123 Results for "

A. baumannii ATCC 19606

" in MedChemExpress (MCE) Product Catalog:
Products (123)

123 Results for "A. baumannii ATCC 19606" in MCE Product Catalog:

49
49 Publications Verification
Cat. No.: HY-B0117
CAS No.: 220620-09-7
Synonyms: GAR-936
Research Areas:  

Infection Cancer

Tigecycline (GAR-936) is a broad-spectrum glycylcycline antibiotic. The mean inhibitory concentration (MIC) of Tigecycline for E. coli (MG1655 strain) is approximately 125 ng/mL . MIC50 and MIC90 are 1 and 2 mg/L for Acinetobacter baumannii (A. baumannii), respectively .
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49
49 Publications Verification
Cat. No.: HY-B0117D
CAS No.: 1229002-07-6
Synonyms: GAR-936 hydrate
Research Areas:  

Infection Cancer

Tigecycline (GAR-936) hydrate is a broad-spectrum glycylcycline antibiotic. The mean inhibitory concentration (MIC) of Tigecycline hydrate for E. coli (MG1655 strain) is approximately 125 ng/mL . MIC50 and MIC90 are 1 and 2 mg/L for Acinetobacter baumannii (A. baumannii), respectively .
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49
49 Publications Verification
Cat. No.: HY-B0117A
CAS No.: 197654-04-9
Synonyms: GAR-936 hydrochloride
Research Areas:  

Infection Cancer

Tigecycline hydrochloride (GAR-936 hydrochloride) is a broad-spectrum glycylcycline antibiotic. The mean inhibitory concentration (MIC) of Tigecycline for E. coli (MG1655 strain) is approximately 125 ng/mL . MIC50 and MIC90 are 1 and 2 mg/L for Acinetobacter baumannii (A. baumannii), respectively .
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49
49 Publications Verification
Cat. No.: HY-B0117C
Synonyms: GAR-936 tetramesylate
Research Areas:  

Infection Cancer

Tigecycline tetramesylate (GAR-936 tetramesylate) is a broad-spectrum glycylcycline antibiotic. The mean inhibitory concentration (MIC) of Tigecycline for E. coli (MG1655 strain) is approximately 125 ng/mL . MIC50 and MIC90 are 1 and 2 mg/L for Acinetobacter baumannii (A. baumannii), respectively .
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31
31 Cited Publications
Cat. No.: HY-113678
CAS No.: 1066-17-7
Synonyms: Polymyxin E
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

Colistin is an orally active polypeptide antibiotic. Colistin has excellent activity against various Gram-negative rod-shaped bacteria, including multidrug-resistant Pseudomonas aeruginosa, Acinetobacter baumannii and Klebsiella pneumoniae. Colistin is associated with nephrotoxicity. Colistin can be used for the research of infections caused by Gram-negative bacilli .
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12
12 Cited Publications
Cat. No.: HY-B0334
CAS No.: 68373-14-8
Synonyms: CP45899
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Sulbactam (CP45899) is a competitive, irreversible beta-lactamase inhibitor. Sulbactam shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex .
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12
12 Cited Publications
Cat. No.: HY-B0334A
CAS No.: 69388-84-7
Synonyms: CP45899 sodium
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Sulbactam (CP45899) sodium is a competitive, irreversible beta-lactamase inhibitor. Sulbactam sodium shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex .
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6
6 Cited Publications
Cat. No.: HY-117974
CAS No.: 1467157-21-6
Purity:  99.62%
Synonyms: ETX2514
Target:  

Bacterial

Research Areas:  

Infection

Durlobactam sodium salt (ETX2514) is a broad-spectrum β-lactamase inhibitor with IC50s of 4, 14 and 190 nM for Class A KPC-2, Class C AmpC and Class D OXA-24, respectively. For the treatment of drug-resistant Gram-negative bacteria including Acinetobacter baumannii .
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6
6 Cited Publications
Cat. No.: HY-136072
CAS No.: 2170848-99-2
Purity:  ≥99.0%
Target:  

Bacterial

Research Areas:  

Infection

Xeruborbactam disodium is a potent, ultra-broad-spectrum boronic acid beta-lactamase inhibitor. Xeruborbactam disodium inhibits key serine and metallo beta-lactamases at a nano molar range .
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1
1 Cited Publications
Cat. No.: HY-128780B
CAS No.: 2408422-41-1
Purity:  99.74%
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

SPR206 acetate is a polymyxin analog with antibiotic activity against Gram-negative pathogens, including multidrug-resistant (MDR) variants. SPR206 acetate has an anti-bacterial infection effect by interacting with the bacterium’s outer membrane. The MIC values of SPR206 acetate against Pseudomonas aeruginosa Pa14 and Acinetobacter baumannii NCTC13301 are both 0.125 mg/L .
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1
1 Cited Publications
Cat. No.: HY-116872
CAS No.: 4871-40-3
Purity:  99.33%
Target:  

Bacterial

Research Areas:  

