K. Waisser et al., ANTITUBERCOLOTICS .66. NEW GROUPS OF POTENTIAL ANTITUBERCULOTICS - BIS(1-ARYLTETRAZOL-5-YL) DISULFIDES - STRUCTURE-ACTIVITY RELATIONSHIP, Collection of Czechoslovak Chemical Communications, 59(1), 1994, pp. 234-238
Oxidation of 1-aryltetrazole-5-thiols afforded bis(1-aryltetrazol-5-yl
) disulfides. The compounds were tested for antimycobactcrial activity
against Mycobacterium tuberculosis, M. kansasii, M. avium and M. fort
uitum. In the case of M. tuberculosis, the logarithm of minimum inhibi
tory concentration showed a parabolic dependence on hydrophobic substi
tuent constants. Although the compounds exhibited low to medium activi
ty, the most active derivative, bis(4-chlorophenyltetrazol-5-yl) disul
fide (III) was more effective against atypical strains than are the co
mmercial tuberculostatics used as standards.