Molecule Name DB08213
DrugBank Groups Experimental
Cluster No 2469
Smiles S(=O)(=O)(N1(C(CCC1)COC2(=CC=CC=C2)))C4(=CC=3(C(=O)C(=O)N(C=3C=C4)C))
Download mol2, pdbqt
TPSA 280,5
Non-H Atoms 28
Non-C/H Atoms 8
Metal-Atoms 0
Electronegative Atoms 8
Stereo Centers 1
Rotatable Bonds 4
Rings Closures 4
Small Rings 4
Aromatic Rings 2
Aromatic Atoms 12
sp3-Atoms 8
Symmetric atoms 3
cLogS -3,317
MW 400,454
cLogP 1,7846
HBA 7
HBD 0
Ro5 violations 0
Druglikeness 1,3465
DrugScore 0,716362041569064
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 Inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,9854
Caco-2 Permeability 2 0,7609
Subcellular localization Mitochondria
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 1A2 Inhibitor Non-inhibitor
CYP450 2C9 Inhibitor Inhibitor
CYP450 2D6 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Inhibitor
CYP450 3A4 Inhibitor Inhibitor
CYP Inhibitory Promiscuity High CYP Inhibitory Promiscuity
Human Ether-a-go-go-Related Gene Inhibition Weak inhibitor
Human Ether-a-go-go-Related Gene Inhibition 2 Inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,5165
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4709
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,4657
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.