| PUBCHEM ID |
86278165
|
| UNII |
6897GXD6OE
|
| Preferred Term |
FERRIC CARBOXYMALTOSE
|
| CAS |
9007-72-1
|
| INCHIKEY |
|
| Download |
mol2, pdbqt
|
| mol2 |
|
| Smiles |
OC[C@H]([C@@H]([C@H]([C@@H](C(O)=O)O)O)O[C@H]([C@@H]([C@H]1O)O)O[C@H](CO)[C@H]1O[C@H]([C@@H]([C@H]1O)O)O[C@H](CO)[C@H]1O[C@H]([C@@H]([C@H]1O)O)O[C@H](CO)[C@H]1O)O
|
| Total Surface Area |
438,54
|
| Relative PSA |
0,61463
|
| TPSA |
375,9
|
| cLogS |
1,464
|
| MW |
682,575
|
| cLogP |
-9,0067
|
| H-Acceptors |
22
|
| H-Donors |
15
|
| Ro5 violations |
3
|
| Druglikeness |
-9,4714
|
| DrugScore |
0,274949642875599
|
| 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 |
-0,6878
|
| 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 |
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 |
2,1539
|
| Tetrahymena Pyriformis Toxicity I |
High TPT
|
| Tetrahymena Pyriformis Toxicity II |
-0,1449
|
| Tetrahymena Pyriformis Toxicity |
High HBT
|
| Biodegradation |
Ready biodegradable
|
| Acute Oral Toxicity |
IV
|
| Rat Acute Toxicity |
1,3085
|
| Carcinogenicity (Three-class) |
Non-required
|
