Molecule Name DB01347
DrugBank Groups Experimental
Cluster No 5
Smiles [Br]C1(=C(OC4(=C1C=C(CN3(C(=C(C2(CC2))N=C3CC)C(=O)N))C=C4))C5(=C(NS(=O)(=O)[C+](F)(F)F)C=CC=C5))
Download mol2, pdbqt
TPSA 388,82
Non-H Atoms 38
Non-C/H Atoms 13
Metal-Atoms 0
Electronegative Atoms 13
Stereo Centers 0
Rotatable Bonds 8
Rings Closures 5
Small Rings 5
Aromatic Rings 4
Aromatic Atoms 20
sp3-Atoms 8
Symmetric atoms 4
cLogS -7,482
MW 611,438
cLogP 5,98
HBA 8
HBD 2
Ro5 violations 2
Druglikeness 1,2308
DrugScore 0,110176100482785
Mutagenic none
Tumorigenic none
Reproductive Effective high
Irritant none
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 -3,7897
Caco-2 Permeability 2 0,4936
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 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 Inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,4675
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5823
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,5847
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.