Molecule Name DB00364
DrugBank Groups Approved
Cluster No 197
Smiles S(=O)(=O)(O[Al](O)O)OC1(C(OC(COS(=O)(=O)O[Al](O)O)C(C1OS(=O)(=O)O[Al](O)O)OS(=O)(=O)O[Al](O)O)OC2(OC(OS(=O)(=O)O[Al](O)O)C(C2OS(=O)(=O)O[Al](O)O)OS(=O)(=O)O[Al](O)O)(COS(=O)(=O)O[Al](O)O))
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TPSA 839,21
Non-H Atoms 78
Non-C/H Atoms 67
Metal-Atoms 8
Electronegative Atoms 59
Stereo Centers 9
Rotatable Bonds 36
Rings Closures 2
Small Rings 2
Aromatic Rings 0
Aromatic Atoms 0
sp3-Atoms 54
Symmetric atoms 16
cLogS 27,107
MW 1448,68
cLogP -6,9507
HBA 51
HBD 16
Ro5 violations 3
Druglikeness -4,6223
DrugScore 4,36208843753884E-02
Mutagenic high
Tumorigenic low
Reproductive Effective high
Irritant high
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 -2,2703
Caco-2 Permeability 2 -0,561
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 Non-carcinogens
Fish Toxicity Low FHMT
Fish Toxicity (pLC50, mg/L) 1,7348
Tetrahymena Pyriformis Toxicity Low TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,0267
Honey Bee Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,4219
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.