Molecule Name DB07967
DrugBank Groups Experimental
Cluster No 2318
Smiles O(C4(=C(NC1(=NC(=NC2(=C1N=CN2C3(CCCC3)))C#N))C=CC=C4))CCCN5(C=NC=C5)
Download mol2, pdbqt
TPSA 339,31
Non-H Atoms 32
Non-C/H Atoms 9
Metal-Atoms 0
Electronegative Atoms 9
Stereo Centers 0
Rotatable Bonds 8
Rings Closures 5
Small Rings 5
Aromatic Rings 4
Aromatic Atoms 20
sp3-Atoms 9
Symmetric atoms 2
cLogS -3,74
MW 428,499
cLogP 3,2425
HBA 9
HBD 1
Ro5 violations 0
Druglikeness -3,4477
DrugScore 0,361514541261164
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 -3,1244
Caco-2 Permeability 2 0,8716
Subcellular localization Mitochondria
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 1A2 Inhibitor Inhibitor
CYP450 2C9 Inhibitor 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 Strong 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) 1,3208
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4896
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,4423
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.