PUBCHEM ID |
4494
|
UNII |
0214FUT37J
|
Preferred Term |
NILVADIPINE
|
CAS |
75530-68-6
|
INCHIKEY |
|
Download |
mol2, pdbqt
|
mol2 |
|
Smiles |
CC(C)OC(C([C@@H]1c2cc([N@H+]([O-])O)ccc2)=C(C)NC(C#N)=C1C(OC)=O)=O
|
Total Surface Area |
305,29
|
Relative PSA |
0,37613
|
TPSA |
130,16
|
cLogS |
-4,234
|
MW |
387,391
|
cLogP |
1,8883
|
H-Acceptors |
9
|
H-Donors |
3
|
Ro5 violations |
0
|
Druglikeness |
-9,6232
|
DrugScore |
0,369388122672232
|
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 |
1,4626
|
P-glycoprotein Substrate |
Substrate
|
P-glycoprotein Inhibitor I |
Inhibitor
|
P-glycoprotein Inhibitor II |
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 |
Inhibitor
|
CYP450 2C9 Inhibitor |
Inhibitor
|
CYP450 2D6 Inhibitor |
Non-inhibitor
|
CYP450 2C19 Inhibitor |
Inhibitor
|
CYP450 3A4 Inhibitor |
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 |
0,5292
|
Tetrahymena Pyriformis Toxicity I |
High TPT
|
Tetrahymena Pyriformis Toxicity II |
1,2126
|
Tetrahymena Pyriformis Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity |
2,5335
|
Carcinogenicity (Three-class) |
Non-required
|