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129791-92-0

中文名稱 利福拉齊
英文名稱 Rifalazil
CAS 129791-92-0
分子式 C51H64N4O13
分子量 941.07
MOL 文件 129791-92-0.mol
129791-92-0 結(jié)構(gòu)式 129791-92-0 結(jié)構(gòu)式

基本信息

中文別名
利福拉齊
3'-羥基-5'-(4-異丁基-1-哌嗪)苯嗪利福霉素
3'-羥基-5'-(4-異丁基-1-哌嗪)苯噁嗪利福霉素
英文別名
KRM 1648
RIFALAZIL
Rifalazil USP/EP/BP
3'-Hydroxy-5'-(4-isobutylpiperazinyl)benzoxazinorifamycin
1-Deoxy-1'-dehydro-1-oxo-3'-hydroxy-5'-[4-(2-methylpropyl)piperazino]rifamycin VIII
5,12-Dihydroxy-2,4-dimethyl-10-[4-(2-methyl-propyl)-l-piperazinyl]-2,7-[oxy(5-acetoxy-7,9-dihydroxy-3-methoxy-4,6,8,10,14-pentamethyl-15-oxo-l,ll,13-pentadecatriene-l,15-diyl)imino]-6H-benzofuro[4,5-a]phenoxazine-l(2H),6-dione
所屬類別
原料藥:利福霉素類藥

物理化學(xué)性質(zhì)

熔點(diǎn)195-200° (dec)
沸點(diǎn)1065.6±65.0 °C(Predicted)
密度1.36±0.1 g/cm3(Predicted)
儲(chǔ)存條件4°C, away from moisture
溶解度DMSO: 8.33 mg/mL (8.85 mM)
酸度系數(shù)(pKa)4.28±0.70(Predicted)
形態(tài)Solid
顏色Blue to dark blue
利福拉齊價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2026/06/05HY-105099利福拉齊
Rifalazil
129791-92-05 mg1400元
2026/06/05HY-105099利福拉齊
Rifalazil
129791-92-010 mg2200元
2026/06/05HY-105099利福拉齊
Rifalazil
129791-92-025 mg4300元

常見問(wèn)題列表

生物活性
Rifalazil (ABI-1648; KRM-1648) 是利福霉素衍生物,可抑制細(xì)菌依賴 DNA 的 RNA 聚合酶 (RNA polymerase) 并阻斷 RNA 聚合酶中的 β 亞基從而殺死細(xì)菌感染的細(xì)胞。Rifalazil (ABI-1648; KRM-1648) 是一種抗生素 (antibiotic),對(duì)分枝桿菌,革蘭氏陽(yáng)性細(xì)菌,幽門螺桿菌,肺炎衣原體和沙眼衣原體有抑制作用,其 MIC 值在 0.00025 至 0.0025 μg/ml 之間。Rifalazil (ABI-1648; KRM-1648) 有潛力用于衣原體感染,梭菌相關(guān)性腹瀉菌感染?(CDAD) 和結(jié)核病 (TB) 研究的相關(guān)研究。
靶點(diǎn)

IC50: RNA polymerase

體外研究

Rifalazil exhibits antimicrobal activity against Gram-positive enteric bacteria, inhibits Clostridium difficile , Clostridium perfringens , Bacteroides fragilis with MIC 50 value of 0.0015, 0.0039, 0.0313 μg/ml, respectively. Rifalazil exhibits antimicrobal activity against Gram-negative enteric bacteria, inhibits Escherichia coli and Klebsiella pneumoniae with MIC 50 value of 16 and 16 μg/ml, respectively. Rifalazil exhibits antimicrobal activity against non-enteric Gram-positive bacteria, inhibits Methicillin-susceptible Staphylococcus aureus , Methicillin-resistant S. aureus , Methicillin- and quinolone-resistant S. aureus , Staphylococcus epidermidis , Streptococcus pyogenes , Streptococcus pneumoniae with MIC 50 value of 0.0078, 0.0078, 0.0078, 0.0078, 0.0002, 0.0001 μg/ml, respectively. Rifalazil exhibits antimicrobal activity against Helicobacter pylori , Chlamydia pneumoniae and Chlamydia trachomatis with MIC 50 value of 0.004, 0.000125 and 0.00025 μg/ml, respectively.

體內(nèi)研究

Rifalazil (oral gavage; 20, 25, and 150 mg/kg; 6-8 weeks) combines with isoniazid (INH) for 6 weeks or greater significantly reduced the number of mice per group in which M. tuberculosis is detected in both spleens and lungs compared to the reductions for the early and late controls. And the addition of Pyrazinamide (PZA) does not significantly improve RLZ-INH therapy at any time point.

Animal Model: Female CD-1 mice infected with 5.2 × 10 7 viable mycobacteria
Dosage: 20, 25, and 150 mg/kg; 6-8 weeks
Administration: Oral gavage
Result: Combined with isoniazid (INH) showed its potential for short-course treatment of Mycobacterium tuberculosis infection.
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