Molecule Name DB00362
DrugBank Groups Approved
Cluster No 195
Smiles O=C4(N7(C(C(=O)NC(O)C(O)CC(NC(=O)C3(=CC=C(C2(=CC=C(C1(=CC=C(OCCCCC)C=C1))C=C2))C=C3))C(=O)NC(C(N6(C(C(NC(C(NC4C(O)C)=O)C(O)C(O)C5(=CC=C(O)C=C5))=O)CC(O)C6))=O)C(O)C)C(O)C(C7)C))
Download mol2, pdbqt
TPSA 377,42
Non-H Atoms 82
Non-C/H Atoms 24
Metal-Atoms 0
Electronegative Atoms 24
Stereo Centers 15
Rotatable Bonds 14
Rings Closures 7
Small Rings 6
Aromatic Rings 4
Aromatic Atoms 24
sp3-Atoms 37
Symmetric atoms 8
cLogS -6,906
MW 1140,25
cLogP -0,4951
HBA 24
HBD 14
Ro5 violations 3
Druglikeness -1,5563
DrugScore 0,165506299924305
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 Inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,2132
Caco-2 Permeability 2 -0,1476
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 Inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,3469
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5421
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,7797
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.