Molecule Name DB09265
DrugBank Groups Approved
Cluster No 2
Smiles S(CCC(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)CN=C(O)C(N=C(O)CN=C(O)C(N)CC=1(NC=NC=1))CCC(=O)O)C(O)C)CC2(=CC=CC=C2))C(O)C)CO)CC(=O)O)CC(C)C)CO)CCCCN)CCC(O)=N)C(O)=NC(C(O)=NC(C(O)=NC(C(O)=NC(C(O)=NC(C(O)=NC(C(O)=NC(C(O
Download mol2, pdbqt
TPSA 2228
Non-H Atoms 342
Non-C/H Atoms 127
Metal-Atoms 0
Electronegative Atoms 127
Stereo Centers 42
Rotatable Bonds 169
Rings Closures 8
Small Rings 8
Aromatic Rings 5
Aromatic Atoms 26
sp3-Atoms 205
Symmetric atoms 8
cLogS -12,271
MW 4858,55
cLogP -35,111
HBA 126
HBD 73
Ro5 violations 3
Druglikeness 7,5275
DrugScore 0,200085169999888
Mutagenic none
Tumorigenic none
Reproductive Effective low
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 -3,3975
Caco-2 Permeability 2 -0,4974
Subcellular localization Lysosome
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 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) 1,4687
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5195
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,9415
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.