14 Results for "

M. abscessus

" in MedChemExpress (MCE) Product Catalog:
Products (14)

14 Results for "M. abscessus" in MCE Product Catalog:

10
10 Cited Publications
Cat. No.: HY-136278
CAS No.: 146724-94-9
Purity:  98.10%
Synonyms: Diethylamine NONOate; NOC-18
Target:  

NO Synthase

Research Areas:  

Cardiovascular Disease

DETA NONOate (NOC 18) is an exogenous nitric oxide (NO) donor. DETA NONOate shows a slow release normal amounts of NO and long-acting .
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Cat. No.: HY-128866
CAS No.: 2332841-25-3
Target:  

Bacterial

Research Areas:  

Infection

TBAJ-876 is an orally active diarylquinoline anti-Mycobacterium agent. TBAJ-876 regulates energy metabolism by targeting the c and ε subunits of Mycobacterium tuberculosis F-ATP synthase, exerts bactericidal activity against replicating Mycobacterium tuberculosis, and retains activity against strains carrying the Rv0678 mutation. TBAJ-876 undergoes N-demethylation in vivo to form its major active metabolite TBAJ-876-M3, which has lower lipophilicity and hERG potassium channel binding affinity. TBAJ-876 is well tolerated in BALB/c mice and significantly reduces the colony-forming units of Mycobacterium tuberculosis in the lungs. In addition, TBAJ-876 exhibits inhibitory activity against Mycobacterium abscessus, reduces bacterial loads in the lungs and spleens of infected mice, and shows no antagonistic effect when used in combination with common antibiotics. TBAJ-876 can be used in studies related to tuberculosis and Mycobacterium abscessus pulmonary diseases .
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Cat. No.: HY-109028
CAS No.: 1801749-44-9
Synonyms: TR2-A
Ceclazepide (TR2-A), a CCK2R antagonist, is an orally active Mycobacterium abscessus inhibitor. Ceclazepide inhibits acid secretion in rats. Ceclazepide effectively suppresses the growth of M. abscessus wild-type strain and multiple subspecies. Ceclazepide inhibits M. abscessus growth within macrophages without causing harm .
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Cat. No.: HY-163181
CAS No.: 2810846-51-4
Target:  

Bacterial

Research Areas:  

Infection

MSU-43085 is an orally active MmpL3 inhibitor of Mycobacterium tuberculosis (Mtb). MSU-43085 effectively inhibits Mtb in an acute murine tuberculosis infection model. MSU-43085 can be used in tuberculosis research .
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Cat. No.: HY-143484
CAS No.: 2767443-97-8
Target:  

Bacterial

Research Areas:  

Infection

844-TFM is a NBTI (novel bacterial topoisomerase inhibitor) DNA gyrase inhibitor, with an IC50 of 1.5 μM. 844-TFM exhibits bactericidal properties against M. abscessus .
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Cat. No.: HY-149064
CAS No.: 2998587-72-5
Target:  

Bacterial

Research Areas:  

Infection

Antituberculosis agent-9 (Compound 5a) is an orally active antitubercular agent with an MIC of 0.5 μg/mL against H37Ra .
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Cat. No.: HY-159899
CAS No.: 2941327-87-1
DHFR-IN-22 (Compound 8) is a DHFR (Dihydrofolate Reductase) inhibitor belonging to the class of 2,4-diaminopyrimidine compounds. DHFR-IN-22 exhibits significant inhibitory activity against purified DHFR enzyme and major species of nontuberculous mycobacteria (NTM), namely Mycobacterium avium and Mycobacterium abscessus. It shows an IC50 of 1.1 nM and MIC of 1.5 μg/mL against M. abscessus, and an IC50 of 6.3 nM and MIC of 0.1 μg/mL against M. avium. Additionally, it demonstrates an IC50 of 2100 nM against human DHFR. DHFR-IN-22 holds potential for studying novel strategies to combat NTM infections .
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Cat. No.: HY-143483
CAS No.: 2767443-78-5
Target:  

Bacterial

Research Areas:  

Infection

NBTIs-IN-5 (Compound 5r) is a NBTI (Novel Bacterial Topoisomerase Inhibitor) DNA gyrase inhibitor with an IC50 of 1.5 μM against Mycobacterium abscessus (Mabs) DNA gyrase. NBTIs-IN-5 inhibits Mabs bamboo bacterial growth with an MIC90 of 0.4 μM .
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Cat. No.: HY-161890
Research Areas:  

Infection

Antimycobacterial agent-8 (Compound 49) is an inhibitor for DNA gyrase. Antimycobacterial agent-8 exhibits antibacterial activity against Mycobacterium tuberculosis and M. abscessus with MIC90 of 2.5 μM and 0.63 μM. Antimycobacterial agent-8 exhibits good plasma protein binding ability in mice .
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Cat. No.: HY-175825
Target:  

Bacterial

Research Areas:  

Infection

Antibacterial agent 291 (Compound 16) is an antibacterial agent. Antibacterial agent 291 has a potent antibacterial activity against Mycobacterium abscessus (M. abscessus) with a MIC of 16  μg/ML. Antibacterial agent 291 can be used for M. abscessus infections research .
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Cat. No.: HY-170519
CAS No.: 2248016-83-1
Target:  

Bacterial

Research Areas:  

Infection

K13787 is an acetohydroxyacid synthase (AHAS) inhibitor with antibacterial activity. K13787 has antibacterial activity against a variety of nontuberculous mycobacteria (NTM) and clarithromycin (CLR) resistant strains .
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Cat. No.: HY-183075
CAS No.: 1648720-01-7
Target:  

Bacterial ATP Synthase

Research Areas:  

Infection

ND-011458 is an Antibacterial agent, a QcrB inhibitor, and also an inhibitor of cytochrome bcc:aa3 oxidase function. ND-011458 binds to the QcrB subunit of cytochrome bcc:aa3 oxidase. ND-011458 inhibits ATP formation. When used in combination with Clofazimine (HY-B1046), ND-011458 exhibits bactericidal activity against Mycobacterium abscessus. ND-011458 can be used in studies related to Mycobacterium abscessus pulmonary infections .
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Cat. No.: HY-187375
Target:  

Bacterial

Research Areas:  

Infection Inflammation/Immunology

DL25 is a fungicide with an IC50 of 5.0 μg/mL against Mycobacterium tuberculosis DHQS. DL25 binds with high affinity to mycobacterial targets LysA, LpdA and SecA1. DL25 exhibits broad-spectrum anti-mycobacterial activity against multiple mycobacterial species and shows partial synergy with established anti-tuberculosis drugs. DL25 can be used in studies related to tuberculosis .
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Cat. No.: HY-161802
Target:  

Bacterial

Research Areas:  

Infection

Antibacterial agent 228 (Compound 8) inhibits the mycobacterial ribosome (IC50 for Mycobacterium smegmatis is 2.31 μM) and exhibits antibacterial activity against M. tuberculosis H37Rv (MIC=2 and 0.25 μg/mL for wildtype and Δ1258c mutant), M. abscessus ATCC 19977 (MIC=8 and 8 μg/mL for wildtype and Δ2780c mutant) and M. smegmatis (MIC=8 μg/mL) .
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