Molecule Name DB00146
DrugBank Groups Approved
Cluster No 22
Smiles OC(CCCC(C3(C2(C(C(=CC=C1(C(=C)CCC(C1)O))CCC2)CC3)(C)))C)(C)C
Download mol2, pdbqt
TPSA 40,46
Non-H Atoms 29
Non-C/H Atoms 2
Metal-Atoms 0
Electronegative Atoms 2
Stereo Centers 5
Rotatable Bonds 6
Rings Closures 3
Small Rings 3
Aromatic Rings 0
Aromatic Atoms 0
sp3-Atoms 23
Symmetric atoms 1
cLogS -5,545
MW 400,644
cLogP 6,8167
HBA 2
HBD 2
Ro5 violations 1
Druglikeness -5,354
DrugScore 0,172905519353142
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 Inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -4,4276
Caco-2 Permeability 2 1,4574
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 Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 0,0567
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 1,1261
Honey Bee Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity I
Rat Acute Toxicity (LD50, mol/kg) 4,1429
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.