| PUBCHEM ID |
90479312
|
| UNII |
288OER048N
|
| Preferred Term |
ESTRADIOL 17-P-PROPOXYPHENYL PROPIONATE
|
| CAS |
7724-88-1
|
| INCHIKEY |
JNWIUSBBFNMZRQ-BOJCFLQHSA-N
|
| Download |
mol2, pdbqt
|
| mol2 |
|
| Smiles |
CCCOc1ccc(CCC(O[C@@H](CC2)[C@@](C)(CC3)[C@@H]2[C@H](CC2)[C@H]3c(cc3)c2cc3O)=O)cc1
|
| Total Surface Area |
359,15
|
| Relative PSA |
0,12847
|
| TPSA |
55,76
|
| cLogS |
-6,423
|
| MW |
462,628
|
| cLogP |
7,0482
|
| H-Acceptors |
4
|
| H-Donors |
1
|
| Ro5 violations |
1
|
| Druglikeness |
-3,3571
|
| DrugScore |
8,30540497507749E-02
|
| Mutagenic |
none
|
| Tumorigenic |
none
|
| Reproductive Effective |
high
|
| Irritant |
none
|
| Blood-Brain Barrier |
BBB+
|
| Human Intestinal Absorption |
HIA+
|
| Caco-2 Permeability I |
Caco2+
|
| Caco-2 Permeability II |
0,9686
|
| 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 |
-0,3103
|
| Tetrahymena Pyriformis Toxicity I |
High TPT
|
| Tetrahymena Pyriformis Toxicity II |
2,2327
|
| Tetrahymena Pyriformis Toxicity |
High HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity |
2,075
|
| Carcinogenicity (Three-class) |
Non-required
|
