Molecule Name DB02336
DrugBank Groups Experimental
Cluster No 83
Smiles P(=O)(O)(O)C1(=C(P(=O)(O)O)C=CC(=C1)CC(N=C(O)C)C(O)=NC2(C(=O)N(CCCC2)CC4(=CC=C(C3(=CC=CC=C3))C=C4)))
Download mol2, pdbqt
TPSA 458,73
Non-H Atoms 44
Non-C/H Atoms 14
Metal-Atoms 0
Electronegative Atoms 14
Stereo Centers 2
Rotatable Bonds 10
Rings Closures 4
Small Rings 4
Aromatic Rings 3
Aromatic Atoms 18
sp3-Atoms 17
Symmetric atoms 6
cLogS -2,507
MW 643,568
cLogP -3,2561
HBA 12
HBD 6
Ro5 violations 3
Druglikeness -7,436
DrugScore 0,277014644247837
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 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,3147
Caco-2 Permeability 2 -0,4752
Subcellular localization Mitochondria
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate 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) 1,4927
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4703
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,5874
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.