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multi drug resistance strain mdr m tuberculosis atcc 35822  (ATCC)


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    ATCC multi drug resistance strain mdr m tuberculosis atcc 35822
    Multi Drug Resistance Strain Mdr M Tuberculosis Atcc 35822, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 191 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/multi+drug+resistance+strain+mdr+m+tuberculosis+atcc+35822/Mycobacterium+tuberculosis+(Zopf)+Lehmann+and+Neumann/10__1055_slash_s___0043___1775424-47-23-28
    Average 96 stars, based on 191 article reviews
    multi drug resistance strain mdr m tuberculosis atcc 35822 - by Bioz Stars, 2026-09
    96/100 stars

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    Activity Assay:

    Article Title: Synthesis, In Vitro and In Silico Molecular Docking Studies of Novel Phthalimide–Pyrimidine Hybrid Analogues to Thalidomide as Potent Antitubercular Agents
    Article Snippet: .. Antitubercular Activity towards Isoniazid, Cycloserine, Kanamycin, and Rifampin-Resistant M. Tuberculosis(ATCC 35822) Compounds 6a–f and 8a–f were further tested for antitubercular activity against the multi-drug-resistance strain (MDR) M. tuberculosis ATCC 35822 (isoniazid, cycloserine, Scheme 2 Synthesis of 2-(2-chloro-6-((3-alkylbenzylidene)amino)pyrimidin-4-yl)isoindoline-1,3-dione derivatives 6a–f 6 R 6a 3-NO2 6b 4-NO2 6c 4-Cl 6d 3,4-(OMe)2 6e 2-OH 6f 4-OH N O O N N Cl NH2 N O O N N Cl N EtOH, Et3N HO R R 4 5 6a–f r.t., 6–8 h Scheme 3 Synthesis of 2-(6-amino-2-hydrazineylpyrimidin-4-yl)isoindoline-1,3-dione 7 N O O N N Cl NH2 EtOH, Et3N H2N-NH2·H2O N O O N N NHNH2 NH2 4 7 r.t., 9 h Scheme 4 Synthesis of 2-(6-amino-2-(2-(arylidene)hydrazineyl)pyrimidin-4-yl)isoindoline-1,3-dione derivatives 8a–f EtOH, Et3N O H R N O O N N NHNH2 NH2 N O O N N NH2 HN N R 7 8a-f + 8 R 8a 3-NO2 8b 4-NO2 8c 4-Cl 8d 2-OH 8e 4-OH 8f 4-N(CH3)2 r.t., 2–11 h SynOpen 2025, 9, 73–83 kanamycin, and rifampin-resistant strain) using the microplate Alamar blue assay. ..

    Alamar Blue Assay:

    Article Title: Synthesis, In Vitro and In Silico Molecular Docking Studies of Novel Phthalimide–Pyrimidine Hybrid Analogues to Thalidomide as Potent Antitubercular Agents
    Article Snippet: .. Antitubercular Activity towards Isoniazid, Cycloserine, Kanamycin, and Rifampin-Resistant M. Tuberculosis(ATCC 35822) Compounds 6a–f and 8a–f were further tested for antitubercular activity against the multi-drug-resistance strain (MDR) M. tuberculosis ATCC 35822 (isoniazid, cycloserine, Scheme 2 Synthesis of 2-(2-chloro-6-((3-alkylbenzylidene)amino)pyrimidin-4-yl)isoindoline-1,3-dione derivatives 6a–f 6 R 6a 3-NO2 6b 4-NO2 6c 4-Cl 6d 3,4-(OMe)2 6e 2-OH 6f 4-OH N O O N N Cl NH2 N O O N N Cl N EtOH, Et3N HO R R 4 5 6a–f r.t., 6–8 h Scheme 3 Synthesis of 2-(6-amino-2-hydrazineylpyrimidin-4-yl)isoindoline-1,3-dione 7 N O O N N Cl NH2 EtOH, Et3N H2N-NH2·H2O N O O N N NHNH2 NH2 4 7 r.t., 9 h Scheme 4 Synthesis of 2-(6-amino-2-(2-(arylidene)hydrazineyl)pyrimidin-4-yl)isoindoline-1,3-dione derivatives 8a–f EtOH, Et3N O H R N O O N N NHNH2 NH2 N O O N N NH2 HN N R 7 8a-f + 8 R 8a 3-NO2 8b 4-NO2 8c 4-Cl 8d 2-OH 8e 4-OH 8f 4-N(CH3)2 r.t., 2–11 h SynOpen 2025, 9, 73–83 kanamycin, and rifampin-resistant strain) using the microplate Alamar blue assay. ..



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