IMPPAT Phytochemical information: 
Hippeastrine N-oxide

Hippeastrine N-oxide
Summary

SMILES: O[C@H]1C=C2CC[N+]([C@H]2[C@H]2[C@@H]1OC(=O)c1c2cc2c(c1)OCO2)([O-])C
InChI: InChI=1S/C17H17NO6/c1-18(21)3-2-8-4-11(19)16-14(15(8)18)9-5-12-13(23-7-22-12)6-10(9)17(20)24-16/h4-6,11,14-16,19H,2-3,7H2,1H3/t11-,14-,15+,16+,18?/m0/s1
InChIKey: MSPKPJXNNSETAB-QEJHCFMCSA-N
DeepSMILES: O[C@H]C=CCC[N+][C@H]5[C@H][C@@H]9OC=O)cc6cccc6)OCO5)))))))))))))[O-])C
Scaffold Graph/Node/Bond level: O=C1OC2CC=C3CC[NH2+]C3C2c2cc3c(cc21)OCO3
Scaffold Graph/Node level: OC1OC2CCC3CCNC3C2C2CC3OCOC3CC12
Scaffold Graph level: CC1CC2CCC3CCCC3C2C2CC3CCCC3CC12
Functional groups: CO; CC(=CC)C; C[N+](C)([O-])C; cC(=O)OC; c1cOCO1
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Alkaloids and derivatives
ClassyFire Class: Amaryllidaceae alkaloids
ClassyFire Subclass: Homolycorine-type amaryllidaceae alkaloids
Synonymous chemical names:
hippeastrine n-oxide
External chemical identifiers:
CID:CID_15071950; ChEMBL:CHEMBL2377309; ZINC:ZINC000096909154
Chemical structure download


Hippeastrine N-oxide
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 331.32
Log P RDKit 1.06
Topological polar surface area (Å2) RDKit 88.05
Number of hydrogen bond acceptors RDKit 6
Number of hydrogen bond donors RDKit 1
Number of carbon atoms RDKit 17
Number of heavy atoms RDKit 24
Number of heteroatoms RDKit 7
Number of nitrogen atoms RDKit 1
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 4
Stereochemical complexity RDKit 0.24
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 9
Number of sp3 hybridized carbon atoms RDKit 8
Shape complexity RDKit 0.47
Number of rotatable bonds RDKit 0
Number of aliphatic carbocycles RDKit 1
Number of aliphatic heterocycles RDKit 3
Number of aliphatic rings RDKit 4
Number of aromatic carbocycles RDKit 1
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 1
Total number of rings RDKit 5
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 1
Number of saturated rings RDKit 1
Number of Smallest Set of Smallest Rings (SSSR) RDKit 5


Hippeastrine N-oxide
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 Good
GSK 4/400 filter RDKit Good
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.330902


Hippeastrine N-oxide
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -8.15
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 2
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME No
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME Yes