Molecule Name DB02638
DrugBank Groups Approved
Cluster No 1
Smiles S1(SCC(NC(=O)C(NC(=O)C(NC(C(NC(C(NC(C(C1)NC(=O)CNC(=O)CNC(=O)CN)=O)CC2(=CC=C(O)C=C2))=O)CC3(=CC=CC=C3))=O)CCC(=O)N)CC(=O)N)C(=O)N4(C(C(=O)NC(C(=O)NCC(=O)N)CCCCN)CCC4))
Download mol2, pdbqt
TPSA 563,45
Non-H Atoms 85
Non-C/H Atoms 33
Metal-Atoms 0
Electronegative Atoms 33
Stereo Centers 8
Rotatable Bonds 25
Rings Closures 4
Small Rings 3
Aromatic Rings 2
Aromatic Atoms 12
sp3-Atoms 31
Symmetric atoms 4
cLogS -3,704
MW 1227,39
cLogP -7,5835
HBA 31
HBD 16
Ro5 violations 3
Druglikeness 7,0942
DrugScore 0,446176656849754
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 -2,7338
Caco-2 Permeability 2 -0,1982
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) 1,5886
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,2585
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,9218
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.