Molecule Name DB00626
DrugBank Groups Approved
Cluster No 360
Smiles S1(C(=NC(C1)C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC3(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(CC=2(N=CNC=2))C(NC(C(NC(C(NCCCC3)=O)CC(=O)N)=O)CC(=O)O)=O)CC4(=CC=CC=C4))C(CC)C)CCCN))C(CC)C)CCC(=O)O)CC(C)C)C(N)C(CC)C)
Download mol2, pdbqt
TPSA 556,17
Non-H Atoms 100
Non-C/H Atoms 34
Metal-Atoms 0
Electronegative Atoms 34
Stereo Centers 15
Rotatable Bonds 31
Rings Closures 4
Small Rings 3
Aromatic Rings 2
Aromatic Atoms 11
sp3-Atoms 47
Symmetric atoms 3
cLogS -6,14
MW 1422,71
cLogP -7,5135
HBA 33
HBD 17
Ro5 violations 3
Druglikeness 2,7215
DrugScore 0,301000252062144
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 -3,079
Caco-2 Permeability 2 -0,4297
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 Non-inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,7068
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3924
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,8201
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.