Molecule Name DB00256
DrugBank Groups Approved
Cluster No 113
Smiles O=C2(C1(=C(O)C=CC=C1C(O)(C)C4(C2=C(O)C3(O)(C(=O)C(=C(O)C(C3C4)N(C)C)C(=O)NCNCCCCC(N)C(=O)O))))
Download mol2, pdbqt
TPSA 242,98
Non-H Atoms 43
Non-C/H Atoms 14
Metal-Atoms 0
Electronegative Atoms 14
Stereo Centers 6
Rotatable Bonds 10
Rings Closures 4
Small Rings 4
Aromatic Rings 1
Aromatic Atoms 6
sp3-Atoms 24
Symmetric atoms 1
cLogS -2,591
MW 602,639
cLogP -6,2313
HBA 14
HBD 9
Ro5 violations 3
Druglikeness -10,552
DrugScore 0,293837852781907
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 -2,7066
Caco-2 Permeability 2 0,0859
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 Inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,1786
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4468
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,5422
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.