Molecule Name DB00153
DrugBank Groups Approved
Cluster No 22
Smiles OC1(CC(C(=C)CC1)=CC=C3(C2(C(C(C(C=CC(C(C)C)C)C)CC2)(CCC3)C)))
Download mol2, pdbqt
TPSA 20,23
Non-H Atoms 29
Non-C/H Atoms 1
Metal-Atoms 0
Electronegative Atoms 1
Stereo Centers 6
Rotatable Bonds 5
Rings Closures 3
Small Rings 3
Aromatic Rings 0
Aromatic Atoms 0
sp3-Atoms 21
Symmetric atoms 1
cLogS -5,927
MW 396,656
cLogP 7,6423
HBA 1
HBD 1
Ro5 violations 1
Druglikeness -5,8133
DrugScore 0,121887015434529
Mutagenic none
Tumorigenic none
Reproductive Effective low
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 -4,5363
Caco-2 Permeability 2 1,635
Subcellular localization Lysosome
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 Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) -0,1791
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,9458
Honey Bee Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity I
Rat Acute Toxicity (LD50, mol/kg) 3,6931
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.