| PUBCHEM ID |
76968246
|
| UNII |
0AD04KS0VY
|
| Preferred Term |
SCILLIGLAUCOSIDE
|
| CAS |
510-58-7
|
| INCHIKEY |
QDBIBEXZLJNVNH-TVVIPLERSA-N
|
| Download |
mol2, pdbqt
|
| mol2 |
|
| Smiles |
C[C@](CC[C@H]([C@@H]1CC[C@]2(C=CCC3)O[C@H]([C@H]([C@@H]4O)O)O[C@@H](CO)[C@@H]4O)[C@@]23C=O)([C@@H](CC2)C(C=C3)=COC3=O)[C@]12O
|
| Total Surface Area |
386,99
|
| Relative PSA |
0,31417
|
| TPSA |
162,98
|
| cLogS |
-3,891
|
| MW |
560,638
|
| cLogP |
-0,2259
|
| H-Acceptors |
10
|
| H-Donors |
5
|
| Ro5 violations |
1
|
| Druglikeness |
-12,319
|
| DrugScore |
0,28954598437349
|
| 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 |
-0,7552
|
| 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 |
Inhibitor
|
| AMES Toxicity |
Non AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity I |
High FHMT
|
| Fish Toxicity II |
0,9261
|
| Tetrahymena Pyriformis Toxicity I |
High TPT
|
| Tetrahymena Pyriformis Toxicity II |
1,3812
|
| Tetrahymena Pyriformis Toxicity |
High HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
I
|
| Rat Acute Toxicity |
4,4372
|
| Carcinogenicity (Three-class) |
Non-required
|
