| PUBCHEM ID |
57369825
|
| UNII |
5A9BN7V7QL
|
| Preferred Term |
KASUGAMYCIN HYDROCHLORIDE MONOHYDRATE
|
| CAS |
200132-83-8
|
| INCHIKEY |
URDOPMVCASNBEZ-IYWSOWMLSA-N
|
| Download |
mol2, pdbqt
|
| mol2 |
|
| Smiles |
C[C@H]([C@H](C[C@@H]1N)/N=C(/C(O)=O)\N)O[C@@H]1O[C@@H]([C@@H]([C@H]([C@H]([C@@H]1O)O)O)O)[C@H]1O
|
| Total Surface Area |
253,38
|
| Relative PSA |
0,60656
|
| TPSA |
221,31
|
| cLogS |
-0,327
|
| MW |
379,365
|
| cLogP |
-6,7345
|
| H-Acceptors |
12
|
| H-Donors |
8
|
| Ro5 violations |
2
|
| Druglikeness |
-3,704
|
| DrugScore |
0,461134402884757
|
| 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 |
-0,6734
|
| P-glycoprotein Substrate |
Substrate
|
| P-glycoprotein Inhibitor I |
Non-inhibitor
|
| P-glycoprotein Inhibitor II |
Non-inhibitor
|
| Renal Organic Cation Transporter |
Non-inhibitor
|
| Subcellular localization |
Lysosome
|
| CYP450 2C9 Substrate |
Non-substrate
|
| CYP450 2D6 Substrate |
Non-substrate
|
| CYP450 3A4 Substrate |
Non-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 |
Low FHMT
|
| Fish Toxicity II |
1,6011
|
| Tetrahymena Pyriformis Toxicity I |
High TPT
|
| Tetrahymena Pyriformis Toxicity II |
0,3187
|
| Tetrahymena Pyriformis Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
IV
|
| Rat Acute Toxicity |
1,553
|
| Carcinogenicity (Three-class) |
Non-required
|
