Molecule Name DB00403
DrugBank Groups Approved
Cluster No 3
Smiles S(=O)(=O)(OC5(=CC=C(CC(NC(=O)C(NC(=O)C(NC(=O)C1(NC(=O)CC1))CCC(=O)N)CC(=O)O)C(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N)CC2(=CC=CC=C2))CC(=O)O)CCSC)CC=4(C3(=C(C=CC=C3)NC=4)))C(O)C)C=C5))O
Download mol2, pdbqt
TPSA 585,08
Non-H Atoms 94
Non-C/H Atoms 36
Metal-Atoms 0
Electronegative Atoms 36
Stereo Centers 10
Rotatable Bonds 38
Rings Closures 5
Small Rings 5
Aromatic Rings 4
Aromatic Atoms 21
sp3-Atoms 31
Symmetric atoms 5
cLogS -4,748
MW 1352,42
cLogP -6,8549
HBA 34
HBD 17
Ro5 violations 3
Druglikeness 7,6725
DrugScore 0,390589006253599
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 -3,3567
Caco-2 Permeability 2 -0,4619
Subcellular localization Lysosome
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) 1,4692
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,4193
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6037
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.