Molecule Name DB06788
DrugBank Groups Approved
Cluster No 2
Smiles O=C(N1(C(C(O)=NCC)CCC1))C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C2(N=C(O)CC2))CC=3(NC=NC=3))CC=5(C4(=C(C=CC=C4)NC=5)))CO)CC6(=CC=C(O)C=C6))CC=7(N=CN(C=7)CC8(=CC=CC=C8)))CC(C)C)CCCNC(=N)N
Download mol2, pdbqt
TPSA 478,27
Non-H Atoms 96
Non-C/H Atoms 30
Metal-Atoms 0
Electronegative Atoms 30
Stereo Centers 9
Rotatable Bonds 34
Rings Closures 8
Small Rings 8
Aromatic Rings 6
Aromatic Atoms 31
sp3-Atoms 40
Symmetric atoms 5
cLogS -5,585
MW 1323,52
cLogP -0,7553
HBA 30
HBD 16
Ro5 violations 3
Druglikeness 8,0841
DrugScore 0,338875146483949
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 -3,4152
Caco-2 Permeability 2 -0,1509
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) 1,463
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4422
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,7834
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.