
Common name
imidazol-1-yl-(2,2,4,4-tetramethyl-1,3-oxazolidin-3-yl)methanone
IUPAC name
imidazol-1-yl-(2,2,4,4-tetramethyl-1,3-oxazolidin-3-yl)methanone
SMILES
CC1(N(C(OC1)(C)C)C(=O)N1C=NC=C1)C
Common name
imidazol-1-yl-(2,2,4,4-tetramethyl-1,3-oxazolidin-3-yl)methanone
IUPAC name
imidazol-1-yl-(2,2,4,4-tetramethyl-1,3-oxazolidin-3-yl)methanone
SMILES
CC1(N(C(OC1)(C)C)C(=O)N1C=NC=C1)C
INCHI
InChI=1S/C11H17N3O2/c1-10(2)7-16-11(3,4)14(10)9(15)13-6-5-12-8-13/h5-6,8H,7H2,1-4H3/p+1
FORMULA
C11H17N3O2

Common name
imidazol-1-yl-(2,2,4,4-tetramethyl-1,3-oxazolidin-3-yl)methanone
IUPAC name
imidazol-1-yl-(2,2,4,4-tetramethyl-1,3-oxazolidin-3-yl)methanone
Molecular weight
223.272
clogP
0.557
clogS
-1.345
Frequency
0.0003
HBond Acceptor
3
HBond Donor
0
Total PolarSurface Area
47.36
Number of Rings
2
Rotatable Bond
2
Drug ID | Common name | Structure CAS | Compound class | Therapeutic area |
---|---|---|---|---|
FDBD03045 | oxpoconazole |
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Fungicide | Fungicide |
1 ,
1
FRAGNAME | PDBID | SIMILIRITY | XSCORE | SMILE | HAC |
---|---|---|---|---|---|
1kti_ligand.mol2 | 1kti | 0.393701 | -7.83 | [C@@H]1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)NC(=O)NC(=O)C | 19 |
1k06_ligand.mol2 | 1k06 | 0.393103 | -8.34 | O1[C@H]([C@H](O)[C@@H](O)[C@H](O)[C@H]1CO)NC(=O)NC(=O)c1ccccc1 | 24 |
1k08_ligand.mol2 | 1k08 | 0.393103 | -8.32 | O1[C@H]([C@H](O)[C@@H](O)[C@H](O)[C@H]1CO)NC(=O)NC(=O)c1ccccc1 | 24 |
2prj_ligand.mol2 | 2prj | 0.383333 | -7.51 | [C@@H]1([C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)O)NC(=O)C | 16 |
5d9p_ligand.mol2 | 5d9p | 0.383333 | -6.88 | [C@@H]1([C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)O)NC(=O)C | 16 |
109 ,
11