4702-13-0
4702-13-0
Chemical Structure
N-Phthaloylglycine
Synonym(s): Phthaloyl glycine
- CAS. Nr.: 4702-13-0
- Formula:C10H7NO4
- Molecular Weight:205.17
IUPAC Name: 2-(1,3-dioxoisoindolin-2-yl)acetic acid
InChIKey: WQINSVOOIJDOLJ-UHFFFAOYSA-N
SMILES: C1=CC=CC2=C1C(N(CC(O)=O)C2=O)=O
Biological Activity: N-Phthaloylglycine (Phthaloyl glycine) is a Type II fragmentary hapten (FX-type) with antimicrobial activity. N-Phthaloylglycine acts against Candida albicans, Escherichia coli, and Staphylococcus epidermidis. N-Phthaloylglycine can be used for the research of fungal and bacterial infection[1][2].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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N-Phthaloylglycine | 99.95% | N-Phthaloylglycine (Phthaloyl glycine) is a Type II fragmentary hapten (FX-type) with antimicrobial activity. N-Phthaloylglycine acts against Candida albicans, Escherichia coli, and Staphylococcus epidermidis. N-Phthaloylglycine can be used for the research of fungal and bacterial infection. | ||||||||||||||||||||
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N-Phthaloylglycine-13C2,15N | N-Phthaloylglycine-13C2,15N (Phthaloyl glycine-13C2,15N) is the 13C- and 15N-labeled N-Phthaloylglycine (HY-W014665). N-Phthaloylglycine (Phthaloyl glycine) is an FX-type hapten that attaches to free amine groups of proteins. | |||||||||||||||||||||
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References
- [1]. Mercader JV, et al. Development of monoclonal ELISAs for azinphos-methyl. 1. Hapten synthesis and antibody production. J Agric Food Chem. 1999;47(3):1276-1284. [Content Brief]
- [2]. Alves FS, et al. Antimicrobial Investigation of Phthalimide and N-Phthaloylglycine Esters: Activity, Mechanism of Action, Synergism and Ecotoxicity. Life (Basel). 2025;15(4):518. Published 2025 Mar 21. [Content Brief]
