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Chemical Compound Review

AC1MYJCD     benzenesulfinate

Synonyms: SureCN22010, CHEBI:38100, ZINC04240615, ZINC06581647, ZINC12358706, ...
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High impact information on benzenesulfinic acid


Biological context of benzenesulfinic acid


  1. Heme oxygenase-1 gene activation by the NAD(P)H oxidase inhibitor 4-(2-aminoethyl) benzenesulfonyl fluoride via a protein kinase B, p38-dependent signaling pathway in monocytes. Wijayanti, N., Kietzmann, T., Immenschuh, S. J. Biol. Chem. (2005) [Pubmed]
  2. Expression of inducible nitric-oxide synthase and intracellular protein tyrosine nitration in vascular smooth muscle cells: role of reactive oxygen species. Fries, D.M., Paxinou, E., Themistocleous, M., Swanberg, E., Griendling, K.K., Salvemini, D., Slot, J.W., Heijnen, H.F., Hazen, S.L., Ischiropoulos, H. J. Biol. Chem. (2003) [Pubmed]
  3. Specificity and reactivity of human leukocyte elastase, porcine pancreatic elastase, human granulocyte cathepsin G, and bovine pancreatic chymotrypsin with arylsulfonyl fluorides. Discovery of a new series of potent and specific irreversible elastase inhibitors. Yoshimura, T., Barker, L.N., Powers, J.C. J. Biol. Chem. (1982) [Pubmed]
  4. LDL-associated phospholipase A does not protect LDL against lipid peroxidation in vitro. Schnitzer, E., Pinchuk, I., Fainaru, M., Lichtenberg, D., Yedgar, S. Free Radic. Biol. Med. (1998) [Pubmed]
  5. Aminoethyl benzenesulfonyl fluoride and its hexapeptide (Ac-VFRSLK) conjugate are both in vitro inhibitors of subtilisin kexin isozyme-1. Basak, S., Stewart, N.A., Chrétien, M., Basak, A. FEBS Lett. (2004) [Pubmed]
  6. Regioselectivity and reactivity in microsomal hydroxylation of a series of N-acyl- and N-sulfonylamines in rats. Shono, T., Ohmizu, Y., Toda, T., Oshino, N. Drug Metab. Dispos. (1981) [Pubmed]
  7. Synthesis and antiviral activity of P1' arylsulfonamide azacyclic urea HIV protease inhibitors. Huang, P.P., Randolph, J.T., Klein, L.L., Vasavanonda, S., Dekhtyar, T., Stoll, V.S., Kempf, D.J. Bioorg. Med. Chem. Lett. (2004) [Pubmed]
  8. [3-(1H-imidazol-4-yl)propyl]guanidines containing furoxan moieties: a new class of H3-antagonists endowed with NO-donor properties. Bertinaria, M., Stilo, A.D., Tosco, P., Sorba, G., Poli, E., Pozzoli, C., Coruzzi, G., Fruttero, R., Gasco, A. Bioorg. Med. Chem. (2003) [Pubmed]
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