PUBCHEM ID |
2830
|
UNII |
3O1CB88RRD
|
Preferred Term |
COELENTERAZINE
|
CAS |
55779-48-1
|
INCHIKEY |
YHIPILPTUVMWQT-UHFFFAOYSA-N
|
Download |
mol2, pdbqt
|
mol2 |
|
Smiles |
Oc1ccc(CC2=NC3=C(Cc4ccccc4)NC(c(cc4)ccc4O)=CN3C2=O)cc1
|
Total Surface Area |
316,11
|
Relative PSA |
0,20803
|
TPSA |
85,16
|
cLogS |
-5,714
|
MW |
423,471
|
cLogP |
4,0689
|
H-Acceptors |
6
|
H-Donors |
3
|
Ro5 violations |
0
|
Druglikeness |
4,1827
|
DrugScore |
0,485402141415158
|
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 |
0,8242
|
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 |
Non-substrate
|
CYP450 1A2 Inhibitor |
Inhibitor
|
CYP450 2C9 Inhibitor |
Inhibitor
|
CYP450 2D6 Inhibitor |
Non-inhibitor
|
CYP450 2C19 Inhibitor |
Non-inhibitor
|
CYP450 3A4 Inhibitor |
Non-inhibitor
|
CYP Inhibitory Promiscuity |
High 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 |
1,5103
|
Tetrahymena Pyriformis Toxicity I |
High TPT
|
Tetrahymena Pyriformis Toxicity II |
0,3487
|
Tetrahymena Pyriformis Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity |
2,5652
|
Carcinogenicity (Three-class) |
Non-required
|