Molecule Name DB02903
DrugBank Groups Experimental
Cluster No 637
Smiles O=[N+]([O-])C2(=CC(OC1(OC(C(O)C(C1O)O)CO))=CC(=C2)C(O)=NCCCN8(CCN(CCCNC7(=C(NCCN=C(OCC(N)COC(O)=NCCNC6(=C(NCCCN5(CCN(CCCN=C(O)C4(=CC(OC3(OC(C(O)C(C3O)O)CO))=CC(=C4)[N+](=O)[O-]))CC5))C(=O)C6=O))O)C(=O)C7=O))CC8))
Download mol2, pdbqt
TPSA 1062,6
Non-H Atoms 104
Non-C/H Atoms 41
Metal-Atoms 0
Electronegative Atoms 41
Stereo Centers 11
Rotatable Bonds 42
Rings Closures 8
Small Rings 8
Aromatic Rings 2
Aromatic Atoms 12
sp3-Atoms 64
Symmetric atoms 4
cLogS -3,285
MW 1474,49
cLogP -12,59
HBA 41
HBD 17
Ro5 violations 3
Druglikeness -4,1459
DrugScore 0,234535971706593
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 Inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,0925
Caco-2 Permeability 2 -0,0404
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 Strong inhibitor
Human Ether-a-go-go-Related Gene Inhibition 2 Inhibitor
AMES Toxicity AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,3816
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5613
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6012
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.