Molecule Name DB01443
DrugBank Groups Experimental
Cluster No 6
Smiles O=C3(CC2(=CCC4(C1(C(C(=O)CC1)(C)CCC4(C2CC3)))))
Download mol2, pdbqt
TPSA 202,46
Non-H Atoms 20
Non-C/H Atoms 2
Metal-Atoms 0
Electronegative Atoms 2
Stereo Centers 5
Rotatable Bonds 0
Rings Closures 4
Small Rings 4
Aromatic Rings 0
Aromatic Atoms 0
sp3-Atoms 14
Symmetric atoms 0
cLogS -3,935
MW 272,387
cLogP 3,3084
HBA 2
HBD 0
Ro5 violations 0
Druglikeness 0,059585
DrugScore 0,590374402708464
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 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,9848
Caco-2 Permeability 2 1,6801
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) 0,1511
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,557
Honey Bee Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 1,6104
Carcinogenicity (Three-class) Warning
These data are only available for scientific research purposes.