Molecule Name DB00666
DrugBank Groups Approved
Cluster No 2
Smiles O=C8(NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1(C(C(=O)NCC(=O)N)CCC1))CCCN=C(N)N)CC(C)C)CC3(=CC=2(C(=CC=CC=2)C=C3)))CC4(=CC=C(O)C=C4))CO)CC=6(C5(=C(C=CC=C5)NC=6)))CC=7(NC=NC=7))CC8)
Download mol2, pdbqt
TPSA 474,63
Non-H Atoms 96
Non-C/H Atoms 30
Metal-Atoms 0
Electronegative Atoms 30
Stereo Centers 9
Rotatable Bonds 33
Rings Closures 8
Small Rings 8
Aromatic Rings 6
Aromatic Atoms 30
sp3-Atoms 29
Symmetric atoms 4
cLogS -7,834
MW 1322,49
cLogP -2,0536
HBA 30
HBD 16
Ro5 violations 3
Druglikeness 11,123
DrugScore 0,263776327163487
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 -3,2286
Caco-2 Permeability 2 -0,521
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 Non-inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,4977
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4256
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6799
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.