Molecule Name DB07021
DrugBank Groups Experimental
Cluster No 1726
Smiles FC4(=C(F)C=C(C1(C(N)CN2(C=3(C=CN=CC=3(N=C2(C1))))))C(=C4)F)
Download mol2, pdbqt
TPSA 220,93
Non-H Atoms 23
Non-C/H Atoms 7
Metal-Atoms 0
Electronegative Atoms 7
Stereo Centers 2
Rotatable Bonds 1
Rings Closures 4
Small Rings 4
Aromatic Rings 3
Aromatic Atoms 15
sp3-Atoms 5
Symmetric atoms 0
cLogS -2,425
MW 318,301
cLogP 2,6327
HBA 4
HBD 1
Ro5 violations 0
Druglikeness 2,2467
DrugScore 0,834507332109436
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 Non-inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,1962
Caco-2 Permeability 2 0,9991
Subcellular localization Lysosome
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Non-substrate
CYP450 1A2 Inhibitor Inhibitor
CYP450 2C9 Inhibitor Non-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 AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,3831
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,7448
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity II
Rat Acute Toxicity (LD50, mol/kg) 2,786
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.