Molecule Name DB04389
DrugBank Groups Experimental
Cluster No 63
Smiles S=P(OP(=O)(O)CP(=O)(OCC3(OC(N2(C1(=NC=NC(=C1N=C2)N)))C(C3O)O))O)(OCC6(OC(N5(C4(=NC=NC(=C4N=C5)N)))C(C6O)O))O
Download mol2, pdbqt
TPSA 485,22
Non-H Atoms 49
Non-C/H Atoms 28
Metal-Atoms 0
Electronegative Atoms 28
Stereo Centers 11
Rotatable Bonds 12
Rings Closures 6
Small Rings 6
Aromatic Rings 4
Aromatic Atoms 18
sp3-Atoms 27
Symmetric atoms 0
cLogS -5,299
MW 770,505
cLogP -7,5781
HBA 24
HBD 9
Ro5 violations 3
Druglikeness -29,955
DrugScore 4,26016063255287E-02
Mutagenic low
Tumorigenic high
Reproductive Effective low
Irritant high
Blood-Brain Barrier BBB+
Human Intestinal Absorption HIA-
Caco-2 Permeability Caco2-
P-glycoprotein Substrate Non-substrate
P-glycoprotein Inhibitor Non-inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,3423
Caco-2 Permeability 2 -0,3113
Subcellular localization Lysosome
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Non-substrate
CYP450 1A2 Inhibitor Non-inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Non-inhibitor
CYP450 3A4 Inhibitor Inhibitor
CYP Inhibitory Promiscuity Low 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) 1,5076
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4574
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6673
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.