Molecule Name DB00466
DrugBank Groups Experimental
Cluster No 1
Smiles O=C1(OC4(C5(OC(=O)C(C3(C4(C12(OC2C3))(C))(O))C5C(O)(C)C)))
Download mol2, pdbqt
TPSA 186,53
Non-H Atoms 22
Non-C/H Atoms 7
Metal-Atoms 0
Electronegative Atoms 7
Stereo Centers 8
Rotatable Bonds 1
Rings Closures 5
Small Rings 7
Aromatic Rings 0
Aromatic Atoms 0
sp3-Atoms 18
Symmetric atoms 1
cLogS -1,759
MW 310,301
cLogP -1,7499
HBA 7
HBD 2
Ro5 violations 0
Druglikeness 1,0596
DrugScore 0,488779558261595
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant high
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 -3,4304
Caco-2 Permeability 2 0,5988
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 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 AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,1943
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,587
Honey Bee Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,9546
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.