Molecule Name DB08755
DrugBank Groups Experimental
Cluster No 1173
Smiles O=C(N1(CCOCC1))NC(C(=O)NC(C#N)(COCC2(=CC=CC=C2))C)CC3(CCCCC3)
Download mol2, pdbqt
TPSA 369,48
Non-H Atoms 33
Non-C/H Atoms 8
Metal-Atoms 0
Electronegative Atoms 8
Stereo Centers 2
Rotatable Bonds 9
Rings Closures 3
Small Rings 3
Aromatic Rings 1
Aromatic Atoms 6
sp3-Atoms 18
Symmetric atoms 6
cLogS -3,955
MW 456,585
cLogP 2,1717
HBA 8
HBD 2
Ro5 violations 0
Druglikeness -4,6261
DrugScore 0,208425778210251
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant high
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 -3,583
Caco-2 Permeability 2 0,5003
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 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) 1,8558
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3565
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6242
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.