| Weight | 136.154 g/mol |
|---|---|
| Formula | C7H8N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-AMINOBENZAMIDE (88-68-6)
anthranilamide · ortho-aminobenzamide
Score:
#1051 in Biochemistry
,
#3412 in Chemistry
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- Microanalysis of glycosaminoglycan-derived oligosaccharides labeled with a fluorophore 2-aminobenzamide by high-performance liquid chromatography: application to disaccharide composition analysis and exosequencing of oligosaccharides. (Analytical Biochemistry, 1999)
- Separation of 2-aminobenzamide labeled glycans using hydrophilic interaction chromatography columns packed with 1.7 m sorbent (Journal of Chromatography B, 2010)
- Reversal of P-glycoprotein mediated multidrug resistance by novel anthranilamide derivatives (Bioorganic & Medicinal Chemistry Letters, 1999)
- Anthranilamide and nitrotyrosine as a donor-acceptor pair in internally quenched fluorescent substrates for endopeptidases : multicolumn peptide synthesis of enzyme substrates for subtilisin Carlsberg and pepsin (Analytical Biochemistry, 1991)
- Discovery of novel 2-aminobenzamide inhibitors of heat shock protein 90 as potent, selective and orally active antitumor agents. (Journal of Medicinal Chemistry, 2009)
- Recovery of intact 2-aminobenzamide-labeled O-glycans released from glycoproteins by hydrazinolysis. (Analytical Biochemistry, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - anthranilamide
- ortho-aminobenzamide
-
SMILESC1=CC=C(C(=C1)C(=O)N)N
-
InChIKeyPXBFMLJZNCDSMP-UHFFFAOYSA-N
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2-AMINOBENZAMIDE
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