Molecule Name DB01809
DrugBank Groups Experimental
Cluster No 176
Smiles N3(=C(N)C1(=C(N(C(C)(C)C)N=C1C2(=CC=C(C)C=C2))N=C3))
Download mol2, pdbqt
TPSA 221,07
Non-H Atoms 21
Non-C/H Atoms 5
Metal-Atoms 0
Electronegative Atoms 5
Stereo Centers 0
Rotatable Bonds 2
Rings Closures 3
Small Rings 3
Aromatic Rings 3
Aromatic Atoms 15
sp3-Atoms 5
Symmetric atoms 4
cLogS -5,349
MW 281,362
cLogP 2,3935
HBA 5
HBD 1
Ro5 violations 0
Druglikeness 1,4959
DrugScore 0,599094094015631
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Blood-Brain Barrier BBB+
Human Intestinal Absorption HIA+
Caco-2 Permeability Caco2+
P-glycoprotein Substrate Non-substrate
P-glycoprotein Inhibitor Non-inhibitor
P-glycoprotein Inhibitor 2 Inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,926
Caco-2 Permeability 2 1,1662
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 Non-inhibitor
CYP450 2C19 Inhibitor 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 Non-inhibitor
AMES Toxicity AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 0,974
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,6834
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,3339
Carcinogenicity (Three-class) Danger
These data are only available for scientific research purposes.