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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
21 Results for "
B. cereus
" in MedChemExpress (MCE) Product Catalog:
Products (21)
21 Results for "B. cereus" in MCE Product Catalog:
1
Category:
other families Ketones, Aldehydes, Acids Plants Disease Research Fields Inflammation/Immunology
Target:
Cat. No.: HY-N9690
CAS No.: 64095-60-9
Synonyms: Longistylin A
Target:
Target:
Cat. No.: HY-W160679
CAS No.: 64700-15-8
7-(Carboxymethoxy)-4-methylcoumarin (Compound VIIIa) is the antibacterial and antifungal agent that exhibits inhibitory activity against S. aureus, B. cereus, S. lutea, C. albicans, C. glabrata, and C. parapsilosis .
Cat. No.: HY-N7454
CAS No.: 23893-13-2
Category:
Infection Macrolide Antibiotics Antibiotics Disease Research Antibacterial Endogenous metabolite Disease Research Fields
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Cat. No.: HY-170650
CAS No.: 33017-85-5
Research Areas:
SMase-IN-1 (Compound 4) is a bacterial sphingomyelinase enzyme (SMase) inhibitor (IC50 value for B. cereus SMase is 6.43 µM). SMase-IN-1 also inhibits eqBuChE (59.50% inhibition rate at 50 µM concentration). SMase-IN-1 forms a complex with Cu 2+ in biometal interactions. SMase-IN-1 reduces B. cereus-induced hemolysis on sheep erythrocytes .
Cat. No.: HY-N12096
CAS No.: 56691-88-4
Synonyms: α-Acetylsalazinic acid
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Cat. No.: HY-147878
CAS No.: 2448358-84-5
Antibacterial agent 111 (Compound 3) is an antibacterial agent with MIC values of 3.90 μg/mL and 0.49 μg/mL against B. cereus and K. pneumonia, respectively. Antibacterial agent 111 firmly binds with tyrosyl-tRNA synthetase residues .
Cat. No.: HY-N7105S
CAS No.: 1104979-33-0
Cat. No.: HY-N10281
CAS No.: 2701570-80-9
Category:
Infection Microorganisms Monophenols Ketones, Aldehydes, Acids Phenols Disease Research Fields
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Cat. No.: HY-W781265
CAS No.: 149466-04-6
Synonyms: L-755,805
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Research Areas:
BE 24566B is a polyketide fungal metabolite originally isolated from S. violaceusniger. It is active against B. subtilis, B. cereus, S. aureus, M. luteus, E. faecalis, and S. thermophilus (MICs=1.56, 1.56, 1.56, 1.56, 3.13, and 3.13 μg/mL, respectively). BE 24566B is an endothelin (ET) receptor antagonist (IC50s=11 and 3.9 μM for ETA and ETB receptors, respectively).
Cat. No.: HY-N15344
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Cat. No.: HY-137323
CAS No.: 109539-58-4
Category:
Target:
Cat. No.: HY-N12230
CAS No.: 1418291-70-9
Category:
Cat. No.: HY-N0987
CAS No.: 160623-47-2
Category:
Flavonoids Garcinia xanthochymus Hook. f. ex T. Anders. Guttiferae Plants Other Flavonoids
Target:
Cat. No.: HY-N8470
CAS No.: 54526-94-2
Synonyms: NSC 204855; U 40615
Steffimycin B is an anthracycline bacterial metabolite originally isolated from Streptomyces. It binds to DNA, preferentially intercalating at sites containing cytosine and guanine.2 Steffimycin B is cytotoxic to MCF-7, KB, NCI-H187, and Vero cells (IC50s=3.5, 6.75, 3.28, and 10.5 μM, respectively). It is active against M. tuberculosis (MIC=5.2 nM), B. cereus (MIC=1.56 μg/mL), and P. falciparum (IC50=2.19 μM).
Cat. No.: HY-122980
CAS No.: 120243-02-9
Synonyms: (S)-Myxochelin A
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Research Areas:
Myxochelin A is a microbial metabolite that has been found in A. disciformis and has diverse biological activities. It is active against Gram-positive bacteria, including B. cereus, S. aureus, and M. luteus, but not Gram-negative bacteria or fungi in an agar diffusion assay when used at a concentration of 80 μg/disc. Myxochelin A inhibits 5-lipoxygenase (5-LO) activity with an IC50 value of 1.9 μM for the recombinant human enzyme. It is cytotoxic to 26-L5 colon cancer cells when used at a concentration of 3 μg/mL.
Cat. No.: HY-W587414
CAS No.: 70253-62-2
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Research Areas:
Neospiramycin I is a macrolide antibiotic and a derivative of Spiramycin I (HY-N7141). Neospiramycin I is effective against the macrolide-sensitive KB210 strain of S. aureus, but ineffective against the macrolide-resistant KB224 strain, with minimum inhibitory concentrations (MIC) of 3.12 and greater than 100 µg/mL, respectively; it is also effective against B. cereus, B. subtilis, M. luteus, E. coli, and K. pneumoniae, with respective MIC values of 1.56, 3.12, 3.12, 0.2, 50, and 12.5 µg/mL. Neospiramycin I binds to the ribosomes of E. coli, with an inhibitory concentration 50 (IC50) of 1.2 µM. It protects mice from death in a type III S. pneumoniae infection model, with an effective dose 50 (ED50) of 399.8 mg/kg .
Cat. No.: HY-115442
CAS No.: 106359-61-9
NHNB is a selective HDAC8 inhibitor (IC50 = 66.0 μM) and Peptidoglycan N-acetylglucosamine (GlcNAc) deacetylases (PGNGdacs) inhibitor. NHNB shows antibacterial and bactericidal activity against B. anthracis and B. cereus. NHNB can be used for the research of acute myeloid leukemia, Bacillus anthracis infection, and Bacillus cereus infection .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
