92-82-0
92-82-0
Chemical Structure
Phenazine
- CAS No.: 92-82-0
- Formula:C12H8N2
- Molecular Weight:180.21
IUPAC Name: phenazine
InChIKey: PCNDJXKNXGMECE-UHFFFAOYSA-N
SMILES: C12=NC3=CC=CC=C3N=C1C=CC=C2
Biological Activity: Phenazine belongs to the family of N-heterocyclic compounds. Phenazine can be found in terrestrial and marine microorganisms. Phenazine attracts attention due to its diverse biological activities, including Antimicrobial and enzyme inhibitory properties. Phenazine can be used in breast cancer research[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Phenazine | 99.94% | Phenazine belongs to the family of N-heterocyclic compounds. Phenazine can be found in terrestrial and marine microorganisms. Phenazine attracts attention due to its diverse biological activities, including Antimicrobial and enzyme inhibitory properties. Phenazine can be used in breast cancer research. | ||||||||||||||||||||
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Phenazine (Standard) | ≥98% | Phenazine (Standard) is the analytical standard of Phenazine (HY-W016477). This product is intended for research and analytical applications. Phenazine belongs to the family of N-heterocyclic compounds. Phenazine can be found in terrestrial and marine microorganisms. Phenazine attracts attention due to its diverse biological activities, including Antimicrobial and enzyme inhibitory properties. Phenazine can be used in breast cancer research. | ||||||||||||||||||||
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1-Aminoacridine | 1-Aminoacridine (1-Acridinamine) is a bright fluorescent dye. 1-Aminoacridine acts as an anti-infective agent and mutagen due to its ability to interact with DNA. | |||||||||||||||||||||
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Phenazine oxide | 99.45% | Phenazine oxide (Phenazine N-oxide) is a novel and potent fungicide, bactericide, and wood preservative. | ||||||||||||||||||||
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6-Aminophenanthridine | 6-Aminophenanthridine inhibits the protein folding activity of the ribosome (PFAR). 6-Aminophenanthridine competitively occludes the protein substrates from binding to rRNA and thereby inhibits PFAR. | |||||||||||||||||||||
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2,3-Dihydroxyquinoxaline | 2,3-Dihydroxyquinoxaline is a fluorescent reagent. 2,3-Dihydroxyquinoxaline can be used for the determination of trace Pb(II) in vinegar. | |||||||||||||||||||||
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9-Aminoacridine (Standard) | ≥98% | 9-Aminoacridine (Standard) is the analytical standard of 9-Aminoacridine. This product is intended for research and analytical applications. 9-Aminoacridine, a fluorescent probe, acts as an indicator of pH for quantitative determination of transmembrane pH gradients (inside acidic). 9-Aminoacridine is an antimicrobial. 9-Aminoacridine exerts its antimicrobial activity by interacting with specific bacterial DNA and disrupting the proton motive force in K. pneumoniae. 9-Aminoacridine is a HIV-1 inhibitor and inhibits HIV LTR transcription highly dependent on the presence and location of the amino moiety. 9-Aminoacridine inhibits virus replication in HIV-1 infected cell lines. 9-Aminoacridine is used as a Rifampin (RIF; HY-B0272) adjuvant for the multidrug-resistant K. pneumoniae infections. | ||||||||||||||||||||
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Carbamazepine impurity 7 | Carbamazepine impurity 7 is an impurity of Carbamazepine. | |||||||||||||||||||||
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2-Methylquinoxaline | 2-Methylquinoxaline is a detection marker of Methylglyoxal (HY-106634) and can be used for quantitative Methylglyoxal. 2-Methylquinoxaline can be used for the researches of type 2 diabetes and Alzheimer's disease. | |||||||||||||||||||||
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1-Hydroxyphenazine | 99.80% | 1-Hydroxyphenazine (Hemipyocyanine; 1-Phenazinol; Hemi-pyocyanin) is an inhibitor for α-Amylase with an IC50 of 3.1 μg/mL. 1-Hydroxyphenazine exhibits anticancer and anti-inflammatory activity against cells A549, 1321N1 and RAW264.7, antifungal and antibacterial activity against strains Candida albicans, Aspergillus fumigatus, Escherichia coli and Xanthomonas campestris. | ||||||||||||||||||||
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Phenanthridine | Phenanthridine is an aldehyde oxidase 1 (AOX1) substrate, with oxidation by hAOX1 yielding phenanthridone when molecular oxygen, ferricyanide, or dichlorophenolindophenol serves as electron acceptor. | |||||||||||||||||||||
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References
- [1]. Khalili N S D. Synthesis, Biological Activity And Molecular Docking Of Imidazole-Phenazine Derivatives As Potential Inhibitors For Ns2b-Ns3 Dengue Protease[D]., 2024.
- [2]. Yang Y, et al. Phenazine derivatives attenuate the stemness of breast cancer cells through triggering ferroptosis. Cellular and molecular life sciences : CMLS. 2022 Jun 11;79(7):360. [Content Brief]
