Molecule Name DB07362
DrugBank Groups Experimental
Cluster No 1948
Smiles S1(C(=NC=C1CCNC2(=NC=NC3(=C2N(N=C3)C)))NC(=O)NC4(=CC(=CC=C4)C(F)(F)F))
Download mol2, pdbqt
TPSA 328,93
Non-H Atoms 32
Non-C/H Atoms 13
Metal-Atoms 0
Electronegative Atoms 13
Stereo Centers 0
Rotatable Bonds 7
Rings Closures 4
Small Rings 4
Aromatic Rings 4
Aromatic Atoms 20
sp3-Atoms 4
Symmetric atoms 2
cLogS -5,444
MW 462,459
cLogP 3,1419
HBA 9
HBD 3
Ro5 violations 0
Druglikeness -1,6507
DrugScore 0,10914587461321
Mutagenic high
Tumorigenic high
Reproductive Effective none
Irritant none
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 Non-inhibitor
Aqueous solubility -3,726
Caco-2 Permeability 2 0,356
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 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) 1,4866
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5776
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,5932
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.