Molecule Name DB01336
DrugBank Groups Approved
Cluster No 704
Smiles O4(C1(=C(OC)C=C2(CCN(C(C2(=C1))CC3(=CC=C(C=C3)OC7(=C6(C(CC5(=CC4=C(OC)C=C5))N(CCC6=CC(=C7OC)OC)(C)C))))(C)C)))
Download mol2, pdbqt
TPSA 61,86
Non-H Atoms 48
Non-C/H Atoms 8
Metal-Atoms 0
Electronegative Atoms 8
Stereo Centers 2
Rotatable Bonds 4
Rings Closures 7
Small Rings 6
Aromatic Rings 4
Aromatic Atoms 24
sp3-Atoms 24
Symmetric atoms 4
cLogS -6,804
MW 652,829
cLogP 4,3494
HBA 8
HBD 0
Ro5 violations 1
Druglikeness 6,1152
DrugScore 0,268701606338002
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Blood-Brain Barrier BBB+
Human Intestinal Absorption HIA+
Caco-2 Permeability Caco2+
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor Inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,0001
Caco-2 Permeability 2 1,5182
Subcellular localization Lysosome
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 1A2 Inhibitor Non-inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Non-inhibitor
CYP450 3A4 Inhibitor Non-inhibitor
CYP Inhibitory Promiscuity Low CYP Inhibitory Promiscuity
Human Ether-a-go-go-Related Gene Inhibition Weak inhibitor
Human Ether-a-go-go-Related Gene Inhibition 2 Non-inhibitor
AMES Toxicity AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,094
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,6626
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,7193
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.