Molecule Name DB02920
DrugBank Groups Experimental
Cluster No 55
Smiles [Zn]135(N7(C8(=C(O)C=2(N1C(=C(CCC(=O)O)C=2C)C=C4(N3C(C(C)=C4CCC(=O)O)=CC=6(N5C(=C(C)C=6C=C)C=C7C(C=C)=C8C))))))
Download mol2, pdbqt
TPSA 415,12
Non-H Atoms 44
Non-C/H Atoms 10
Metal-Atoms 1
Electronegative Atoms 9
Stereo Centers 0
Rotatable Bonds 8
Rings Closures 8
Small Rings 8
Aromatic Rings 2
Aromatic Atoms 10
sp3-Atoms 13
Symmetric atoms 0
cLogS -11,104
MW 642,041
cLogP 4,3093
HBA 9
HBD 3
Ro5 violations 1
Druglikeness -4,4992
DrugScore 0,121748508341015
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 -3,7984
Caco-2 Permeability 2 0,471
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) 0,8639
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,6722
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6577
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.