655-86-7
655-86-7
Chemical Structure
2,3-Diaminophenazine
Synonym(s): 2,3-Phenazinediamine; NNC39-0028
- CAS. Nr.: 655-86-7
- Formula:C12H10N4
- Molecular Weight:210.24
IUPAC Name: phenazine-2,3-diamine
InChIKey: VZPGINJWPPHRLS-UHFFFAOYSA-N
SMILES: NC1=CC2=NC3=CC=CC=C3N=C2C=C1N
Biological Activity: 2,3-Diaminophenazine (2,3-Phenazinediamine) is an orally active amino derivative of phenazine. 2,3-Diaminophenazine can intercalate into DNA. 2,3-Diaminophenazine triggers photochemical reactions. 2,3-Diaminophenazine inhibits vascular hypertrophy and tissue AGE deposition in diabetic rats. 2,3-Diaminophenazine can be used for luminescence and diabetes research[1][2][3][4].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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2,3-Diaminophenazine | 99.84% | 2,3-Diaminophenazine (2,3-Phenazinediamine) is an orally active amino derivative of phenazine. 2,3-Diaminophenazine can intercalate into DNA. 2,3-Diaminophenazine triggers photochemical reactions. 2,3-Diaminophenazine inhibits vascular hypertrophy and tissue AGE deposition in diabetic rats. 2,3-Diaminophenazine can be used for luminescence and diabetes research. | ||||||||||||||||||||
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References
- [1]. Xiaoyue He, et al. Selective self-assembly of 2,3-diaminophenazine molecules on MoSe 2 mirror twin boundaries. Nat Commun. 2019 Jun 28;10(1):2847. [Content Brief]
- [2]. Feng Zhang, et al. An enzymatic ratiometric fluorescence assay for 6-mercaptopurine by using MoS 2 quantum dots. Mikrochim Acta. 2018 Nov 10;185(12):540. [Content Brief]
- [3]. Fu PK, et al. Photoinduced DNA cleavage and cellular damage in human dermal fibroblasts by 2,3-diaminophenazine. Photochem Photobiol. 2005 Jan-Feb;81(1):89-95. [Content Brief]
- [4]. Soulis T, et al. A novel inhibitor of advanced glycation end-product formation inhibits mesenteric vascular hypertrophy in experimental diabetes. Diabetologia. 1999 Apr;42(4):472-9. [Content Brief]
