Molecule Name DB01111
DrugBank Groups Approved
Cluster No 4
Smiles S(=O)(=O)(O)CNCCC1(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(C(CCNC(C(NC1=O)C(O)C)=O)NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)CCCCC(CC)C)CCNCS(=O)(=O)O)C(O)C)CCNCS(=O)(=O)O)=O)CCNCS(=O)(=O)O)CC(C)C)CC(C)C)CCNCS(=O)(=O)O)
Download mol2, pdbqt
TPSA 734,46
Non-H Atoms 107
Non-C/H Atoms 49
Metal-Atoms 0
Electronegative Atoms 49
Stereo Centers 13
Rotatable Bonds 44
Rings Closures 1
Small Rings 0
Aromatic Rings 0
Aromatic Atoms 0
sp3-Atoms 64
Symmetric atoms 7
cLogS -4,174
MW 1639,93
cLogP -21,816
HBA 44
HBD 23
Ro5 violations 3
Druglikeness -5,2594
DrugScore 0,213034859386003
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 -3,0493
Caco-2 Permeability 2 0,1593
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) 1,6308
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3235
Honey Bee Toxicity Low HBT
Biodegradation Ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6104
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.