Molecule Name DB00115
DrugBank Groups Approved
Cluster No 5
Smiles [Co-]1245(N=%10(C%11(=CC%12(=N1C(=C(C)C3(=N2C(C(CC(=O)N)(C)C3CCC(=O)N)(C)C9(N4C(C(CCC(=O)NCC(C)OP(OC8(C(C(N7(C=N5C6(=C7(C=C(C)C(=C6)C))))OC8(CO))O))(=O)O)(C)C9CC(=O)N)=C(C=%10C(CCC(=O)N)C%11(C)C)C)))C(CC(=O)N)(C)C%12CCC(=O)N))))(C#N)
Download mol2, pdbqt
TPSA 476,87
Non-H Atoms 93
Non-C/H Atoms 30
Metal-Atoms 1
Electronegative Atoms 29
Stereo Centers 15
Rotatable Bonds 16
Rings Closures 12
Small Rings 11
Aromatic Rings 2
Aromatic Atoms 9
sp3-Atoms 46
Symmetric atoms 1
cLogS -8,956
MW 1356,39
cLogP -1,8027
HBA 28
HBD 10
Ro5 violations 3
Druglikeness -30,202
DrugScore 0,127281241984075
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 -3,3475
Caco-2 Permeability 2 0,0051
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 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) 1,2452
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5835
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6929
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.