Molecule Name DB06967
DrugBank Groups Experimental
Cluster No 1683
Smiles O(CCCN3(C1(=C(C=CC(=C1)C2(=C(N=C(N)N=C2CC)N))C4(=C3C=CC=C4))))C
Download mol2, pdbqt
TPSA 295,54
Non-H Atoms 28
Non-C/H Atoms 6
Metal-Atoms 0
Electronegative Atoms 6
Stereo Centers 0
Rotatable Bonds 6
Rings Closures 4
Small Rings 4
Aromatic Rings 4
Aromatic Atoms 19
sp3-Atoms 7
Symmetric atoms 0
cLogS -5,758
MW 375,475
cLogP 3,6361
HBA 6
HBD 2
Ro5 violations 0
Druglikeness 0,84411
DrugScore 0,131677505217664
Mutagenic high
Tumorigenic low
Reproductive Effective high
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 -3,2013
Caco-2 Permeability 2 0,6093
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 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) 1,3434
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3688
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6757
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.