Molecule Name DB07288
DrugBank Groups Experimental
Cluster No 1838
Smiles ClC3(=CC=C(NC(=O)C2(=C(NCC1(=CC=NC=C1))C=CC=C2))C=C3)
Download mol2, pdbqt
TPSA 261,39
Non-H Atoms 24
Non-C/H Atoms 5
Metal-Atoms 0
Electronegative Atoms 5
Stereo Centers 0
Rotatable Bonds 5
Rings Closures 3
Small Rings 3
Aromatic Rings 3
Aromatic Atoms 18
sp3-Atoms 1
Symmetric atoms 4
cLogS -4,452
MW 337,809
cLogP 3,4773
HBA 4
HBD 2
Ro5 violations 0
Druglikeness 1,32
DrugScore 0,623741651459334
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Blood-Brain Barrier BBB+
Human Intestinal Absorption HIA+
Caco-2 Permeability Caco2-
P-glycoprotein Substrate Non-substrate
P-glycoprotein Inhibitor Non-inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,6405
Caco-2 Permeability 2 1,1421
Subcellular localization Mitochondria
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Non-substrate
CYP450 1A2 Inhibitor Inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor 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 AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity Low FHMT
Fish Toxicity (pLC50, mg/L) 1,4141
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,7753
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 1,996
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.