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Filtered Search Results
Medchemexpress LLC Roxithromycin | 80214-83-1 | 1 G
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Roxithromycin (RU-28965) is an orally active semi-synthetic macrolide antibiotic. It inhibits protein biosynthesis in the elongation step by binding to the 50S bacterial ribosome. Roxithromycin exhibits antimicrobial, antiproliferative, anti-inflammatory, tumor vasculature inhibiting, and lung injury ameliorating effects.
- Inhibits protein biosynthesis by binding to 50S bacterial ribosome
- Active against Gram-positive and Gram-negative bacteria
- Displays antimicrobial, antiproliferative, and anti-inflammatory effects
- Inhibits tumor vasculature and ameliorates lung injury
- Reduces UVB-induced oxidative stress and keratinocyte apoptosis
- Induces apoptosis in senescent cells
- Protects against various bacterial infections in vivo
- Inhibits tumor angiogenesis and attenuates lung injury in animal models
- Modulates NF-κB and MAPK/ERK pathways
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Medchemexpress LLC Ampicillin | 69-53-4 | MFCD00005175 | >96.0% | 50 G
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Ampicillin is a broad-spectrum beta-lactam antibiotic effective against a variety of gram-positive and gram-negative bacteria. It has been shown to inhibit the growth of E. coli of swine origin in a dose-dependent manner and alleviate symptoms of hemorrhagic enteritis in pigs. Additionally, Ampicillin provides neuroprotection against ischemia-reperfusion brain injury by reducing MMPs activities and increasing GLT-1 expression.
- Broad-spectrum beta-lactam antibiotic
- Active against gram-positive and gram-negative bacteria
- Inhibits E. coli growth
- Alleviates hemorrhagic enteritis symptoms
- Provides neuroprotection against ischemia-reperfusion brain injury
- Storage at 4°C, protected from light
- In solvent, store at -80°C for 6 months or -20°C for 1 month, protected from light
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Research Products International Corp Erythromycin, 25 Grams
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Erythromycin is an antibiotic in the macrolide class. It is derived from the bacterium Streptomyces erythreus and inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit. This action effectively prevents the growth and reproduction of bacteria.
Employed as a selective agent in culture media to isolate bacteria that are sensitive to this antibiotic. Erythromycin is effective against a broad spectrum of bacteria, including Gram-positive bacteria (such as Streptococcus, Staphylococcus, and Corynebacterium species) and some Gram-negative bacteria (such as Haemophilus influenzae and Neisseria gonorrhoeae).
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UNITED STATES BIOLOGICAL CORPORATION G418 SULFATE GENE SOLN ST 20ML
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NC1132373 G418 SULFATE GENE SOLN ST 20ML
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Medchemexpress LLC Chlorquinaldol | 72-80-0 | 98.7% | 500 MG
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Chlorquinaldol (Chloquinan) is an antibacterial agent with potential use in topical skin conditions and vaginal infections. It is also a β-catenin/TCF4 inhibitor, demonstrating anti-proliferation, anti-migration, and apoptosis-inducing activity in cancer cells.
- Antibacterial agent for topical skin and vaginal infections.
- Acts as a β-catenin/TCF4 inhibitor.
- Demonstrates anti-proliferation and anti-migration activity.
- Induces apoptosis in cancer cells.
- Inhibits Wnt/β-catenin signaling in colorectal cancer cells.
- Reduces β-catenin acetylation, affecting interaction with TCF4.
- Inhibits stemness of colorectal cancer cells.
