Molecule Name DB03011
DrugBank Groups Experimental
Cluster No 138
Smiles S=P(S)(OCC3(OC(N2(C1(=NC=NC(=C1N=C2)N)))C(C3O)O))O
Download mol2, pdbqt
TPSA 245,76
Non-H Atoms 23
Non-C/H Atoms 13
Metal-Atoms 0
Electronegative Atoms 13
Stereo Centers 5
Rotatable Bonds 4
Rings Closures 3
Small Rings 3
Aromatic Rings 2
Aromatic Atoms 9
sp3-Atoms 13
Symmetric atoms 0
cLogS 1,551
MW 379,357
cLogP -1,9632
HBA 10
HBD 4
Ro5 violations 0
Druglikeness -10,687
DrugScore 0,104114448063144
Mutagenic high
Tumorigenic high
Reproductive Effective low
Irritant low
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 -3,0114
Caco-2 Permeability 2 -0,4371
Subcellular localization Mitochondria
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 Non-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 Non-inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,5721
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3823
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,2892
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.