Benzo[a]phenazin-5-ol, with the CAS number 2089-82-9, is a polycyclic aromatic compound characterized by its complex fused ring structure, which includes a phenazine core. This compound typically exhibits a dark color and is known for its potential biological activity, including antimicrobial and antitumor properties. The presence of the hydroxyl (-OH) group at the 5-position enhances its reactivity and solubility in polar solvents. Benzo[a]phenazin-5-ol is often studied in the context of organic synthesis and medicinal chemistry due to its structural similarity to other biologically active compounds. Its stability can be influenced by environmental factors such as pH and temperature, and it may undergo various chemical reactions, including oxidation and reduction. Additionally, the compound's interactions with biological systems make it a subject of interest in pharmacological research, particularly in the development of new therapeutic agents. Safety data should be consulted for handling and usage, as with any chemical substance.

Benzo[a]phenazin-5-ol

2089-82-9: Benzo[a]phenazin-5-ol, with the CAS number 2089-82-9, is a polycyclic aromatic compound characterized by its complex fused ring structure, which includes a phenazine core. This compound typically exhibits a dark color and is known for its potential biological activity, including antimicrobial and antitumor properties. The presence of the hydroxyl (-OH) group at the 5-position enhances its reactivity and solubility in polar solvents. Benzo[a]phenazin-5-ol is often studied in the context of organic synthesis and medicinal chemistry due to its structural similarity to other biologically active compounds. Its stability can be influenced by environmental factors such as pH and temperature, and it may undergo various chemical reactions, including oxidation and reduction. Additionally, the compound's interactions with biological systems make it a subject of interest in pharmacological research, particularly in the development of new therapeutic agents. Safety data should be consulted for handling and usage, as with any chemical substance.

sAJM589 is a Myc inhibitor that dose-dependently disrupts Myc-Max heterodimers, thereby decreasing Myc protein levels and inhibiting the cellular proliferation.

sAJM589

<p>sAJM589 is a bifunctional molecule that contains an active methylene group and a photophysical group. In the presence of acid, its fluorescence is enhanced, which may lead to skin cancer. Specifically, sAJM589 has been shown to be cytotoxic in both cancer cells and normal cells. It also induces apoptosis in cancer cells by inhibiting DNA synthesis, protein synthesis, and cell proliferation. The functional theory of this molecule is not yet clear but it may be related to the metal ion binding properties of the molecule.</p>

CAS 2089-82-9

Benzo[a]phenazin-5-ol

sAJM589

Ref: TM-T16839

sAJM589

Ref: 3D-CAA08982