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Tyrphostin 51

Drug details:
Molecular formula: C13H8N4O3

Classification: Benzenetriols and derivatives; Phenols; Benzenoids; Organic compounds;
Synonyms:  2-Amino-1,1,3-tricyano-4-(3',4',5'-trihydroxyphenyl)butadiene
(3Z)-2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile
1,3-Butadiene-1,1,3-tricarbonitrile, 2-amino-4-(3,4,5-trihydroxyphenyl)-
(Z)-2-amino-4-(3,4,5-trihydroxyphenyl)buta-1,3-diene-1,1,3-tricarbonitrile
3-Amino-2,4-dicyano-5-(3',4',5'-trihydroxyphenyl)penta-2,4-dienonitrile
2-Amino-1,1,3-tricyano-4-[3',4',5'-trihydroxyphenyl]butadiene
Tyrphostin 51, >=98%
2-amino-4-(3,4,5-trihydroxyphenyl)-1,3-butadiene-1,1,3-tricarbonitrile
1,3-Butadiene-1,1,3-tricarbonitrile, 2-amino-4-(3,4,5-trihydroxyphenyl)-, (Z)-

Chemical structure:
Depiction based on curated SMILES NH 2 N N N OH OH OH

Francisella
Related VF: Acid phosphatase
Target: AcpA
Drug effect: Inhibits a secreted alkaline phosphatase AcpA activity to reduce intracellular burden of F. tularensis.
Max phase: In vitro
Publication:
Fernández-Soto P, et al., 2021. Discovery of uncompetitive inhibitors of SapM that compromise intracellular survival of Mycobacterium tuberculosis. Sci Rep 11(1):7667.

Mycobacterium
Related VFcategory: Exoenzyme
Target: SapM
Drug effect: Inhibits a secreted alkaline phosphatase SapM activity to reduce intracellular mycobacterial survival in host macrophages.
Max phase: In vitro
Publication:
Fernández-Soto P, et al., 2021. Discovery of uncompetitive inhibitors of SapM that compromise intracellular survival of Mycobacterium tuberculosis. Sci Rep 11(1):7667.








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