
Common name
2-hydroxy-N-methyl-acetamide
IUPAC name
2-hydroxy-N-methyl-acetamide
SMILES
C(O)C(=O)NC
Common name
2-hydroxy-N-methyl-acetamide
IUPAC name
2-hydroxy-N-methyl-acetamide
SMILES
C(O)C(=O)NC
INCHI
InChI=1S/C3H7NO2/c1-4-3(6)2-5/h5H,2H2,1H3,(H,4,6)
FORMULA
C3H7NO2

Common name
2-hydroxy-N-methyl-acetamide
IUPAC name
2-hydroxy-N-methyl-acetamide
Molecular weight
89.093
clogP
-0.803
clogS
0.002
Frequency
0.0017
HBond Acceptor
2
HBond Donor
2
Total PolarSurface Area
49.33
Number of Rings
0
Rotatable Bond
1
Drug ID | Common name | Structure CAS | Compound class | Therapeutic area |
---|---|---|---|---|
FDBD01251 | Lopinavir |
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Anti-HIV Agents; HIV Protease Inhibitors; Antiinfectives for Systemic Use; Direct Acting Antivirals; Antivirals for Systemic Use; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP2C9 Inhibitors; Cytochrome P-450 CYP1A2 Inducers; Cytochrome P-450 CYP3A Inhibitors; Cytochrome P-450 CYP2C9 Inducers; Cytochrome P-450 CYP2C19 Inducers; Cytochrome P-450 CYP2B6 Inducers; Cytochrome P-450 CYP2B6 Inhibitors; CYP2B6 Inhibitors (strong); CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP3A4 Inhibitors; Combined Inhibitors of CYP3A4 and P-glycoprotein; | Indicated in combination with other antiretroviral agents for the treatment of HIV-infection. |
FDBD01703 | Ioversol |
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Contrast Media; X-Ray Contrast Media, Iodinated; Watersoluble, Nephrotropic, Low Osmolar X-Ray Contrast Media; | |
FDBD02353 | beflubutamid |
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Herbicide | Herbicide |
FDBD02393 | mefenacet |
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Herbicide | Herbicide |
FDBD02911 | mandipropamid |
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Fungicide | Fungicide |
5 ,
1
FRAGNAME | PDBID | SIMILIRITY | XSCORE | SMILE | HAC |
---|---|---|---|---|---|
4q4i_ligand_2_30.mol2 | 4q4i | 1 | -5.82 | C(O)C(=O)NC | 6 |
4kx8_ligand_2_30.mol2 | 4kx8 | 1 | -5.68 | C(O)C(=O)NC | 6 |
4wk7_ligand_3_6.mol2 | 4wk7 | 1 | -5.59 | CNC(=O)CO | 6 |
1mjj_ligand_3_121.mol2 | 1mjj | 1 | -5.58 | C(O)C(=O)NC | 6 |
1bsk_ligand_3_48.mol2 | 1bsk | 1 | -5.52 | CNC(=O)CO | 6 |
1mh5_ligand_3_121.mol2 | 1mh5 | 1 | -5.52 | OCC(=O)NC | 6 |
142 ,
15