Molecule Name DB06916
DrugBank Groups Experimental
Cluster No 1649
Smiles O=C(NCCC2(=CC=1(OCOC=1C=C2)))C5(N(C3(=NC(=NC(=C3)C)N4(C=NC=C4)))CCC5)
Download mol2, pdbqt
TPSA 318,09
Non-H Atoms 31
Non-C/H Atoms 9
Metal-Atoms 0
Electronegative Atoms 9
Stereo Centers 1
Rotatable Bonds 6
Rings Closures 5
Small Rings 5
Aromatic Rings 3
Aromatic Atoms 17
sp3-Atoms 10
Symmetric atoms 0
cLogS -3,966
MW 420,472
cLogP 2,5583
HBA 9
HBD 1
Ro5 violations 0
Druglikeness 6,3739
DrugScore 0,717517945991592
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 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,5077
Caco-2 Permeability 2 1,1846
Subcellular localization Mitochondria
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate 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 Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,4284
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,433
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,4056
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.