Molecule Name DB09099
DrugBank Groups Approved
Cluster No 3
Smiles S1(SCC(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(C1)NC(=O)CNC(=O)C(N)C)=O)CCCCN)=O)CC(=O)N)=O)CC2(=CC=CC=C2))=O)CC3(=CC=CC=C3))=O)CC=5(C4(=C(C=CC=C4)NC=5)))=O)CCCCN)C(O)C)CC6(=CC=CC=C6))C(O)C)CO)C(=O)O)
Download mol2, pdbqt
TPSA 663,83
Non-H Atoms 115
Non-C/H Atoms 39
Metal-Atoms 0
Electronegative Atoms 39
Stereo Centers 15
Rotatable Bonds 26
Rings Closures 6
Small Rings 5
Aromatic Rings 5
Aromatic Atoms 27
sp3-Atoms 44
Symmetric atoms 6
cLogS -7,642
MW 1637,9
cLogP -11,007
HBA 37
HBD 22
Ro5 violations 3
Druglikeness -3,5795
DrugScore 0,136927728218048
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 -3,2335
Caco-2 Permeability 2 -0,3379
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) 1,5254
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3757
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,8968
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.