IMPPAT Phytochemical information: 
Aristoloside

Aristoloside
Summary

SMILES: OC[C@H]1O[C@@H](Oc2cc(OC)c3c(c2)c2c4OCOc4cc(c2c(c3)[N+](=O)[O-])C(=O)O)[C@@H]([C@H]([C@@H]1O)O)O
InChI: InChI=1S/C23H21NO13/c1-33-13-3-8(36-23-20(28)19(27)18(26)15(6-25)37-23)2-10-9(13)4-12(24(31)32)16-11(22(29)30)5-14-21(17(10)16)35-7-34-14/h2-5,15,18-20,23,25-28H,6-7H2,1H3,(H,29,30)/t15-,18-,19+,20-,23-/m1/s1
InChIKey: GMKHAVDYTAXBIY-BSTKLLGTSA-N
DeepSMILES: OC[C@H]O[C@@H]OcccOC))ccc6)ccOCOc5ccc9cc%13)[N+]=O)[O-]))))C=O)O))))))))))))))))[C@@H][C@H][C@@H]6O))O))O
Scaffold Graph/Node/Bond level: c1cc2ccc3ccc4c(c3c2cc1OC1CCCCO1)OCO4
Scaffold Graph/Node level: C1CCC(OC2CCC3CCC4CCC5OCOC5C4C3C2)OC1
Scaffold Graph level: C1CCC(CC2CCC3CCC4CCC5CCCC5C4C3C2)CC1
Functional groups: CO; cO[C@@H](C)OC; cOC; c1cOCO1; c[N+](=O)[O-]; cC(=O)O
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketides
ClassyFire Class: Tannins
ClassyFire Subclass: Hydrolyzable tannins
Synonymous chemical names:
aristololide
External chemical identifiers:
CID:CID_128576; ZINC:ZINC000139897358
Chemical structure download


Aristoloside
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 519.42
Log P RDKit 0.52
Topological polar surface area (Å2) RDKit 207.51
Number of hydrogen bond acceptors RDKit 12
Number of hydrogen bond donors RDKit 5
Number of carbon atoms RDKit 23
Number of heavy atoms RDKit 37
Number of heteroatoms RDKit 14
Number of nitrogen atoms RDKit 1
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 5
Stereochemical complexity RDKit 0.22
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 15
Number of sp3 hybridized carbon atoms RDKit 8
Shape complexity RDKit 0.35
Number of rotatable bonds RDKit 6
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 2
Number of aliphatic rings RDKit 2
Number of aromatic carbocycles RDKit 3
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 3
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


Aristoloside
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 2
Lipinski’s rule of 5 RDKit Failed
Number of Ghose rule violations RDKit 1
Ghose rule RDKit Failed
Veber rule RDKit Bad
Egan rule RDKit Bad
GSK 4/400 rule RDKit Bad
Pfizer 3/75 rule RDKit Good
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.17


Aristoloside
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.11
Solubility class [ESOL] SwissADME Soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME Low
Log Kp (Skin permeation, cm/s) SwissADME -8.47
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 3
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME Yes
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME Yes