| PUBCHEM ID |
91618088
|
| UNII |
60202OBY3A
|
| Preferred Term |
CITRIFOLINOSIDE A
|
| CAS |
350590-52-2
|
| INCHIKEY |
PPNNIWJAKIMLID-HJZUTWSRSA-N
|
| Download |
mol2, pdbqt
|
| mol2 |
|
| Smiles |
COC(C([C@H]([C@H]1O[C@@H]11)[C@@H]2[C@@]1([C@H](/C1=C\c(cc3)ccc3O)O)O/C1=O)=CO[C@@H]2O[C@H]([C@H]([C@@H]1O)O)O[C@@H](CO)[C@@H]1O)=O
|
| Total Surface Area |
370,36
|
| Relative PSA |
0,4653
|
| TPSA |
214,2
|
| cLogS |
-1,99
|
| MW |
564,494
|
| cLogP |
-2,705
|
| H-Acceptors |
14
|
| H-Donors |
6
|
| Ro5 violations |
3
|
| Druglikeness |
-5,1358
|
| DrugScore |
0,116275534482293
|
| Mutagenic |
none
|
| Tumorigenic |
high
|
| Reproductive Effective |
high
|
| Irritant |
none
|
| Blood-Brain Barrier |
BBB-
|
| Human Intestinal Absorption |
HIA+
|
| Caco-2 Permeability I |
Caco2-
|
| Caco-2 Permeability II |
-0,4442
|
| 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 |
AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity I |
High FHMT
|
| Fish Toxicity II |
0,1321
|
| Tetrahymena Pyriformis Toxicity I |
High TPT
|
| Tetrahymena Pyriformis Toxicity II |
0,6104
|
| Tetrahymena Pyriformis Toxicity |
High HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity |
3,4403
|
| Carcinogenicity (Three-class) |
Non-required
|
