Molecule Name DB03208
DrugBank Groups Experimental
Cluster No 941
Smiles O=C(OC2(OC(C(OC(=O)C1(=CC(O)=C(O)C(=C1)O))C(C2OC(=O)C3(=CC(O)=C(O)C(=C3)O))OC(=O)C4(=CC(O)=C(O)C(=C4)O))COC(=O)C5(=CC(O)=C(O)C(=C5)O)))C6(=CC(O)=C(O)C(=C6)O)
Download mol2, pdbqt
TPSA 619,06
Non-H Atoms 67
Non-C/H Atoms 26
Metal-Atoms 0
Electronegative Atoms 26
Stereo Centers 5
Rotatable Bonds 16
Rings Closures 6
Small Rings 6
Aromatic Rings 5
Aromatic Atoms 30
sp3-Atoms 27
Symmetric atoms 15
cLogS -3,209
MW 940,679
cLogP 1,8357
HBA 26
HBD 15
Ro5 violations 3
Druglikeness -0,25527
DrugScore 0,328346783956249
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 Non-inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -1,7414
Caco-2 Permeability 2 -0,5874
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) 0,3433
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,6541
Honey Bee Toxicity High HBT
Biodegradation Ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,8451
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.