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FUJIFILM BIOSCIENCES INC PENICILLIN-STREPTOMYCIN SOLUTI
Penicillin-Streptomycin Solution (100x)
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Sigma Aldrich Fine Chemicals Biosciences Ansamitocin P-3 from Actinosynnema pretiosum >=90% (HPLC) | 66584-72-3 | MFCD00274586 | 1MG
Ansamitocin P-3 from Actinosynnema pretiosum >=90% (HPLC) | Purity: >=90% (HPLC) | Mol Wt: 635.14 | 66584-72-3 | MFCD00274586 | 1MG
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Takara Bio Aureobasidin A, 10mg
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Aureobasidin A (AbA) is a cyclic depsipeptide antibiotic, isolated from the filamentous fungus Aureobasidium pullulans R106, which is toxic to yeast at low concentrations (0.10.5 g/ml). Sensitive species include Saccharomyces cerevisiae, Schizosaccharomyces pombe, Candida glabrata, Aspergillus nidulans and A. niger. AbA inhibits a yeast enzyme, inositol phosphorylceramide (IPC) synthase, which is expressed from the AUR1 gene. Expression of a mutant gene, AUR1-C, in transformed yeast confers resistance to the drug.
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Research Products International Corp Cefoperazone, 10 G
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Cefoperazone Sodium Salt is a third-generation cephalosporin antibiotic. Cefoperazone inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs). This disruption interferes with the final stages of peptidoglycan synthesis in the bacterial cell wall, leading to structural instability and eventual cell lysis.
Cefoperazone is effective against a broad range of bacteria, both Gram-positive and Gram-negative. Cefoperazone Sodium Salt is often used as a selective agent in culture media to isolate bacteria that are sensitive to this antibiotic. Its inclusion allows for the specific growth of bacteria lacking resistance to cefoperazone.
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Medchemexpress LLC HY-15510 5mg Medchemexpress, Tenovin-6 CAS:1011557-82-6 Purity:>98%
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Medchemexpress, HY-15510 5mg Tenovin-6 CAS:1011557-82-6 Tenovin-6, an analog of Tenovin-1 (HY-13423), is an activator of p53 transcriptional activity. Tenovin-6 inhibits the protein deacetylase activities of purified human SIRT1, SIRT2, and SIRT3 with IC50s of 21 μM, 10 μM, and 67 μM, respectively. Tenovin-6 also inhibits dihydroorotate dehydrogenase (DHODH). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-14929A 5mg Medchemexpress, Migalastat (hydrochloride) CAS:75172-81-5 Purity:>98%
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Medchemexpress, HY-14929A 5mg Migalastat (hydrochloride) CAS:75172-81-5 Migalastat hydrochloride (GR181413A) is a potent and competitive inhibitor of α-galactosidase A (α-Gal A) with an IC50 of 0.04 μM for human α-Gal A. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-14852 5mg Medchemexpress, Tafamidis CAS:594839-88-0 Purity:>98%
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Medchemexpress, HY-14852 5mg Tafamidis CAS:594839-88-0 Tafamidis is a potent and selective transthyretin (TTR) stabilizer, shows comparable potency and efficacy to the mutumant homotetramers V30M-TTR, V122I-TTR and wild type WT-TTR, with EC50s of 2.7-3.2 μM. Tafamidis inhibits amyloidogenesis. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-14880B 5mg Medchemexpress, Bavisant (dihydrochloride hydrate) CAS:1103522-80-0 Purity:>98%
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Medchemexpress, HY-14880B 5mg Bavisant (dihydrochloride hydrate) CAS:1103522-80-0 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-15067 25mg Medchemexpress, DNQX CAS:2379-57-9 Purity:>98%
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Medchemexpress, HY-15067 25mg DNQX CAS:2379-57-9 DNQX (FG 9041), a quinoxaline derivative, is a selective, potent competitive non-NMDA glutamate receptor antagonist (IC50s = 0.5, 2 and 40 μM for AMPA, kainate and NMDA receptors, respectively). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-15066 5mg Medchemexpress, CNQX CAS:115066-14-3 Purity:>98%
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Medchemexpress, HY-15066 5mg CNQX CAS:115066-14-3 CNQX (FG9065) is a potent and competitive AMPA/kainate receptor antagonist with IC50s of 0.3 μM and 1.5 μM, respectively. CNQX is a competitive non-NMDA receptor antagonist. CNQX blocks the expression of fear-potentiated startle in rats[5]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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