Molecule Name DB00050
DrugBank Groups Approved
Cluster No 1
Smiles ClC6(=CC=C(CC(NC(=O)C(NC(=O)C)CC2(=CC=1(C(=CC=CC=1)C=C2)))C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N3(C(C(=O)NC(C(=O)N)C)CCC3))CCCNC(=N)N)CC(C)C)CCCNC(=O)N)CC4(=CC=C(O)C=C4))CO)CC5(=CN=CC=C5))C=C6)
Download mol2, pdbqt
TPSA 495,67
Non-H Atoms 102
Non-C/H Atoms 32
Metal-Atoms 0
Electronegative Atoms 32
Stereo Centers 10
Rotatable Bonds 38
Rings Closures 6
Small Rings 6
Aromatic Rings 5
Aromatic Atoms 28
sp3-Atoms 32
Symmetric atoms 5
cLogS -8,313
MW 1431,06
cLogP -0,8875
HBA 31
HBD 17
Ro5 violations 3
Druglikeness 1,0128
DrugScore 0,224000948230682
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 Inhibitor
Renal Organic Cation Transporter Non-inhibitor
Aqueous solubility -3,5765
Caco-2 Permeability 2 -0,1993
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 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) 1,4221
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,5587
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,7014
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.