Zsolnai, Tibor published the artcileAntimicrobial action of potential thiol reagents, Category: iodides-buliding-blocks, the publication is Zentralblatt fuer Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene, Abteilung 1: Medizinisch-Hygienische Bakteriologie, Virusforschung und Parasitologie, Originale (1970), 214(4), 507-17, database is CAplus.
The bacteriostatic, fungistatic, trichomonastatic, amebicidal and acaricidal activity of 58 compounds which react with SH groups, was studied. Some compounds were active in vitro, but none in vivo. In vitro cysteine (I), thioglycolate, serum, and peptone inhibited the bacteriostatic activity, suggesting a mechanism of action which involves SH-containing enzymes. XRCHCO2Et (R = H or alkyl, X = I or Br) showed a strong antimicrobial activity which diminished for R = alkyl. Of several α-bromocarbonyl compounds and α-bromonitriles, the highest activity was shown by ω-bromoacetophenone (II). Most β-nitrostyrene derivatives were very active, especially those with an electrophilic substituent in para position. Very strong bacteriostatic and fungistatic activity was shown by α-bromostyrene and α,β-dibromostyrene (III). An especially marked activity was shown by tetraiodoethylene. A broad spectrum of antibacterial activity was shown by 4-nitroquinoline 1-oxide. High activity was shown by RHgX (R = Et, 4-HO2CC6H4 and X = Cl, 2-NaO2CC6H4S) and by p-RC6H4As(SCH2CO2H)2 (R = Cl or NH2).
Zentralblatt fuer Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene, Abteilung 1: Medizinisch-Hygienische Bakteriologie, Virusforschung und Parasitologie, Originale published new progress about 31253-08-4. 31253-08-4 belongs to iodides-buliding-blocks, auxiliary class Iodide,Ester, name is Ethyl 2-Iodopropionate, and the molecular formula is C19H36BNO2Si, Category: iodides-buliding-blocks.
Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com