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877950-01-1

中文名稱 LtaS-IN-1
英文名稱 LtaS-IN-1
CAS 877950-01-1
分子式 C24H17N3O5
分子量 427.41
MOL 文件 877950-01-1.mol
877950-01-1 結(jié)構(gòu)式 877950-01-1 結(jié)構(gòu)式

基本信息

中文別名
化合物 T11888
化合物L(fēng)TAS-IN-1
英文別名
LtaS-IN-1
(5-phenyl-1,3,4-oxadiazol-2-yl)carbamoyl]methyl 2-{naphtho[2,1-b]furan-1-yl}acetate
2-oxo-2-((5-phenyl-1,3,4-oxadiazole-2-yl)amino-)ethyl 2-(naphtho[2,1-b]furo-1-yl)acetate
Naphtho[2,1-b]furan-1-acetic acid, 2-oxo-2-[(5-phenyl-1,3,4-oxadiazol-2-yl)amino]ethyl ester
Bacterial,MDR,E. faecium,LtaSIN1,multidrug-resistant,inhibit,LtaS IN 1,anti-bacterial,Inhibitor

物理化學(xué)性質(zhì)

密度1.400±0.06 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)9.67±0.70(Predicted)
形態(tài)Solid
顏色Light yellow to yellow

常見問題列表

生物活性
LtaS-IN-1 (compound 1771) 是一種高效的小分子脂磷壁酸 (LTA) 抑制劑,可抑制耐多藥 (MDR) 大腸桿菌中脂磷壁酸 (LTA) 的合成,并可改變細(xì)胞壁的形態(tài)。LtaS-IN-1 單獨使用抑制腸球菌的生長的 MIC 值范圍從 0.5 μg/mL 到 64 μg/mL。LtaS-IN-1 與抗生素聯(lián)合使用幾乎可以完全抑制耐多藥的大腸桿菌生長。
靶點

MIC: 0.5 μg/mL (strain E1630); 0.5 μg/mL (strain E1590)

體外研究

LtaS-IN-1 (0-100 μM) inhibits strain E745 growth as a concentration-dependent manner. At the concentration 10 μM leads to an 60% reduction in the final OD600 for this strain. Meanwhile, LtaS-IN-1 does not affect E. faecium growth in control group. LtaS-IN-1 is against Enterococcus spp 28 strains with varying MIC values ranging from 0.5 μg/mL to 64 μg/mL. LtaS-IN-1 inhibits strain E1630 and E1590 with the MIC values of 0.5μg/mL. LtaS-IN-1 (20 μM) combines with either ampicillin (20 μg/mL), gentamicin (10 μg/mL), linezolid (5 μg/mL), daptomycin (10 μg/mL+50 μg/mL calcium chloride) or vancomycin (20 μg/mL) can inhibit strains E7128 and E7130 growth by 97-100%, while LtaS-IN-1 alone only gives 73% (strain E7128) and 8% (strain E7130) of growth inhibition, respectively.

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