| PUBCHEM ID |
91810597
|
| UNII |
9548016401
|
| Preferred Term |
DIHYDROXYHOMOTYROSINE, (S,S,S)-
|
| CAS |
106454-67-5
|
| INCHIKEY |
SKALBOHJGVPGFQ-CIUDSAMLSA-N
|
| Download |
mol2, pdbqt
|
| mol2 |
|
| Smiles |
N[C@H]([C@H]([C@@H](c(cc1)ccc1O)O)O)C(O)=O
|
| Total Surface Area |
162,43
|
| Relative PSA |
0,49689
|
| TPSA |
124,01
|
| cLogS |
-0,568
|
| MW |
227,215
|
| cLogP |
-3,5324
|
| H-Acceptors |
6
|
| H-Donors |
5
|
| Ro5 violations |
0
|
| Druglikeness |
-5,3123
|
| DrugScore |
0,49033825800839
|
| 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 |
-0,2631
|
| P-glycoprotein Substrate |
Non-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 |
High FHMT
|
| Fish Toxicity II |
1,825
|
| Tetrahymena Pyriformis Toxicity I |
High TPT
|
| Tetrahymena Pyriformis Toxicity II |
-0,8809
|
| Tetrahymena Pyriformis Toxicity |
Low HBT
|
| Biodegradation |
Ready biodegradable
|
| Acute Oral Toxicity |
IV
|
| Rat Acute Toxicity |
1,4943
|
| Carcinogenicity (Three-class) |
Non-required
|
