SMILES OC(CCC(CCC(O)=O)(c(cccc1)c1N1)C1=S)=O
Download 3968.mol2, BDB-kin3968.pdbqt
Total Surface Area 217,58
TPSA 118,72
cLogS -3,631
MW 293,342
cLogP 0,7043
H-Acceptors 5
H-Donors 3
Ro5 violations 0
Druglikeness -1,0967
DrugScore 0,321872420500866
Mutagenic none
Tumorigenic none
Reproductive Effective high
Irritant none
Human Intestinal Absorption HIA-
Blood-Brain Barrier BBB+
Caco-2 Permeability I Caco2-
Caco-2 Permeability II 0,604
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 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
AMES Toxicity Non AMES toxic
Carcinogenicity (Three-class) Non-required
Biodegradation Not ready biodegradable
Rat Acute Toxicity 2,552
hERG inhibition (predictor I) Weak inhibitor
hERG inhibition (predictor II) Non-inhibitor
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, mg/L) 0,3268
Fish Toxicity High FHMT
Fish Toxicity (pLC50 mg/L) 1,3599
Acute Oral Toxicity III
Carcinogens Non-carcinogens
Honey Bee Toxicity Low HBT
Subcellular localization Mitochondria
These data are only available for scientific research purposes.