| PUBCHEM ID |
91617739
|
| UNII |
1Y1FE6YEU5
|
| Preferred Term |
PHOSPHORAMIDON DISODIUM DIHYDRATE
|
| CAS |
|
| INCHIKEY |
RUUVTTHDXFLIFU-HIKRQZGHSA-L
|
| Download |
mol2, pdbqt
|
| mol2 |
|
| Smiles |
CC(C)C[C@@H](C(N[C@@H](Cc1c[nH]c2c1cccc2)C(O)=O)=O)N[P@](O)(O[C@@H]([C@@H]([C@@H]1O)O)O[C@@H](C)[C@@H]1O)=O
|
| Total Surface Area |
382,17
|
| Relative PSA |
0,43308
|
| TPSA |
220,48
|
| cLogS |
-2,281
|
| MW |
543,508
|
| cLogP |
-2,0425
|
| H-Acceptors |
13
|
| H-Donors |
8
|
| Ro5 violations |
3
|
| Druglikeness |
-25,002
|
| DrugScore |
0,3323333660676
|
| 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 |
-0,7623
|
| P-glycoprotein Substrate |
Substrate
|
| P-glycoprotein Inhibitor I |
Non-inhibitor
|
| P-glycoprotein Inhibitor II |
Non-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 |
1,3872
|
| Tetrahymena Pyriformis Toxicity I |
High TPT
|
| Tetrahymena Pyriformis Toxicity II |
0,5528
|
| Tetrahymena Pyriformis Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity |
2,7483
|
| Carcinogenicity (Three-class) |
Non-required
|
