Molecule Name DB00006
DrugBank Groups Approved
Cluster No 1
Smiles O=C(NC(C(=O)N4(C(C(=O)NCC(=O)NCC(=O)NCC(=O)NCC(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2(C(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)O)CC(C)C)CC1(=CC=C(O)C=C1))CCC(=O)O)CCC(=O)O)CCC2))C(CC)C)CCC(=O)O)CCC(=O)O)CC3(=CC=CC=C3))CC(=O)O)CC(=O)N)CCC4))CCCNC(=N)N)C6(N(C(=O)C(N)CC5(=CC=CC=C5))CCC6)
Download mol2, pdbqt
TPSA 901,57
Non-H Atoms 155
Non-C/H Atoms 57
Metal-Atoms 0
Electronegative Atoms 57
Stereo Centers 16
Rotatable Bonds 66
Rings Closures 6
Small Rings 6
Aromatic Rings 3
Aromatic Atoms 18
sp3-Atoms 61
Symmetric atoms 7
cLogS -5,228
MW 2180,31
cLogP -11,245
HBA 57
HBD 28
Ro5 violations 3
Druglikeness -7,0493
DrugScore 0,180562152451813
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 -3,4444
Caco-2 Permeability 2 -0,6633
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) 1,5463
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3899
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 3,1654
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.