Fujii, Akira published the artcileProbiotics. Antistaphylococcal and antifibrinolytic activities of ω-amino- and ω-guanidinoalkanesulfonic acids, HPLC of Formula: 55788-44-8, the publication is Journal of Medicinal Chemistry (1975), 18(5), 502-5, database is CAplus and MEDLINE.
A series of 5 H2N(CH2)nSO3H (I, n = 1-5) was prepared by reacting the dibromoalkane with Na2SO3 followed by NH4OH, while the guanidino analogs (II, n = 2-5) were prepared from the corresponding I by reaction with S-ethylisothiourea sulfate [22722-03-8]. All 9 compounds significantly protected mice against Staphylococcus aureus, but did not inhibit growth of S. aureus in vitro, while most of I had antifibrinolytic activity. δ-Aminobutanesulfonic acid (I, n = 4) [14064-34-7] had significantly greater antistaphylococcal activity than γ-aminobutyryl-L-histidine [3650-73-5], and had antifibrinolytic activity equal to ε-aminohexanoic acid [60-32-2]. None of II had antifibrinolytic activity. Structure-activity relations are discussed.
Journal of Medicinal Chemistry published new progress about 55788-44-8. 55788-44-8 belongs to bromides-buliding-blocks, auxiliary class Bromide,Salt,Aliphatic hydrocarbon chain,Aliphatic hydrocarbon chain, name is Sodium 3-bromopropane-1-sulfonate, and the molecular formula is C3H6BrNaO3S, HPLC of Formula: 55788-44-8.
Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary