IMPPAT Phytochemical information: 
Toddaquinoline

Toddaquinoline
Summary

SMILES: Oc1cnc2c(c1)ccc1c2cc2OCOc2c1
InChI: InChI=1S/C14H9NO3/c16-10-3-9-2-1-8-4-12-13(18-7-17-12)5-11(8)14(9)15-6-10/h1-6,16H,7H2
InChIKey: NKZCRLAOZWABNB-UHFFFAOYSA-N
DeepSMILES: Occnccc6)cccc6ccOCOc5c9
Scaffold Graph/Node/Bond level: c1cnc2c(c1)ccc1cc3c(cc12)OCO3
Scaffold Graph/Node level: C1CNC2C(C1)CCC1CC3OCOC3CC12
Scaffold Graph level: C1CC2CC3CCC4CCCCC4C3CC2C1
Functional groups: cO; cnc; c1cOCO1
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organoheterocyclic compounds
ClassyFire Class: Quinolines and derivatives
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Tryptophan alkaloids|Anthranilic acid alkaloids
NP Classifier Class: Quinoline alkaloids
Synonymous chemical names:
toddaquinoline, Toddaquinoline
External chemical identifiers:
CID:CID_11390791; ChEMBL:CHEMBL470880
Chemical structure download


Toddaquinoline
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 239.23
Log P RDKit 2.82
Topological polar surface area (Å2) RDKit 51.58
Number of hydrogen bond acceptors RDKit 4
Number of hydrogen bond donors RDKit 1
Number of carbon atoms RDKit 14
Number of heavy atoms RDKit 18
Number of heteroatoms RDKit 4
Number of nitrogen atoms RDKit 1
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 13
Number of sp3 hybridized carbon atoms RDKit 1
Shape complexity RDKit 0.07
Number of rotatable bonds RDKit 0
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 1
Number of aliphatic rings RDKit 1
Number of aromatic carbocycles RDKit 2
Number of aromatic heterocycles RDKit 1
Number of aromatic rings RDKit 3
Total number of rings RDKit 4
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 4


Toddaquinoline
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 0
Lipinski’s rule of 5 RDKit Passed
Number of Ghose rule violations RDKit 0
Ghose rule RDKit Passed
Veber rule RDKit Good
Egan rule RDKit Good
GSK 4/400 rule RDKit Good
Pfizer 3/75 rule RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.61


Toddaquinoline
ADME 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 -5.70
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 1
CYP1A2 inhibitor SwissADME Yes
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME No
CYP2D6 inhibitor SwissADME Yes
CYP3A4 inhibitor SwissADME Yes
P-glycoprotein substrate SwissADME Yes