Molecule Name DB06288
DrugBank Groups Approved
Cluster No 218
Smiles S(=O)(=O)(C1(=C(N)C=C(OC)C(=C1)C(=O)NCC2(N(CCC2)CC)))CC
Download mol2, pdbqt
TPSA 110,11
Non-H Atoms 25
Non-C/H Atoms 8
Metal-Atoms 0
Electronegative Atoms 8
Stereo Centers 1
Rotatable Bonds 7
Rings Closures 2
Small Rings 2
Aromatic Rings 1
Aromatic Atoms 6
sp3-Atoms 13
Symmetric atoms 1
cLogS -2,851
MW 369,484
cLogP 0,6656
HBA 7
HBD 2
Ro5 violations 0
Druglikeness 7,3468
DrugScore 0,860038119874924
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 Non-inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,344
Caco-2 Permeability 2 0,2921
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 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 Inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,482
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3342
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,4706
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.