PeptideDB

TBI-166

CAS: 1353734-12-9 F: C32H30F3N5O3 W: 589.61

TBI-166, a riminophenazine analogue, is an orally active anti-tuberculosis agent with fewer adverse reactionsthan the le
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Bioactivity TBI-166, a riminophenazine analogue, is an orally active anti-tuberculosis agent with fewer adverse reactions than the lead riminophenazine compound, Clofazimine (HY-B1046) [1][2][3].
Invitro TBI-166 抑制 M. tuberculosis H37Rv 复制 (MIC: 0.063 μg/mL),对 16 种药物敏感的临床分离株 (分枝杆菌属) 也有效,MIC 为 0.005-0.15μg/mL[1]。 TBI-166 (0-1 μg/mL,3 天) 抑制 M. tuberculosis 感染的 J774A.1 细胞内 M. tuberculosis[1].
In Vivo TBI-166 (10-80 mg/kg,口服,8 周) 在慢性小鼠 M. tuberculosis H37Rv 感染模型中表现出抗结核活性[1]。TBI-166 在小鼠体内显示出 LD50 值超过 3,000 mg/kg[1]。TBI-166 的半衰期较短 (41.25 h),可降低皮肤色素沉着的可能性[2]。 Animal Model:
Name TBI-166
CAS 1353734-12-9
Formula C32H30F3N5O3
Molar Mass 589.61
Appearance Solid
Transport Room temperature in continental US; may vary elsewhere.
Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Reference [1]. Xu J, et al. In Vitro and In Vivo Activities of the Riminophenazine TBI-166 against Mycobacterium tuberculosis. Antimicrob Agents Chemother. 2019 Apr 25;63(5):e02155-18. [2]. Zhu H, et al. Activity of Clofazimine and TBI-166 against Mycobacterium tuberculosis in Different Administration Intervals in Mouse Tuberculosis Models. Antimicrob Agents Chemother. 2021 Mar 18;65(4):e02164-20. [3]. Ding Y, et al. Superior Efficacy of a TBI-166, Bedaquiline, and Pyrazinamide Combination Regimen in a Murine Model of Tuberculosis. Antimicrob Agents Chemother. 2022 Sep 20;66(9):e0065822.