Molecule Name DB03333
DrugBank Groups Experimental
Cluster No 989
Smiles S(=O)(=O)(N)C2(=CC=C(NC(=S)OCCC1(=CSC=C1))C=C2)
Download mol2, pdbqt
TPSA 247,75
Non-H Atoms 21
Non-C/H Atoms 8
Metal-Atoms 0
Electronegative Atoms 8
Stereo Centers 0
Rotatable Bonds 6
Rings Closures 2
Small Rings 2
Aromatic Rings 2
Aromatic Atoms 11
sp3-Atoms 5
Symmetric atoms 3
cLogS -3,591
MW 342,463
cLogP 2,3598
HBA 5
HBD 2
Ro5 violations 0
Druglikeness 2,4232
DrugScore 0,781427936295589
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Blood-Brain Barrier BBB+
Human Intestinal Absorption HIA+
Caco-2 Permeability Caco2-
P-glycoprotein Substrate Non-substrate
P-glycoprotein Inhibitor Non-inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -2,4699
Caco-2 Permeability 2 0,6178
Subcellular localization Mitochondria
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Non-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 High 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 Low FHMT
Fish Toxicity (pLC50, mg/L) 1,9229
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,1586
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,2783
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.