Molecule Name DB00014
DrugBank Groups Approved
Cluster No 2
Smiles O=C6(NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1(C(C(=O)NNC(=O)N)CCC1))CCCN=C(N)N)CC(C)C)COC(C)(C)C)CC2(=CC=C(O)C=C2))CO)CC=4(C3(=C(C=CC=C3)NC=4)))CC=5(NC=NC=5))CC6)
Download mol2, pdbqt
TPSA 495,89
Non-H Atoms 91
Non-C/H Atoms 32
Metal-Atoms 0
Electronegative Atoms 32
Stereo Centers 9
Rotatable Bonds 33
Rings Closures 6
Small Rings 6
Aromatic Rings 4
Aromatic Atoms 20
sp3-Atoms 33
Symmetric atoms 6
cLogS -6,432
MW 1269,43
cLogP -4,3218
HBA 32
HBD 17
Ro5 violations 3
Druglikeness -1,4466
DrugScore 0,17751484356634
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 -3,5839
Caco-2 Permeability 2 -0,3648
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) 1,3639
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5164
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,673
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.