structure of 2-BenzothiazolaMine, 5,7-dibroMo-

2-BenzothiazolaMine, 5,7-dibroMo-

CAS No.: 1000289-40-6
M. Wt: 307.99300
M. Fa: C7H4Br2N2S
InChI Key: -

Names and Identifiers of 2-BenzothiazolaMine, 5,7-dibroMo-

CAS Number

1000289-40-6

IUPAC Name

5,7-bis(bromanyl)-1,3-benzothiazol-2-amine

Canonical SMILES

C1=C(C=C(C2=C1N=C(S2)N)Br)Br

Physical and chemical properties of 2-BenzothiazolaMine, 5,7-dibroMo-

Exact Mass

305.84600

LogP

3.33360

Molecular Formula

C7H4Br2N2S

Molecular Weight

307.99300

PSA

67.88000

Applications of 2-BenzothiazolaMine, 5,7-dibroMo-

2-Amino-5,7-dibromobenzothiazole serves multiple purposes across various fields:

  • Pharmaceuticals: Due to its biological activities, it is explored as a potential lead compound for developing new drugs targeting cancer and infectious diseases.
  • Materials Science: Its unique structural properties make it suitable for creating advanced materials with specific electronic or optical characteristics.
  • Agriculture: There is potential for developing agrochemicals based on its antimicrobial properties.

Interaction Studies of 2-BenzothiazolaMine, 5,7-dibroMo-

Studies on the interactions of 2-Amino-5,7-dibromobenzothiazole with biological systems reveal its potential effects on enzyme activity and cellular processes. For example, its interaction with cytochrome P450 enzymes may alter drug metabolism pathways, suggesting implications for pharmacokinetics and drug-drug interactions. Additionally, research into its cytotoxic effects on cancer cells indicates that it may induce apoptosis through oxidative stress mechanisms.

Biological Activity of 2-BenzothiazolaMine, 5,7-dibroMo-

2-Amino-5,7-dibromobenzothiazole exhibits a range of biological activities attributed to its thiazole core. Research indicates that thiazole derivatives can possess antioxidant, antimicrobial, antifungal, antiviral, anti-inflammatory, and anticancer properties. The compound's interaction with cytochrome P450 enzymes suggests that it may influence drug metabolism and cellular signaling pathways. Additionally, its ability to generate reactive oxygen species could contribute to its cytotoxic effects against certain cancer cell lines.