| In ZINC since | Heavy atoms | Benign functionality |
|---|---|---|
| July 28th, 2004 | 13 | No |
Popular Name: 5-Hydroxyindoleacetaldehyde 5-Hydroxyindoleacetaldehyde
Find On: PubMed — Wikipedia — Google
CAS Number: 1892-21-3
(5-hydroxyindol-3-yl)acetaldehyde
2-(5-hydroxy-1H-indol-3-yl)acetaldehyde
5-Hydroxyindoleacetaldehyde; C05634
| Type pH range | xlogP | Des A‑Pol Apolar desolvation (kcal/mol) | Des Pol Polar desolvation (kcal/mol) | H Don H-bond donors | H Acc H-bond acceptors | Chg Net charge | tPSA (Ų) | MWT Molecular weight (g/mol) | RB Rotatable bonds | DL |
|---|---|---|---|---|---|---|---|---|---|---|
| Ref Reference (pH 7) | 1.58 | -1.28 | -8.63 | 2 | 3 | 0 | 53 | 175.187 | 2 | ↓ |
| Note Type | Comments | Provided By |
|---|---|---|
| Patent Database Links | EP1645272; US2007270332 | ChEBI |
| Reactome Database Links | REACT_15407; REACT_1795 | ChEBI |
| PUBCHEM_PATENT_ID | WO1994011397A1 | IBM Patent Data |
| Description | Species |
|---|---|
| Metabolism of serotonin |
|
| Monoamines are oxidized to aldehydes by MAOA and MAOB, producing NH3 and H2O2 |
