Mtb FtsZ, tubulin and Mtb H37Ra data of selected compounds 1–18.

NIAID Data Ecosystem2026-03-09 收录

数据链接：

https://figshare.com/articles/dataset/_i_Mtb_i_FtsZ_tubulin_and_i_Mtb_i_H_sub_37_sub_Ra_data_of_selected_compounds_1_18_/4054665 数据链接链接失效反馈

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资源简介：

Mtb FtsZ, tubulin and Mtb H37Ra data of selected compounds 1–18.

创建时间：

2016-10-22

A novel biosafety level 2 compliant tuberculosis infection model using a Δ leuD Δ panCD double auxotroph of Mycobacterium tuberculosis H37Rv and Galleria mellonella

结核病传播建模

抗结核药物

Mammalian infection models have contributed significantly to our understanding of the host-mycobacterial interaction, revealing potential mechanisms and targets for novel antimycobacterial therapeutic

NIAID Data Ecosystem70

Design and structural analysis of aromatic inhibitors of type II dehydroquinase dehydratase from Mycobacterium tuberculosis - compound 35c [3,4-dihydroxy-5-(3-nitrophenoxy)benzoic acid]

抗结核药物

抑制剂结构

Design and structural analysis of aromatic inhibitors of type II dehydroquinase dehydratase from Mycobacterium tuberculosis - compound 35c [3,4-dihydroxy-5-(3-nitrophenoxy)benzoic acid]

NIAID Data Ecosystem50

Data_Sheet_3_Screening of Compounds for Anti-tuberculosis Activity, and in vitro and in vivo Evaluation of Potential Candidates.xls

抗结核药物

抗结核候选药物评价

Tuberculosis (TB) is a debilitating infectious disease responsible for more than one million deaths per year. The emergence of drug-resistant TB poses an urgent need for the development of new anti-TB

NIAID Data Ecosystem30

Synthesis and in vitro studies for structure-based design of novel chalcones as antitubercular agents targeting InhA - SUPPLEMENTARY FILES FOR TABLES.docx

药物设计

抗结核药物

Table 1. Structure of the prepared chalcones Table 2. Synthesis of Chalcone Derivatives Table 3. Docking Score and Interactions of Designed Chalcone D

DataCite Commons2024-05-17 更新60

A competitive activity-based protein profiling platform yields cell wall synthesis inhibitors active against replicating and non-replicating Mycobacterium tuberculosis

抗结核药物

细胞壁生物学

The identification and validation of a small molecule's targets is a major bottleneck in the discovery process for tuberculosis antibiotics. Activity-based protein profiling (ABPP) is an efficient too

NIAID Data Ecosystem40

<i>Mtb</i> FtsZ, tubulin and <i>Mtb</i> H<sub>37</sub>Ra data of selected compounds 1–18.

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