Molecule Name DB08890
DrugBank Groups Approved
Cluster No 1
Smiles S2(SCC1(NC(=O)C(NC(=O)C(NC(=O)C4(NC(C(CSSCC(NC1=O)C(=O)NC(C(=O)N5(C(C(=O)NC(C(NC(C(NC(C(NCC(NC(C2)C(=O)NC(C(=O)O)CC3(=CC=C(O)C=C3))=O)=O)C(O)C)=O)CSSC4)=O)C)CCC5))CC(=O)N)N)=O))CCC(=O)O)CC6(=CC=C(O)C=C6)))
Download mol2, pdbqt
TPSA 725,71
Non-H Atoms 101
Non-C/H Atoms 42
Metal-Atoms 0
Electronegative Atoms 42
Stereo Centers 14
Rotatable Bonds 13
Rings Closures 6
Small Rings 3
Aromatic Rings 2
Aromatic Atoms 12
sp3-Atoms 43
Symmetric atoms 4
cLogS -5,872
MW 1526,76
cLogP -8,6338
HBA 36
HBD 19
Ro5 violations 3
Druglikeness -6,1793
DrugScore 0,162190059181661
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 -2,8761
Caco-2 Permeability 2 -0,2582
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) 1,4876
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3288
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 3,0981
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.