Molecule Name DB07340
DrugBank Groups Experimental
Cluster No 1936
Smiles O5(CCN(C4(=CC=C(NC2(=NC(NC1(CCCCC1))=C3(N=CNC3(=N2))))C=C4))CC5)
Download mol2, pdbqt
TPSA 306,03
Non-H Atoms 29
Non-C/H Atoms 8
Metal-Atoms 0
Electronegative Atoms 8
Stereo Centers 0
Rotatable Bonds 5
Rings Closures 5
Small Rings 5
Aromatic Rings 3
Aromatic Atoms 15
sp3-Atoms 11
Symmetric atoms 6
cLogS -5,779
MW 393,493
cLogP 3,1019
HBA 8
HBD 3
Ro5 violations 0
Druglikeness -3,0895
DrugScore 0,102841680509258
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 Non-inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -2,8451
Caco-2 Permeability 2 0,7712
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 Non-inhibitor
CYP450 3A4 Inhibitor Non-inhibitor
CYP Inhibitory Promiscuity Low CYP Inhibitory Promiscuity
Human Ether-a-go-go-Related Gene Inhibition Strong 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) 1,8004
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3814
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,3133
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.