IMPPAT Phytochemical information: 
N,N-Dimethyl-5-methoxytryptamine
N,N-Dimethyl-5-methoxytryptamine
Summary

SMILES: COc1ccc2c(c1)c(CCN(C)C)c[nH]2
InChI: InChI=1S/C13H18N2O/c1-15(2)7-6-10-9-14-13-5-4-11(16-3)8-12(10)13/h4-5,8-9,14H,6-7H2,1-3H3
InChIKey: ZSTKHSQDNIGFLM-UHFFFAOYSA-N
DeepSMILES: COcccccc6)cCCNC)C))))c[nH]5
Scaffold Graph/Node/Bond level: c1ccc2[nH]ccc2c1
Scaffold Graph/Node level: C1CCC2NCCC2C1
Scaffold Graph level: C1CCC2CCCC2C1
Functional groups: CN(C)C; cOC; c[nH]c
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organoheterocyclic compounds
ClassyFire Class: Indoles and derivatives
ClassyFire Subclass: Tryptamines and derivatives
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Tryptophan alkaloids
NP Classifier Class: Simple indole alkaloids
Synonymous chemical names:
5-methoxy-n,n-dimethyltryptamin, 5-methoxy-n,n-dimethyltryptamine, n,n-dimethyl-5-methoxytryptamine
External chemical identifiers:
CID:1832; ChEMBL:CHEMBL7257; ChEBI:2086; ZINC:ZINC000000057152; FDASRS:X0MKX3GWU9; SureChEMBL:SCHEMBL132733
Chemical structure download
2D:2D MOL2D MOL22D SDF
3D:3D MOL3D MOL23D SDF3D PDB3D PDBQT
N,N-Dimethyl-5-methoxytryptamine
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 218.3
Log P RDKit 2.28
Topological polar surface area (Å2) RDKit 28.26
Number of hydrogen bond acceptors RDKit 2
Number of hydrogen bond donors RDKit 1
Number of carbon atoms RDKit 13
Number of heavy atoms RDKit 16
Number of heteroatoms RDKit 3
Number of nitrogen atoms RDKit 2
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 0
Stereochemical complexity RDKit 0
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 8
Number of sp3 hybridized carbon atoms RDKit 5
Shape complexity RDKit 0.38
Number of rotatable bonds RDKit 4
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 0
Number of aliphatic rings RDKit 0
Number of aromatic carbocycles RDKit 1
Number of aromatic heterocycles RDKit 1
Number of aromatic rings RDKit 2
Total number of rings RDKit 2
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 0
Number of saturated rings RDKit 0
Number of Smallest Set of Smallest Rings (SSSR) RDKit 2
N,N-Dimethyl-5-methoxytryptamine
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 0
Lipinski’s rule of 5 filter RDKit Passed
Number of Ghose filter violations RDKit 0
Ghose filter RDKit Passed
Veber filter RDKit Good
Pfizer 3/75 filter RDKit Bad
GSK 4/400 filter RDKit Good
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.8524
N,N-Dimethyl-5-methoxytryptamine
ADMET properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Soluble
Solubility class [Silicos-IT] SwissADME Moderately soluble
Blood Brain Barrier permeation SwissADME Yes
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -5.65
Number of PAINS structural alerts SwissADME 0.0
Number of Brenk structural alerts SwissADME 0.0
CYP1A2 inhibitor SwissADME Yes
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME No
CYP2D6 inhibitor SwissADME Yes
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME No
N,N-Dimethyl-5-methoxytryptamine
Predicted human target proteins
Protein identifierHGNC symbolCombined score from STITCH database
ENSP00000276198HTR2C961
ENSP00000289753HTR6823
ENSP00000307766HTR1E914
ENSP00000313661HTR1D779
ENSP00000316244HTR1A926
ENSP00000322924HTR1F940
ENSP00000337949HTR7862
ENSP00000358963HTR1B790
ENSP00000367959HTR2A923
The human target proteins were predicted using STITCH, a database of Chemical-Protein interaction networks.