Molecule Name DB02653
DrugBank Groups Experimental
Cluster No 678
Smiles FC1(C(F)C(C(F)C(C1NC3(C2(CC4(CC(C2)CC3C4))))F)C7(C(F)C(F)C(CC5(CC([N-]CC5)C6([N-]CCC(=C6)C)))C(C7F)F))
Download mol2, pdbqt
TPSA 419,59
Non-H Atoms 45
Non-C/H Atoms 11
Metal-Atoms 0
Electronegative Atoms 11
Stereo Centers 15
Rotatable Bonds 6
Rings Closures 7
Small Rings 8
Aromatic Rings 0
Aromatic Atoms 0
sp3-Atoms 35
Symmetric atoms 5
cLogS -8,603
MW 649,752
cLogP 4,4251
HBA 3
HBD 1
Ro5 violations 1
Druglikeness -0,4895
DrugScore 0,165841325174167
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 Inhibitor
Aqueous solubility -3,5442
Caco-2 Permeability 2 0,9922
Subcellular localization Lysosome
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 Non-inhibitor
CYP450 2C19 Inhibitor Non-inhibitor
CYP450 3A4 Inhibitor Non-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) 1,2554
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,8857
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,7101
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.