Molecule Name DB02792
DrugBank Groups Experimental
Cluster No 741
Smiles ClC4(=C5(OC2(=C(O)C=3(OC9(=C(Cl)C=C(C(OC1(OC(C(O)(O)C(C1)(N)C)C))C6(C(O)=NC(C(=O)O)C=8(C(C=7(C=C(C(N=C(C(C(=C2)C=3)N=C(O)C(N=C(C(C(C(=C4)C=C5)O)N=C(O)C(NC)CC(C)C)O)CC(O)=N)O)C(O)=N6)C=CC=7O))=C(O)C=C(O)C=8)))C=C9)))))
Download mol2, pdbqt
TPSA 893,65
Non-H Atoms 91
Non-C/H Atoms 31
Metal-Atoms 0
Electronegative Atoms 31
Stereo Centers 12
Rotatable Bonds 10
Rings Closures 9
Small Rings 6
Aromatic Rings 5
Aromatic Atoms 30
sp3-Atoms 43
Symmetric atoms 2
cLogS -8,707
MW 1303,13
cLogP -4,1373
HBA 29
HBD 18
Ro5 violations 3
Druglikeness 5,7535
DrugScore 0,204471151977011
Mutagenic none
Tumorigenic none
Reproductive Effective low
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 -3,457
Caco-2 Permeability 2 -0,3076
Subcellular localization Lysosome
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) 1,1443
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,6977
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,7023
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.