Molecule Name DB02581
DrugBank Groups Experimental
Cluster No 627
Smiles ClC3(=C(Cl)C(C1(=NN(C)C(=C1)C2(CCN(C(=O)CNC(=O)C(NC(=N)N)CC(C)C)CC2)))=CC=C3OCC=4(OC(C(=O)O)=CC=4))
Download mol2, pdbqt
TPSA 490,02
Non-H Atoms 45
Non-C/H Atoms 15
Metal-Atoms 0
Electronegative Atoms 15
Stereo Centers 1
Rotatable Bonds 12
Rings Closures 4
Small Rings 4
Aromatic Rings 3
Aromatic Atoms 16
sp3-Atoms 15
Symmetric atoms 3
cLogS -5,434
MW 662,573
cLogP 3,1676
HBA 13
HBD 5
Ro5 violations 2
Druglikeness 9,4118
DrugScore 0,131260268065072
Mutagenic none
Tumorigenic none
Reproductive Effective high
Irritant high
Blood-Brain Barrier BBB-
Human Intestinal Absorption HIA+
Caco-2 Permeability Caco2-
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor Non-inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,314
Caco-2 Permeability 2 0,0185
Subcellular localization Mitochondria
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) 1,358
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5582
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6809
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.