102494-87-1

Basic information

• Product Name: 2-diaMine
• Synonyms: N1-(2-nitrobenzyl)ethane-1
• CAS NO: 102494-87-1
• Molecular Formula: C₉H₁₃N₃O₂
• Molecular Weight: 195.21842
• Mol File: 102494-87-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-diaMine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-diaMine(102494-87-1)
• EPA Substance Registry System: 2-diaMine(102494-87-1)

Safety Data

• Hazardous Substances Data: 102494-87-1(Hazardous Substances Data)

Upstream product

• 18653-96-8 N,N'-bis(2-nitrobenzylidene)-ethane-1,2-diamine 
• 107-15-3 ethylenediamine 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 1415243-33-2 2,7-bis-[2-(2-nitrobenzylamino)ethyl]benzo[lmn][3,8]phenanthroline-1,3,6,8-tetraone 

Relevant articles and documents

Structure-activity relationships of novel substituted naphthalene diimides as anticancer agents

Novel 1,4,5,8-naphthalenetetracarboxylic diimide (NDI) derivatives were synthesized and evaluated for their antiproliferative activity on a wide number of different tumor cell lines. The prototypes of the present series were derivatives 1 and 2 characterized by interesting biological profiles as anticancer agents. The present investigation expands on the study of structure-activity relationships of prototypes 1 and 2, namely, the influence of the different substituents of the phenyl rings on the biological activity. Derivatives 3-22, characterized by a different substituent on the aromatic rings and/or a different chain length varying from two to three carbon units, were synthesized and evaluated for their cytostatic and cytotoxic activities. The most interesting compound was 20, characterized by a linker of three methylene units and a 2,3,4-trimethoxy substituent on the two aromatic rings. It displayed antiproliferative activity in the submicromolar range, especially against some different cell lines, the ability to inhibit Taq polymerase and telomerase, to trigger caspase activation by a possible oxidative mechanism, to downregulate ERK 2 protein and to inhibit ERKs phosphorylation, without acting directly on microtubules and tubuline. Its theoretical recognition against duplex and quadruplex DNA structures have been compared to experimental thermodynamic measurements and by molecular modeling investigation leading to putative binding modes. Taken together these findings contribute to define this compound as potential Multitarget-Directed Ligands interacting simultaneously with different biological targets.