Molecule Name DB02555
DrugBank Groups Experimental
Cluster No 627
Smiles ClC3(=C(Cl)C(C1(=NN(C)C(=C1)C2(CCN(C(=O)CNC(=O)C(N=C(N)N)CC(C)C)CC2)))=CC=C3OCC4(=CC=C(NC(=O)C)C=C4))
Download mol2, pdbqt
TPSA 517,42
Non-H Atoms 47
Non-C/H Atoms 14
Metal-Atoms 0
Electronegative Atoms 14
Stereo Centers 1
Rotatable Bonds 12
Rings Closures 4
Small Rings 4
Aromatic Rings 3
Aromatic Atoms 17
sp3-Atoms 15
Symmetric atoms 6
cLogS -7,017
MW 685,654
cLogP 3,735
HBA 12
HBD 4
Ro5 violations 2
Druglikeness 9,0128
DrugScore 9,82007409220356E-02
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 Inhibitor
P-glycoprotein Inhibitor 2 Inhibitor
Renal Organic Cation Transporter Inhibitor
Aqueous solubility -3,5474
Caco-2 Permeability 2 0,4331
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) 1,2655
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5779
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,671
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.