Molecule Name DB11592
DrugBank Groups Experimental
Cluster No 1277
Smiles S1(C3(N(C(C(=O)O)=C(C1)C=CC2(=C([N+](=O)[O-])C=C([N+](=O)[O-])C=C2))C(=O)C3NC(=O)CC=4(SC=CC=4)))
Download mol2, pdbqt
TPSA 350,09
Non-H Atoms 35
Non-C/H Atoms 14
Metal-Atoms 0
Electronegative Atoms 14
Stereo Centers 2
Rotatable Bonds 8
Rings Closures 4
Small Rings 4
Aromatic Rings 2
Aromatic Atoms 11
sp3-Atoms 8
Symmetric atoms 0
cLogS -4,625
MW 516,51
cLogP 0,9631
HBA 12
HBD 2
Ro5 violations 2
Druglikeness 7,3172
DrugScore 0,572393606885751
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 Non-inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -2,8161
Caco-2 Permeability 2 0,1207
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 AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,2747
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,576
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,3324
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.