Molecule Name DB06699
DrugBank Groups Approved
Cluster No 1
Smiles ClC8(=CC=C(CC(NC(=O)C(NC(=O)C)CC2(=CC=1(C(=CC=CC=1)C=C2)))C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N3(C(C(=O)NC(C(=O)N)C)CCC3))CCCCNC(C)C)CC(C)C)CC4(=CC=C(NC(=O)N)C=C4))CC6(=CC=C(NC(=O)C5(NC(=O)NC(C5)=O))C=C6))CO)CC7(=CN=CC=C7))C=C8)
Download mol2, pdbqt
TPSA 512,87
Non-H Atoms 117
Non-C/H Atoms 35
Metal-Atoms 0
Electronegative Atoms 35
Stereo Centers 11
Rotatable Bonds 41
Rings Closures 8
Small Rings 8
Aromatic Rings 6
Aromatic Atoms 34
sp3-Atoms 36
Symmetric atoms 8
cLogS -11,766
MW 1632,28
cLogP 1,0736
HBA 34
HBD 17
Ro5 violations 3
Druglikeness 1,2963
DrugScore 0,132749372602841
Mutagenic none
Tumorigenic high
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 -3,8055
Caco-2 Permeability 2 -0,1736
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 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) 1,4223
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5622
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,7005
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.