Molecule Name DB04894
DrugBank Groups Approved
Cluster No 854
Smiles S1(SCC(N=C(O)C(N=C(O)C(N=C(C(N=C(C(N=C(C(C1)N=C(O)C(N)CC2(=CC=CC=C2))O)CC3(=CC=C(O)C=C3))O)CC=5(C4(=C(C=CC=C4)NC=5)))O)CCCCN)C(C)C)C(O)=NC(C(O)=N)CC=7(C6(=C(C=CC=C6)NC=7)))
Download mol2, pdbqt
TPSA 426,66
Non-H Atoms 80
Non-C/H Atoms 23
Metal-Atoms 0
Electronegative Atoms 23
Stereo Centers 8
Rotatable Bonds 18
Rings Closures 7
Small Rings 6
Aromatic Rings 6
Aromatic Atoms 30
sp3-Atoms 34
Symmetric atoms 5
cLogS -8,002
MW 1131,39
cLogP 2,2931
HBA 21
HBD 14
Ro5 violations 3
Druglikeness -1,9914
DrugScore 0,142126480648548
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 -3,1004
Caco-2 Permeability 2 -0,4966
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 Inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,4757
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4495
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6221
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.