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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T38298 | Tuberculosis inhibitor 3 | ||
Tuberculosis inhibitor 3 (compound 2i) exhibits potent anti-TB properties (MIC < 0.016 μg/mL) against both drug-sensitive and resistant MTB strains, along with acceptable pharmacokinetic profiles and oral bioavailability... | |||
T13223 | Tuberculosis inhibitor 1 | Others | |
Tuberculosis inhibitor 1 is a potent and non-cytotoxic inhibitor of trypanosoma brucei growth (EC50: 5 nM). | |||
T62087 | Tuberculosis inhibitor 4 | ||
Tuberculosis inhibitor 4 (compound 16) is a spirothiazolidinone based on mandelic acid that exhibits potent antimycobacterial action. The inhibitor inhibited 98% of Mycobacterium tuberculosis strain H37Rv at concentratio... | |||
T79510 | Tuberculosis inhibitor 7 | ||
Tuberculosis inhibitor 7 (compound 2d), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, exhibits potent activity against Mycobacterium tuberculosis and Mycobacterium marinum, with both displaying a MIC 90 of 0.6... | |||
T80927 | Tuberculosis inhibitor 10 | ||
Tuberculosis Inhibitor 10 moderately inhibits the enzyme MSMEG_6649 and potentiates the antimycobacterial activity of PAS [1]. | |||
T38359 | Dup-721 | Antibacterial | |
DuP-721 is a broad spectrum and orally active antibacterial agent. DuP-721 inhibits a variety of clinically susceptible and resistant bacteria, especially M. tuberculosis. | |||
T62086 | Tuberculosis inhibitor 5 | ||
Tuberculosis inhibitor 5 (Compound 11i) is a potent anti-tuberculosis agent with no apparent cytotoxicity. tuberculosis inhibitor 5 is an antimycobacterial biphenyl analogue. | |||
T80925 | Tuberculosis inhibitor 12 | ||
Tuberculosis Inhibitor 12, an oxadiazole derivative, effectively inhibits Mycobacterium tuberculosis, demonstrating inhibition rates of 82% and 78% at a concentration of 20 μM on 7H9-Tw-OADC media, respectively [1]. | |||
T79511 | Tuberculosis inhibitor 8 | ||
Tuberculosis inhibitor 8 (compound 3b), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, exhibits potent activity against both Mycobacterium tuberculosis and Mycobacterium marinum with an MIC 90 of 0.69 μM [1]. | |||
T80926 | Tuberculosis inhibitor 11 | ||
Compound 14, also known as Tuberculosis Inhibitor 11, enhances the antimycobacterial efficacy of antitubercular agent [1]. | |||
T79509 | Tuberculosis inhibitor 6 | ||
Tuberculosis inhibitor 6 (compound 2c), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, is highly active against Mycobacterium tuberculosis (MIC 90 of ≤1.66 μM) and Mycobacterium marinum (MIC 90 of 2.65 μM) [1]. | |||
T79512 | Tuberculosis inhibitor 9 | ||
Tuberculosis inhibitor 9 (compound 3d), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, exhibits potent activity against Mycobacterium tuberculosis and Mycobacterium marinum, with an MIC 90 of 0.64 μM for both o... | |||
T1426 | Pyrazinamide | Pyrazinoic acid amide,Pyrazinecarboxamide | Antibacterial , Antibiotic , Autophagy , Fatty Acid Synthase |
Pyrazinamide (Pyrazinecarboxamide), an antimycobacterial, is utilized therapeutically as an antitubercular agent, which is a synthetic pyrazinoic acid amide derivative. | |||
T9734 | InhA-IN-2 | CDK | |
InhA-IN-2 directly inhibits InhA and does not require activation by the catalase peroxidase KatG. | |||
T3582 | BTZ043 | Antibacterial , Antibiotic , DprE1 | |
BTZ043 is a DprE1 inhibitor with nanomolar bactericidal activity against Mycobacterium tuberculosis in vitro. | |||
T7342 | BM212 | Antibacterial | |
BM212 is an antimycobacterial compound.It inhibits the growth of laboratory and clinical isolate M. tuberculosis strains. | |||
T4044 | DprE1-IN-2 | Antibacterial , DprE1 | |
DprE1-IN-2 is an effective DprE1 inhibitor. | |||
T8411 | C-215 | Others | |
C-215 is a novel inhibitor of mycobacterial membrane protein large 3 (MmpL3). | |||
T10411 | AU1235 | Antibacterial | |
AU1235 is a Mycobacterium tuberculosis inhibitor. | |||
T8347 | Rifamycin S | Reactive Oxygen Species , ROS , Antibacterial , Antibiotic | |
Rifamycin S is a potent DNA-dependent RNA polymerase inhibitor,is a quinone and an antibiotic agnet against Gram-positive bacteria |