Molecule Name DB06785
DrugBank Groups Approved
Cluster No 1
Smiles ClC6(=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))CCCCN=C(NCC)NCC)CC(C)C)CCCCN=C(NCC)NCC)CC4(=CC=C(O)C=C4))CO)CC5(=CN=CC=C5))C=C6)
Download mol2, pdbqt
TPSA 451,49
Non-H Atoms 112
Non-C/H Atoms 32
Metal-Atoms 0
Electronegative Atoms 32
Stereo Centers 10
Rotatable Bonds 44
Rings Closures 6
Small Rings 6
Aromatic Rings 5
Aromatic Atoms 28
sp3-Atoms 42
Symmetric atoms 11
cLogS -10,817
MW 1570,34
cLogP 3,0013
HBA 31
HBD 16
Ro5 violations 3
Druglikeness 0,20921
DrugScore 0,109787520054687
Mutagenic none
Tumorigenic none
Reproductive Effective high
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 Inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,6225
Caco-2 Permeability 2 -0,3386
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) 1,4004
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5526
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,8022
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.