Molecule Name DB06636
DrugBank Groups Approved
Cluster No 921
Smiles S1(C(=NC(=C1)C2(=CC=C(C#N)C=C2))C(C(O)(C3(=C(F)C=CC(=C3)F))CN4(N=CN(=C4)C(OC(=O)N(C5(=NC=CC=C5COC(=O)CNC))C)C))C)
Download mol2, pdbqt
TPSA 188,66
Non-H Atoms 51
Non-C/H Atoms 16
Metal-Atoms 0
Electronegative Atoms 16
Stereo Centers 3
Rotatable Bonds 15
Rings Closures 5
Small Rings 5
Aromatic Rings 5
Aromatic Atoms 28
sp3-Atoms 14
Symmetric atoms 2
cLogS -7,528
MW 717,776
cLogP 3,7365
HBA 13
HBD 2
Ro5 violations 2
Druglikeness -8,0133
DrugScore 0,12764741414274
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 Inhibitor
P-glycoprotein Inhibitor 2 Inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,5724
Caco-2 Permeability 2 0,5502
Subcellular localization Lysosome
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 Non-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) 1,3085
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,6396
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,7038
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.