550-89-0
550-89-0
Chemical Structure
Oxychlororaphine
- CAS No.: 550-89-0
- Formula:C13H9N3O
- Molecular Weight:223.23
IUPAC Name: phenazine-1-carboxamide
InChIKey: KPZYYKDXZKFBQU-UHFFFAOYSA-N
SMILES: O=C(C1=CC=CC2=NC3=CC=CC=C3N=C21)N
Biological Activity: Oxychloroaphine could be isolated from the bacterium Pantoea agglomerans naturally present in soil. Oxychloroaphine has broad-spectrum antifungal activity. Oxychloroaphine has cytotoxicity in a dose-dependent manner and induces apoptosis. Oxychloroaphine can be used in research of cancer[1][2].
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Oxychlororaphine | 98.63% | Oxychloroaphine could be isolated from the bacterium Pantoea agglomerans naturally present in soil. Oxychloroaphine has broad-spectrum antifungal activity. Oxychloroaphine has cytotoxicity in a dose-dependent manner and induces apoptosis. Oxychloroaphine can be used in research of cancer. | ||||||||||||||||||||
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Oxychlororaphine (Standard) | ≥98% | Oxychlororaphine (Standard) is the analytical standard of Oxychlororaphine. This product is intended for research and analytical applications. Oxychloroaphine could be isolated from the bacterium Pantoea agglomerans naturally present in soil. Oxychloroaphine has broad-spectrum antifungal activity. Oxychloroaphine has cytotoxicity in a dose-dependent manner and induces apoptosis. Oxychloroaphine can be used in research of cancer. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.86
HY-33037RPhenazine-1-carboxylic acid (Standard) -
Similarity Score 0.71
HY-W129730Phenazine-1,6-dicarboxylic acid -
Similarity Score 0.69
HY-N14686Phencomycin -
Similarity Score 0.66
HY-W780198Endophenazine A -
Similarity Score 0.66
HY-14206NU 1085 -
Similarity Score 0.66
HY-W103062R9-Acridinecarboxylic acid monohydrate (Standard) -
Similarity Score 0.66
HY-W0227599-Acridinecarboxylic acid -
Similarity Score 0.66
HY-W0200862,3-Diaminophenazine -
Similarity Score 0.66
HY-W026644Acridine-9-carboxaldehyde -
Explore the MedChemAI to find more analogs
References
- [1]. Li S, et, al. Comparative metabolomics and transcriptomics analyses provide insights into the high-yield mechanism of phenazines biosynthesis in Pseudomonas chlororaphis GP72. J Appl Microbiol. 2022 Nov;133(5):2790-2801. [Content Brief]
- [2]. Ali HM, et, al. Isolation of Bioactive Phenazine-1-Carboxamide from the Soil Bacterium Pantoea agglomerans and Study of Its Anticancer Potency on Different Cancer Cell Lines. J AOAC Int. 2016 Sep;99(5):1233-9. [Content Brief]
