| Smiles |
S1(SCC(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C5(NC(=O)C(NC(=O)CNC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(C1)NC(=O)C(NC(=O)C(NC(=O)C(N)CCCNC(=N)N)CCCNC(=N)N)CC=3(C2(=C(C=CC=C2)NC=3)))=O)CC4(=CC=C(O)C=C4))=O)CCCNC(=N)N)=O)CCCCN)=O)CSSC5)=O)CC6(=CC=C(O)C=C6))=O)CCCCN)=O)CC
|
| CAS number |
147658-54-6
|
| Polar Surface Area |
1149,3
|
| calculated LogS |
-9,172
|
| Molweight |
2487,01
|
| calculated LogP |
-9,7844
|
| H-Acceptors |
60
|
| H-Donors |
42
|
| Ro5 violations |
3
|
| Druglikeness |
1,2714
|
| DrugScore |
0,2260038
|
| Mutagenic |
none
|
| Tumorigenic |
none
|
| Reproductive Effective |
none
|
| Irritant |
none
|
| Fish Toxicity |
High FHMT
|
| Fish Toxicity2 |
1,5278
|
| Rat Acute Toxicity |
2,578
|
| Acute Oral Toxicity |
III
|
| Caco-2 Permeability |
Caco2-
|
| Caco-2 Permeability2 |
-0,7074
|
| P-glycoprotein Substrate |
Substrate
|
| P-glycoprotein Inhibitor |
Non-inhibitor
|
| P-glycoprotein Inhibitor2 |
Non-inhibitor
|
| Human Ether-a-go-go-Related Gene Inhibition |
Weak inhibitor
|
| Human Ether-a-go-go-Related Gene Inhibition2 |
Inhibitor
|
| CYP450 2C9 Substrate |
Non-substrate
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity2 |
0,3691
|
| AMES Toxicity |
Non AMES toxic
|
| CYP450 3A4 Substrate |
Non-substrate
|
| CYP450 3A4 Inhibitor |
Non-inhibitor
|
| CYP450 2C19 Inhibitor |
Non-inhibitor
|
| CYP450 2C9 Inhibitor |
Non-inhibitor
|
| CYP450 2D6 Inhibitor |
Non-inhibitor
|
| CYP450 1A2 Inhibitor |
Non-inhibitor
|
| CYP450 2D6 Substrate |
Non-substrate
|
| Biodegradation |
Not ready biodegradable
|
| Carcinogens |
Non-carcinogens
|
| Blood-Brain Barrier |
BBB-
|
| CYP Inhibitory Promiscuity |
Low CYP Inhibitory Promiscuity
|
| Honey Bee Toxicity |
Low HBT
|
| Renal Organic Cation Transporter |
Non-inhibitor
|
| Carcinogenicity (Three-class) |
Non-required
|
| Human Intestinal Absorption |
HIA+
|
| Structure |
147658-54-6
|
