H])O)C(O)=N)[C@]([H])(O)[C@]2([H])O)O[C@@]([H])(N2C=NC3=C(N)N=CN=C23)[C@]([H])(O)[C@]1([H])O |
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| InChI Identifier | InChI=1S/C21H31N7O15P2/c22-17-12-19(25-6-24-17)28(7-26-12)21-16(33)14(31)10(42-21)5-40-45(37,38)43-44(35,36)39-4-9-13(30)15(32)20(41-9)27-3-8(18(23)34)1-2-11(27)29/h3,6-7,9-11,13-16,20-21,29-33H,1-2,4-5H2,(H2,23,34)(H,35,36)(H,37,38)(H2,22,24,25)/t9-,10-,11+,13-,14-,15-,16-,20-,21-/m1/s1 |
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| InChI Key | IDBZKGQRLBFUFQ-VPHRTNKSSA-N |
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| Experimental Spectra |
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| Not Available | | 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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| Chemical Taxonomy |
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| Description | Belongs to the class of organic compounds known as purine nucleotide sugars. These are purine nucleotides bound to a saccharide derivative through the terminal phosphate group. |
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| Kingdom | Organic compounds |
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| Super Class | Nucleosides, nucleotides, and analogues |
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| Class | Purine nucleotides |
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| Sub Class | Purine nucleotide sugars |
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| Direct Parent | Purine nucleotide sugars |
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| Alternative Parents | |
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| Substituents | - Purine nucleotide sugar
- Purine ribonucleoside diphosphate
- Purine ribonucleoside monophosphate
- Nicotinamide-nucleotide
- Pentose phosphate
- Pentose-5-phosphate
- Glycosyl compound
- N-glycosyl compound
- 6-aminopurine
- Monosaccharide phosphate
- Organic pyrophosphate
- Imidazopyrimidine
- Purine
- Aminopyrimidine
- Monoalkyl phosphate
- Tetrahydropyridine
- Imidolactam
- Alkyl phosphate
- Hydropyridine
- Pyrimidine
- Monosaccharide
- N-substituted imidazole
- Organic phosphoric acid derivative
- Phosphoric acid ester
- Azole
- Vinylogous amide
- Tetrahydrofuran
- Imidazole
- Heteroaromatic compound
- Primary carboxylic acid amide
- Carboxamide group
- Secondary alcohol
- Amino acid or derivatives
- Organoheterocyclic compound
- Oxacycle
- Carboxylic acid derivative
- Azacycle
- Alkanolamine
- Organonitrogen compound
- Organooxygen compound
- Organic nitrogen compound
- Carbonyl group
- Organic oxygen compound
- Organopnictogen compound
- Alcohol
- Primary amine
- Amine
- Organic oxide
- Hydrocarbon derivative
- Aromatic heteropolycyclic compound
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| Molecular Framework | Aromatic heteropolycyclic compounds |
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| External Descriptors | |
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| Physical Properties |
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| State | Not Available |
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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 | Not Available | Not Available | | LogP | Not Available | Not Available |
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| Predicted Properties | |
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