Pharmaceutical

Salicyloylaminotriazole

  • Chemical Name: Salicyloylaminotriazole
  • CAS: 36411-52-6
  • Purity: 99%
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1.What is the Salicyloylaminotriazole ?

Salicyloylaminotriazole, also known as SCAO or SAT, is a chemical compound with notable biochemical activity. It functions as an inhibitor of isolated protein kinases and has garnered attention in cancer therapy research due to its ability to inhibit the growth of cancer cells. Its lower toxicity compared to other biochemical inhibitors makes it a valuable asset in the field of cancer research. Additionally, Salicyloylaminotriazole is utilized in studying cell differentiation and disease biology, providing valuable insights into the underlying mechanisms of these processes.

2.What is the CAS number for Salicyloylaminotriazole ?

The CAS number of Salicyloylaminotriazole is 36411-52-6.

3.What are another words for Salicyloylaminotriazole ?

Synonyms?for?Salicyloylaminotriazole 36411-52-6:Benzamide,2-hydroxy-N-1H-1,2,4-triazol-3-yl- (9CI); 3-(N-Salicyloyl)amino-1,2,4-triazole;3-(Salicyloylamino)-1,2,4-triazole; 3-Salicylamido-1H-1,2,4-triazole; ADK StabCDA 1; ADK Stab CDA 1M; Adeka CDA 1c; CDA 1; CDA 1M; Mark 1475; Mark CDA 1;Mark CDA 1M; NSC 332171; Salicyloylaminotriazole

4.What is Salicyloylaminotriazole (36411-52-6) used for?

Used in Cancer Therapy Research:
Salicyloylaminotriazole is used as a biochemical inhibitor for [its potential to stop the growth of cancer cells]. It is particularly valuable in this application due to its lower toxicity compared to other inhibitors, making it a favorable contributor in cancer research.
Used in Cell Differentiation Studies:
Salicyloylaminotriazole is used as a research tool for [studying cell differentiation], helping to shed light on the mechanisms behind this biological process.
Used in Disease Biology Research:
Salicyloylaminotriazole is used as a research compound for [studying the biology of diseases], offering insights into the mechanisms that drive various disease processes.

InChI:InChI=1/C9H8N4O2/c14-7-4-2-1-3-6(7)8(15)12-9-10-5-11-13-9/h1-5,14H,(H2,10,11,12,13,15)

Relevant articles related to Salicyloylaminotriazole:

Article

Source

Salicylanilide and its heterocyclic analogues. A comparative study of their antimicrobial activity

Daidone,Maggio,Schillaci

, p. 441 - 442 (2007/10/02)

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