23 Results for "

tubercular

" in MedChemExpress (MCE) Product Catalog:
Products (23)

23 Results for "tubercular" in MCE Product Catalog:

7
7 Cited Publications
Cat. No.: HY-N0804
CAS No.: 14259-46-2
Narirutin, one of the active constituents isolated from citrus fruits, has antioxidant and anti-inflammatory activities. Narirutin is a shikimate kinase inhibitor with anti-tubercular potency .
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1
1 Cited Publications
Cat. No.: HY-N0804R
CAS No.: 14259-46-2
Narirutin (Standard) is the analytical standard of Narirutin. This product is intended for research and analytical applications. Narirutin, one of the active constituents isolated from citrus fruits, has antioxidant and anti-inflammatory activities. Narirutin is a shikimate kinase inhibitor with anti-tubercular potency .
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Cat. No.: HY-N1377
CAS No.: 10176-66-6
Synonyms: Lysionotin
Nevadensin (Lysionotin), a natural flavonoid, is a selective human carboxylesterase 1 (hCE1) inhibitor with an IC50 of 2.64 μM. Nevadensin is more selective for hCE1 than hCE2 (IC50 of 132.8 μM). Nevadensin can induce apoptosis and DNA damage in cancer cells. Nevadensin has a variety of pharmacological effects such as anti-inflammatory, anti-tumour, anti-hypertensive, anti-tubercular, antitussive, antioxidant and anti-microbial activities .
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Cat. No.: HY-124781
CAS No.: 774589-47-8
Purity:  99.05%
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

ML406 is a small molecule probe that shows anti-tubercular activity via M.tuberculosis BioA (DAPA synthase) enzyme inhibition with an IC50 of 30 nM. M.tuberculosis BioA is an enzyme involved in biotin biosynthesis in M.tuberculosis .
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Cat. No.: HY-146120
CAS No.: 1845719-91-6
Target:  

Bacterial

Research Areas:  

Infection

Antitubercular agent-25 (Compound 28) is an anti-tubercular agent with an extracellular IC50 of 0.42 μM and an intracellular IC50 of 0.20 μM against M. tuberculosis H37Rv. Antitubercular agent-25 exhibits good metabolic stability .
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Cat. No.: HY-129943
CAS No.: 20605-40-7
Purity:  99.59%
Target:  

Bacterial

Research Areas:  

Infection

Benzothiohydrazide is an analogue of anti–tubercular agent Isoniazid. Benzothiohydrazide exhibits anti–tubercular activity, with MICs of 132 μM and 264 μM for M. tuberculosis wild type (H37Rv) and clinical mutant strains (IC1 and IC2) .
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Cat. No.: HY-W012813
CAS No.: 1193-79-9
2-Acetyl-5-methylfuran is a growth inhibitor of Mycobacterium tuberculosis, exhibiting an in vitro anti-tubercular activity with an MIC of 322.58 μM. 2-Acetyl-5-methylfuran demonstrates high safety and can be used for research related to tuberculosis .
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Cat. No.: HY-162684
Target:  

Bacterial

Research Areas:  

Infection Inflammation/Immunology

Antitubercular agent-46 (4B) is an anti-tubercular agent, with a MIC of 7.81 μg/ mL. Antitubercular agent-46 (4B) possesses antioxidant activity .
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Cat. No.: HY-119369
CAS No.: 2081969-24-4
Target:  

Bacterial

Research Areas:  

Infection

FadD32 Inhibitor-1 is a potent FadD32 inhibitor with anti-tubercular activity .
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Cat. No.: HY-147876
CAS No.: 1902712-34-8
Target:  

Bacterial Fungal

Research Areas:  

Infection

Antimicrobial agent-3 (Compound U10) is an antimicrobial agent against bacterial, fungal and tubercular infections .
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Cat. No.: HY-117990
CAS No.: 1403602-32-3
Target:  

Bacterial

Research Areas:  

Infection

GSK572A is a potent EchA6 inhibitor with an Kd value of 1.9 µM. GSK572A shows anti-tubercular activity .
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Cat. No.: HY-123451
CAS No.: 922491-46-1
Target:  

Bacterial

Research Areas:  

Infection

ACH-702 is a potent anti-tubercular agent. ACH-702 also shows broad-spectrum antibacterial activity .
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Cat. No.: HY-N8388
CAS No.: 34465-83-3
Collinin is a anti-tubercular agent, it can be isolated from leaves of Z. schinifolium. Collinin has an excellent anti-tuberculosis effect against multidrug-resistant (MDR), extensively drug-resistant (XDR) strains .
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Cat. No.: HY-146119
CAS No.: 1845719-43-8
Target:  

Bacterial

Research Areas:  

Infection

Antitubercular agent-24 (Compound 1) is an anti-tubercular agent with an extracellular IC50 of 0.83 μM and an intracellular IC50 of 0.17 μM against M. tuberculosis H37Rv .
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Cat. No.: HY-147819
CAS No.: 2522667-08-7
Research Areas:  

Infection

DNA Gyrase-IN-3 (Compound 28) is a bacterial DNA gyrase B inhibitor with IC50s of 5.41-15.64 µM for E. coli DNA gyrase. Anti-tubercular and antibacterial activity .
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Cat. No.: HY-147818
CAS No.: 2522666-80-2
Research Areas:  

Infection

DNA Gyrase-IN-2 (Compound 22a) is a bacterial DNA gyrase B inhibitor with IC50s of 3.29-10.49 and 4.41-5.61 µM for E. coli DNA gyrase and M. tuberculosis DNA gyrase. Anti-tubercular and antibacterial activity .
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Cat. No.: HY-146121
CAS No.: 1845720-46-8
Target:  

Bacterial

Research Areas:  

Infection

Antitubercular agent-26 (Compound 32) is an orally active anti-tubercular agent with an extracellular IC50 of 0.50 μM and an intracellular IC50 of 0.51 μM against M. tuberculosis H37Rv. Antitubercular agent-26 shows good metabolic stability, low risk of cardiotoxicity and no genotoxicity .
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Cat. No.: HY-124781R
CAS No.: 774589-47-8
Research Areas:  

Infection

ML406 (Standard) is the analytical standard of ML406. This product is intended for research and analytical applications. ML406 is a small molecule probe that shows anti-tubercular activity via M.tuberculosis BioA (DAPA synthase) enzyme inhibition with an IC50 of 30 nM. M.tuberculosis BioA is an enzyme involved in biotin biosynthesis in M.tuberculosis[1].
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Cat. No.: HY-149395
CAS No.: 1639438-67-7
Target:  

Bacterial

Research Areas:  

Infection

MmpL3-IN-3 (Compound 12) is a MmpL3 inhibitor. MmpL3-IN-3 shows a MIC of 0.1 μM against H37Rv. MmpL3-IN-3 shows good stability in mouse liver microsomes. MmpL3-IN-3 can be used for anti-tubercular research .
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Cat. No.: HY-N1377R
CAS No.: 10176-66-6
Synonyms: Lysionotin (Standard)
Nevadensin (Standard) (Lysionotin (Standard)) is the analytical standard of Nevadensin (HY-N1377). This product is intended for research and analytical applications. Nevadensin, a natural flavonoid, is a selective human carboxylesterase 1 (hCE1) inhibitor with an IC50 of 2.64 μM. Nevadensin is more selective for hCE1 than hCE2 (IC50 of 132.8 μM). Nevadensin can induce apoptosis and DNA damage in cancer cells. Nevadensin has a variety of pharmacological effects such as anti-inflammatory, anti-tumour, anti-hypertensive, anti-tubercular, antitussive, antioxidant and anti-microbial activities.
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