Molecule Name DB00080
DrugBank Groups Approved
Cluster No 3
Smiles O=C3(OC(C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)CCCCCCCCC)CC=2(C1(=C(C=CC=C1)NC=2)))CC(=O)N)CC(=O)O)C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C)C(NC(C(NCC(NC(C(NC(C(NC3CC(=O)C4(=C(N)C=CC=C4))=O)C(CC(=O)O)C)=O)CO)=O)=O)CC(=O)O)=O)CC(=O)O)CCCN)C)
Download mol2, pdbqt
TPSA 702,02
Non-H Atoms 115
Non-C/H Atoms 43
Metal-Atoms 0
Electronegative Atoms 43
Stereo Centers 13
Rotatable Bonds 35
Rings Closures 4
Small Rings 3
Aromatic Rings 3
Aromatic Atoms 15
sp3-Atoms 45
Symmetric atoms 0
cLogS -6,255
MW 1620,69
cLogP -9,499
HBA 43
HBD 22
Ro5 violations 3
Druglikeness -17,937
DrugScore 0,152729658839434
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 -3,6856
Caco-2 Permeability 2 -0,0041
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) 1,2732
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5111
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,9781
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.