Molecule Name DB00512
DrugBank Groups Approved
Cluster No 214
Smiles ClC5(=C6(OC3(=C(OC1(OC(C(O)C(C1OC2(OC(C(O)C(C2)(N)C)C))O)CO))C=4(OC%10(=C(Cl)C=C(C(O)C7(C(=O)NC(C(=O)O)C=9(C(C=8(C=C(C(NC(C(C(=C3)C=4)NC(=O)C(NC(C(C(C(=C5)C=C6)O)NC(=O)C(NC)CC(C)C)=O)CC(=O)N)=O)C(=O)N7)C=CC=8O))=C(O)C=C(O)C=9)))C=C%10)))))
Download mol2, pdbqt
TPSA 530,49
Non-H Atoms 101
Non-C/H Atoms 35
Metal-Atoms 0
Electronegative Atoms 35
Stereo Centers 18
Rotatable Bonds 13
Rings Closures 10
Small Rings 7
Aromatic Rings 5
Aromatic Atoms 30
sp3-Atoms 46
Symmetric atoms 1
cLogS -9,422
MW 1449,27
cLogP -6,7507
HBA 33
HBD 19
Ro5 violations 3
Druglikeness 1,8284
DrugScore 0,235459668207513
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 -3,444
Caco-2 Permeability 2 0,0397
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) 1,2076
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,6265
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,5856
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.