SMILES Oc(c(O)c1)cc2c1n(C(c1ccccc1)=O)c(cc1O)c2cc1O
Download 4096.mol2, BDB-kin4096.pdbqt
Total Surface Area 234,57
TPSA 102,92
cLogS -4,613
MW 335,314
cLogP 3,5198
H-Acceptors 6
H-Donors 4
Ro5 violations 0
Druglikeness 1,43
DrugScore 0,491314210200824
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant low
Human Intestinal Absorption HIA+
Blood-Brain Barrier BBB+
Caco-2 Permeability I Caco2-
Caco-2 Permeability II 0,6157
P-glycoprotein Substrate Non-substrate
P-glycoprotein Inhibitor I Non-inhibitor
P-glycoprotein Inhibitor II Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 1A2 Inhibitor 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
AMES Toxicity Non AMES toxic
Carcinogenicity (Three-class) Warning
Biodegradation Not ready biodegradable
Rat Acute Toxicity 2,436
hERG inhibition (predictor I) Weak inhibitor
hERG inhibition (predictor II) Non-inhibitor
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, mg/L) 0,2929
Fish Toxicity High FHMT
Fish Toxicity (pLC50 mg/L) 0,6662
Acute Oral Toxicity III
Carcinogens Non-carcinogens
Honey Bee Toxicity Low HBT
Subcellular localization Mitochondria
These data are only available for scientific research purposes.