IMPPAT Phytochemical information: 
1,3-Cyclobutanedicarboxylic acid, 2,4-diphenyl-, bis[(1r,2r,3s,5s)-2-(methoxycarbonyl)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl] ester, (1alpha,2alpha,3beta,4beta)-
1,3-Cyclobutanedicarboxylic acid, 2,4-diphenyl-, bis[(1r,2r,3s,5s)-2-(methoxycarbonyl)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl] ester, (1alpha,2alpha,3beta,4beta)-
Summary

SMILES: COC(=O)[C@H]1[C@H](C[C@H]2N([C@@H]1CC2)C)OC(=O)C1C(c2ccccc2)C(C1c1ccccc1)C(=O)O[C@H]1C[C@@H]2CC[C@H]([C@H]1C(=O)OC)N2C
InChI: InChI=1S/C38H46N2O8/c1-39-23-15-17-25(39)31(35(41)45-3)27(19-23)47-37(43)33-29(21-11-7-5-8-12-21)34(30(33)22-13-9-6-10-14-22)38(44)48-28-20-24-16-18-26(40(24)2)32(28)36(42)46-4/h5-14,23-34H,15-20H2,1-4H3/t23-,24-,25+,26+,27-,28-,29?,30?,31+,32+,33?,34?/m0/s1
InChIKey: BUOSLGZEBFSUDD-BGPZCGNYSA-N
DeepSMILES: COC=O)[C@H][C@H]C[C@H]N[C@@H]6CC5)))C))))OC=O)CCcccccc6))))))CC4cccccc6)))))))C=O)O[C@H]C[C@@H]CC[C@H][C@H]7C=O)OC))))N5C
Scaffold Graph/Node/Bond level: O=C(OC1CC2CCC(C1)N2)C1C(c2ccccc2)C(C(=O)OC2CC3CCC(C2)N3)C1c1ccccc1
Scaffold Graph/Node level: OC(OC1CC2CCC(C1)N2)C1C(C2CCCCC2)C(C(O)OC2CC3CCC(C2)N3)C1C1CCCCC1
Scaffold Graph level: CC(CC1CC2CCC(C2)C1)C1C(C2CCCCC2)C(C(C)CC2CC3CCC(C3)C2)C1C1CCCCC1
Functional groups: CC(=O)OC; COC(C)=O; CN(C)C
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organic acids and derivatives
ClassyFire Class: Carboxylic acids and derivatives
ClassyFire Subclass: Tetracarboxylic acids and derivatives
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Ornithine alkaloids
NP Classifier Class: Tropane alkaloids
Synonymous chemical names:
1,3-cyclobutanedicarboxylic acid, 2,4-diphenyl-, bis[(1r,2r,3s,5s)-2-(methoxycarbonyl)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl] ester, (1alpha,2alpha,3beta,4beta)-, alpha-truxilline
External chemical identifiers:
CID:CID_94155
Chemical structure download
2D:2D MOL2D MOL22D SDF
3D:3D MOL3D MOL23D SDF3D PDB3D PDBQT
1,3-Cyclobutanedicarboxylic acid, 2,4-diphenyl-, bis[(1r,2r,3s,5s)-2-(methoxycarbonyl)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl] ester, (1alpha,2alpha,3beta,4beta)-
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 658.79
Log P RDKit 3.94
Topological polar surface area (Å2) RDKit 111.68
Number of hydrogen bond acceptors RDKit 10
Number of hydrogen bond donors RDKit 0
Number of carbon atoms RDKit 38
Number of heavy atoms RDKit 48
Number of heteroatoms RDKit 10
Number of nitrogen atoms RDKit 2
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 8
Stereochemical complexity RDKit 0.21
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 16
Number of sp3 hybridized carbon atoms RDKit 22
Shape complexity RDKit 0.58
Number of rotatable bonds RDKit 12
Number of aliphatic carbocycles RDKit 1
Number of aliphatic heterocycles RDKit 4
Number of aliphatic rings RDKit 5
Number of aromatic carbocycles RDKit 2
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 2
Total number of rings RDKit 7
Number of saturated carbocycles RDKit 1
Number of saturated heterocycles RDKit 4
Number of saturated rings RDKit 5
Number of Smallest Set of Smallest Rings (SSSR) RDKit 7
1,3-Cyclobutanedicarboxylic acid, 2,4-diphenyl-, bis[(1r,2r,3s,5s)-2-(methoxycarbonyl)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl] ester, (1alpha,2alpha,3beta,4beta)-
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 1
Lipinski’s rule of 5 RDKit Passed
Number of Ghose rule violations RDKit 3
Ghose rule RDKit Failed
Veber rule RDKit Bad
Egan rule RDKit Good
GSK 4/400 rule RDKit Bad
Pfizer 3/75 rule RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.31
1,3-Cyclobutanedicarboxylic acid, 2,4-diphenyl-, bis[(1r,2r,3s,5s)-2-(methoxycarbonyl)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl] ester, (1alpha,2alpha,3beta,4beta)-
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Poorly soluble
Solubility class [Silicos-IT] SwissADME Moderately soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -7.02
Number of PAINS structural alerts SwissADME 0.0
Number of Brenk structural alerts SwissADME 1.0
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME Yes
CYP2C9 inhibitor SwissADME Yes
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME Yes
P-glycoprotein substrate SwissADME Yes