Gadebusch H H, Schwind R, Lukaszow P, Whitney R, McRipley R J
J Antibiot (Tokyo). 1978 Oct;31(10):1046-58. doi: 10.7164/antibiotics.31.1046.
SQ 14,359 is a new cephamycin-type (7alpha-OCH3) antibiotic belonging to a series containing a 7alpha-ureidoacetyl substituent. The compound is the most potent extended spectrum derivative of this type yet reported, surpassing CS-1170 and cefoxitin by a wide margin. This activity in vitro which extends throughout the Enterobacteriaceae is particularly prominent against Gram-negative organisms that are producers of "cephalosporinase-type" beta-lactamases such as Enterobacter, Serratia, Citrobacter and indole-positive Proteus species. Superior activity also is demonstrated in vitro against streptococci, beta-lactamase-producing staphylococci, Haemophilus influenzae, Neisseria gonorrhoeae, and many Gram-negative pathogens resistant to aminoglycoside antibiotics. Experimental chemotherapeutic studies have confirmed these observations in wound and selected systemic infections in mice as well as acute pyelonephritis and meningitis in rats. The pharmacokinetics for each drug including antibiotic bound to serum was similar in both mice and rats. The pharmacokinetic profile in blood and cerebrospinal fluid favored SQ 14,359.
SQ 14,359是一种新型头孢霉素类(7α-OCH3)抗生素,属于含有7α-脲基乙酰取代基的系列化合物。该化合物是此类已报道的最有效的广谱衍生物,其活性远超CS-1170和头孢西丁。这种在整个肠杆菌科中均有表现的体外活性,对于产生“头孢菌素酶型”β-内酰胺酶的革兰氏阴性菌,如肠杆菌属、沙雷氏菌属、柠檬酸杆菌属和吲哚阳性变形杆菌属,尤为显著。在体外,它对链球菌、产β-内酰胺酶的葡萄球菌、流感嗜血杆菌、淋病奈瑟菌以及许多对氨基糖苷类抗生素耐药的革兰氏阴性病原体也表现出优异的活性。实验性化疗研究已在小鼠的伤口感染和选定的全身感染以及大鼠的急性肾盂肾炎和脑膜炎中证实了这些观察结果。包括与血清结合的抗生素在内,每种药物在小鼠和大鼠体内的药代动力学情况相似。血液和脑脊液中的药代动力学特征表明SQ 14,359具有优势。