Molecule Name DB06196
DrugBank Groups Approved
Cluster No 360
Smiles S1(C(=CC=C1)CC(NC(=O)CNC(=O)C3(N(C(=O)C2(N(C(=O)C(NC(=O)C(N)CCCN=C(N)N)CCCN=C(N)N)CCC2))CC(C3)O))C(=O)NC(C(=O)N6(C(C(=O)N5(C4(C(CCCC4)CC5C(=O)NC(C(=O)O)CCCN=C(N)N)))CC=7(C=CC=CC=7(C6))))CO)
Download mol2, pdbqt
TPSA 551,96
Non-H Atoms 92
Non-C/H Atoms 33
Metal-Atoms 0
Electronegative Atoms 33
Stereo Centers 12
Rotatable Bonds 30
Rings Closures 7
Small Rings 7
Aromatic Rings 2
Aromatic Atoms 11
sp3-Atoms 40
Symmetric atoms 3
cLogS -5,948
MW 1304,54
cLogP -7,8966
HBA 32
HBD 15
Ro5 violations 3
Druglikeness -8,2734
DrugScore 0,159961762330573
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 -2,9943
Caco-2 Permeability 2 -0,4842
Subcellular localization Mitochondria
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
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) 1,5825
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4071
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,4262
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.