Molecule Name DB01436
DrugBank Groups Approved
Cluster No 22
Smiles OC3(C(C(=CC=C2(C1(C(C(C(CCCC(C)C)C)CC1)(CCC2)C)))CC(C3)O)=C)
Download mol2, pdbqt
TPSA 40,46
Non-H Atoms 29
Non-C/H Atoms 2
Metal-Atoms 0
Electronegative Atoms 2
Stereo Centers 6
Rotatable Bonds 6
Rings Closures 3
Small Rings 3
Aromatic Rings 0
Aromatic Atoms 0
sp3-Atoms 23
Symmetric atoms 1
cLogS -5,596
MW 400,644
cLogP 6,8241
HBA 2
HBD 2
Ro5 violations 1
Druglikeness -4,6948
DrugScore 0,1720259291143
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 Inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,93
Caco-2 Permeability 2 1,2787
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) 0,2903
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 1,0393
Honey Bee Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity I
Rat Acute Toxicity (LD50, mol/kg) 4,6023
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.