| PUBCHEM ID |
91827079
|
| UNII |
2QA8975A8D
|
| Preferred Term |
2H-FURO(3,2-B)PYRAN-2-ONE, HEXAHYDRO-7A-METHYL-5-(1-METHYLETHENYL)-, (3AR,5R,7AR)-
|
| CAS |
1640022-48-5
|
| INCHIKEY |
AWABGJZCNJGFRA-IWSPIJDZSA-N
|
| Download |
mol2, pdbqt
|
| mol2 |
|
| Smiles |
CC([C@H](CC1)O[C@@H](C2)[C@H]1OC2=O)=C
|
| Total Surface Area |
138,04
|
| Relative PSA |
0,23935
|
| TPSA |
35,53
|
| cLogS |
-2,177
|
| MW |
182,218
|
| cLogP |
1,056
|
| H-Acceptors |
3
|
| H-Donors |
0
|
| Ro5 violations |
0
|
| Druglikeness |
-17,498
|
| DrugScore |
0,4761612882034
|
| 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 |
0,9246
|
| P-glycoprotein Substrate |
Substrate
|
| P-glycoprotein Inhibitor I |
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 |
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 |
0,6342
|
| Tetrahymena Pyriformis Toxicity I |
Low TPT
|
| Tetrahymena Pyriformis Toxicity II |
-0,1394
|
| Tetrahymena Pyriformis Toxicity |
High HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity |
2,1156
|
| Carcinogenicity (Three-class) |
Non-required
|