Infection

MAC13772 is a BioA inhibitor with an IC50 of 0.28 μM against E. coli and an IC50 of 0.269 μM against A. baumannii. MAC13772 inhibits bacterial growth by targeting the biotin biosynthesis pathway. MAC13772 can be used in studies related to bacterial infections .
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1
1 Cited Publications
Cat. No.: HY-P2460
CAS No.: 172485-26-6
SMAP‑29 is a cathelicidin antimicrobial peptide with LPS‑binding and anti‑inflammatory properties. SMAP‑29 exerts broad‑spectrum antimicrobial activity against bacteria, fungi and multidrug‑resistant isolates. SMAP‑29 kills pathogens by permeabilizing bacterial membranes, inducing depolarization and cell lysis, and also inhibits inflammatory cytokines while reducing lethality in septic shock and pneumonia models. SMAP-29 can be used for research on bacterial infections, drug-resistant infections, septic shock .
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Cat. No.: HY-147429
CAS No.: 2379336-76-0
Purity:  99.09%
Synonyms: Abx MCP; RG6006
Target:  

Bacterial Liposome

Research Areas:  

Infection

Zosurabalpin (Abx MCP; RG6006) is a lipopolysaccharide (LPS) transport inhibitor that targets the LptB2FGC complex. Zosurabalpin blocks the transport of LPS from the inner membrane to the outer membrane, leading to intracellular toxic accumulation of LPS and bacterial death. Zosurabalpin exhibits potent antibacterial activity against carbapenem-resistant Acinetobacter baumannii (CRAB) and shows in vivo efficacy in mouse infection models. Zosurabalpin can be used for research on CRAB infections, including pneumonia and sepsis .
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Cat. No.: HY-103251
CAS No.: 1312473-63-4
Purity:  99.42%
Synonyms: LpxC-4
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

PF-5081090 (LpxC-4) is a potent LpxC inhibitor, is a rapidly bactericidal with broad-spectrum activity. PF-5081090 serves as a regulator of lipid A biosynthesis in Gram-negative pathogens .
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Cat. No.: HY-147349
CAS No.: 2410688-61-6
Purity:  99.54%
Synonyms: ANT3310 sodium
Research Areas:  

Infection

Pilabactam (ANT3310) sodium is a broad-spectrum covalent Serine β-Lactamase inhibitor, with IC50 values ranging from 1 nM to 175 nM (a panel of Serine β-Lactamase). Pilabactam sodium potentiates activity of β-lactam antibiotics against Carbapenem-Resistant Enterobacterales (CRE) and Acinetobacter baumannii (CRAB). Pilabactam sodium can be used in the research of bacterial infection .
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Cat. No.: HY-P2124
CAS No.: 20829-55-4
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

Cyclo(L-Trp-L-Trp) is an antibiotic, and shows antimicrobial activity. Cyclo(L-Trp-L-Trp) can inhibit A. baumannii, as well as Candida albicans, Bacillus subtilis, Micrococcus luteus, Saccharomyces cerevisiae, Aspergillus niger, Staphylococcus aureus. Cyclo(L-Trp-L-Trp) can be used in microbial infection research .
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Cat. No.: HY-136069
CAS No.: 2170834-63-4
Target:  

Bacterial

Research Areas:  

Infection

Xeruborbactam is a potent, ultra-broad-spectrum boronic acid beta-lactamase inhibitor. Xeruborbactam inhibits key serine and metallo beta-lactamases at a nano molar range .
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Cat. No.: HY-W006886
CAS No.: 945212-26-0
Research Areas:  

Others

Fmoc-(R)-2-(7-octenyl) Ala-OH is an unnatural Fmoc-protected amino acid and modification module. Fmoc-(R)-2-(7-octenyl) Ala-OH serves as a key building block for all-hydrocarbon cross-linking modification of antimicrobial peptides, and facilitates the generation of stapled peptide derivatives. When introduced into specific sites of the parent peptide, Fmoc-(R)-2-(7-octenyl) Ala-OH effectively increases the α-helix content of the peptide chain, thereby significantly enhancing its antimicrobial activity and proteolytic stability. Fmoc-(R)-2-(7-octenyl) Ala-OH is widely used in research on bacterial infections and the development of related antimicrobial agents . Stapled peptide is a specially chemically modified polypeptide. It locks the peptide chain into a stable α-helical structure by introducing a "staple"-like chemical bridge (usually an all-carbon backbone) at specific positions of the peptide chain.
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Cat. No.: HY-162959
CAS No.: 2254567-00-3
Research Areas:  

Infection

BWC0977 acts as an inhibitor of bacterial Topoisomerase. BWC0977 stabilizes single-strand DNA breaks, inhibits DNA supercoiling and decatenation activities, binds to GyrA and ParC residues, and activates the SOS response. BWC0977 can be used in research related to multidrug-resistant bacterial infections .
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Cat. No.: HY-127041
CAS No.: 88909-96-0
Purity:  98.00%
Target:  

Bacterial

Research Areas:  

Infection

Virstatin inhibits the pili system synthesis and prevents A. baumannii biofilm formation. Virstatin also inhibits dimerization of the transcriptional activator ToxT .
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