| Identification | Back Directory | [Name]
5-HYDROXYTRYPTOPHOL | [CAS]
154-02-9 | [Synonyms]
NSC 84416
hydroxytryptophol
3-(2-Hydroxyethyl)
5-HYDROXYTRYPTOPHOL
5-HYDROXYINDOLE-3-ETHANOL
5-hydroxy-indole-3-ethano
5-HYDROXYTRYPTOPHOL(5OHIEt)
5-hydroxy-1h-indole-3-ethano
5-hydroxy-1h-indole-3-ethanol
5-hydroxytryptophol crystalline
3-(2-hydroxyethyl)-1H-indol-5-ol
5-Hydroxy-3-(2-hydroxyethyl)indole
2-(5-HYDROXY-3-INDOLYL)ETHYL ALCOHOL
5-Hydroxy-3-(2-hydroxyethyl)-1H-indole
DL-2-amino-3-(5-fluoro-3-indolyl)propionic acid | [EINECS(EC#)]
205-820-4 | [Molecular Formula]
C10H11NO2 | [MDL Number]
MFCD00047197 | [MOL File]
154-02-9.mol | [Molecular Weight]
177.2 |
| Chemical Properties | Back Directory | [Appearance]
Off-White Crystalline Powder | [Melting point ]
111-113°? | [Boiling point ]
435.2±30.0 °C(Predicted) | [density ]
1.356±0.06 g/cm3(Predicted) | [storage temp. ]
−20°C | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
10.07±0.40(Predicted) | [color ]
White to Light Red |
| Hazard Information | Back Directory | [Chemical Properties]
Off-White Crystalline Powder | [Uses]
A metabolite of Tryptophan (T947200). | [Hazard]
A reproductive hazard. | [Definition]
ChEBI: 5-Hydroxytryptophol is a member of indoles. | [Biological Activity]
5-hydroxy tryptophol is a metabolite of tryptophan.tryptophan (encoded by the codon ugg) is an α-amino acid that is used in the biosynthesis of proteins. tryptophan has an α-amino group, an α-carboxylic acid group, and a side chain indole, demonstrating it as a non-polar, aromatic amino acid. tryptophan is critical in humans, but the body cannot synthesize it and therefore tryptophan must be obtained from the diet. tryptophan is also found to be a precursor to the neurotransmitters serotonin and melatonin. | [Synthesis]
General procedure for the synthesis of 5-hydroxychromanol from 5-hydroxyindole-3-acetic acid:
1. 3-(2-hydroxyethyl)-1H-indole (F-3, 1.99 g, 52.3 mmol) and LiAlH4 (1.99 g, 52.3 mmol) were placed in a reaction flask under argon protection.
2. Anhydrous THF (60 ml) was added to dissolve 5-hydroxy-1H-indole-3-acetic acid (5.00 g, 26.2 mmol) and THF (100 ml) was added dropwise over 30 min.
3. The reaction mixture was heated to reflux for 3 hours.
4. After completion of the reaction, the reaction was cooled in an ice bath and THF (10 ml) and H2O (4 ml) were added slowly and stirred for 30 min.
5. The reaction mixture was filtered through diatomaceous earth and the filter cake was washed with dichloromethane (150 ml).
6. The filtrate was concentrated under reduced pressure to give the crude product.
7. Yield: 2.17 g (47%). 8.
8. Product characterization: 1H-NMR (DMSO-d6): δ 2.74 (2H, m); 3.60 (3H, m); 6.58 (1H, m); 6.78 (1H, s); 6.99 (1H, s); 7.08 (1H, d); 10.5 (1H, bs). | [in vitro]
in previous studies, 5-hydroxy tryptophol was identified as a metabolite of tryptophan that was formed by the alcohol dehydrogenase-catalyzed reduction of the serotonin intermediate, 5-hydroxyindoleacetaldehyde. moreover, depending on the tissue nad/nadh ratio, the acetaldehyde intermediate could also be oxidized by aldehyde dehydrogenase to form 5-hydroxyindoleacetic acid. therefore, the ratio of 5-hydroxy tryptophol to 5-hydroxyindoleacetic acid could be used as a biomarker for recent alcohol consumption [1,2]. | [storage]
Store at -20°C | [References]
[1] yokoyama, m. t. and carlson, j.r. dissimilation of tryptophan and related indolic compounds by ruminal microorganisms in vitro. appl.microbiol. 27(3), 540-548 (1974).
[2] beck, o. ,stephanson, n.,btthcer, m., et al. biomarkers to disclose recent intake of alcohol: potential of 5-hydroxytryptophol glucuronide testing using new direct uplc-tandem ms and elisa methods. alcohol & alcoholism 42(4), 321-325 (2007). |
|
| Company Name: |
Cool Pharm, Ltd
|
| Tel: |
021-60455363 18019463053 |
| Website: |
www.coolpharm.com |
|