Molecule Name DB01133
DrugBank Groups Approved
Cluster No 672
Smiles ClC1(=CC=C(SC(P(=O)(O)O)P(=O)(O)O)C=C1)
Download mol2, pdbqt
TPSA 159,98
Non-H Atoms 17
Non-C/H Atoms 10
Metal-Atoms 0
Electronegative Atoms 10
Stereo Centers 0
Rotatable Bonds 4
Rings Closures 1
Small Rings 1
Aromatic Rings 1
Aromatic Atoms 6
sp3-Atoms 8
Symmetric atoms 7
cLogS -2,444
MW 318,609
cLogP -4,5017
HBA 6
HBD 4
Ro5 violations 0
Druglikeness -11,721
DrugScore 0,457431801850082
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 -3,4721
Caco-2 Permeability 2 -0,3374
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 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 Carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,0197
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4802
Honey Bee Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,9059
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.