3.2.1.35

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Showing 1-2 of 2 results for "3.2.1.35 " within Papers

Synthesis of benzoyl phenyl benzoates as effective inhibitors for phospholipase A2 and hyaluronidase enzymes.

Shaukath Ara Khanum et al.

Bioorganic & medicinal chemistry letters, 15(18), 4100-4104 (2005-07-05)

Benzoylation of (hydroxy phenyl) phenyl methanone 2a-g to benzoyl phenyl benzoates 4a-g, a benzophenone analogue, was achieved in good yield. All the newly synthesized compounds were evaluated for their phospholipase A2 [E.C. 3.1.1.4] and hyaluronidase [E.C. 3.2.1.35] enzyme inhibitory activity

Modification of functional arginine residues in purified bovine testicular hyaluronidase with butane-2, 3-dione.

P Gacesa et al.

Biochimica et biophysica acta, 661(2), 205-212 (1981-10-13)

Purified bovine testicular hyaluronidase (hyaluronate 4-glycanohydrolase, EC 3.2.1.35) was inactivated by butane-2,3-dione in either borate or Hepes buffer, pH 8.3. The presence of borate enhanced the inactivation process which followed pseudo-first-order kinetics with a calculated second-order rate constant of 13.54M-1

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