| PUBCHEM ID |
86346053
|
| UNII |
HDN0B924X4
|
| Preferred Term |
LEFAMULIN ACETATE
|
| CAS |
1350636-82-6
|
| INCHIKEY |
WSMXIQXWHPSVDE-ZPJPNJFZSA-N
|
| Download |
mol2, pdbqt
|
| mol2 |
|
| Smiles |
C[C@@H](CC[C@](CC1)([C@@H]2C1=O)[C@H](C)[C@H]([C@](C)(C1)C=C)O)[C@]2(C)[C@H]1OC(CS[C@@H](CC[C@@H](C1)N)[C@H]1O)=O
|
| Total Surface Area |
372,36
|
| Relative PSA |
0,25524
|
| TPSA |
135,15
|
| cLogS |
-5,343
|
| MW |
507,733
|
| cLogP |
3,8144
|
| H-Acceptors |
6
|
| H-Donors |
3
|
| Ro5 violations |
1
|
| Druglikeness |
-0,71163
|
| DrugScore |
0,306598736390506
|
| Mutagenic |
none
|
| Tumorigenic |
none
|
| Reproductive Effective |
none
|
| Irritant |
none
|
| Blood-Brain Barrier |
BBB+
|
| Human Intestinal Absorption |
HIA+
|
| Caco-2 Permeability I |
Caco2-
|
| Caco-2 Permeability II |
0,2836
|
| P-glycoprotein Substrate |
Substrate
|
| P-glycoprotein Inhibitor I |
Non-inhibitor
|
| P-glycoprotein Inhibitor II |
Inhibitor
|
| Renal Organic Cation Transporter |
Non-inhibitor
|
| 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 I |
Weak inhibitor
|
| Human Ether-a-go-go-Related Gene Inhibition II |
Non-inhibitor
|
| AMES Toxicity |
Non AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity I |
High FHMT
|
| Fish Toxicity II |
0,9311
|
| Tetrahymena Pyriformis Toxicity I |
High TPT
|
| Tetrahymena Pyriformis Toxicity II |
0,8111
|
| Tetrahymena Pyriformis Toxicity |
High HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity |
2,6815
|
| Carcinogenicity (Three-class) |
Non-required
|
