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Filtered Search Results
Medchemexpress LLC Tobramycin | 32986-56-4 | 99.9% | 25 G
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Tobramycin is a broad-spectrum aminoglycoside antibiotic used to treat moderate to severe bacterial infections caused by sensitive organisms. It is also used in pneumonia research, particularly related to *Pseudomonas aeruginosa*.
- Parenterally administered antibiotic
- Treats moderate to severe bacterial infections
- Used in pneumonia research related to *Pseudomonas aeruginosa*
- Purity of 99.9%
- Available as a solid
- Soluble in water and DMSO
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Medchemexpress LLC Erythromycin thiocyanate | 7704-67-8 | 96.4% | 1 ML
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Erythromycin thiocyanate, a macrolide antibiotic from Streptomyces erythreus, offers broad-spectrum antimicrobial activity. It inhibits bacterial 50S ribosomal subunits, blocking protein synthesis without affecting nucleic acid synthesis. The compound also demonstrates antitumor and neuroprotective effects in various research applications.
- Macrolide antibiotic
- Broad-spectrum antimicrobial activity
- Inhibits bacterial protein synthesis by targeting 50S ribosomal subunits
- Demonstrates antitumor effects
- Provides neuroprotective effects
- For research use only
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Medchemexpress LLC Thiamphenicol | 15318-45-3 | 99.6% | 500 MG
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Thiamphenicol is a methyl-sulfonyl derivative of Chloramphenicol and a broad-spectrum antimicrobial antibiotic. It functions by binding to the 50S ribosomal subunit, which inhibits protein synthesis and results in a bacteriostatic effect against Gram-negative, Gram-positive aerobic, and anaerobic bacteria. It is for research use only and not sold to patients.
- Significant post-antibiotic effect (PAE) on S. pneumoniae, S. aureus, and Escherichia coli.
- Powerful bactericidal effect against β-lactamase-positive and -negative H. influenzae.
- Good in vitro activity against difficult-to-treat multiply resistant pathogens.
- Rapid absorption and bioavailability over 70% (in vivo).
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Medchemexpress LLC Clindamycin palmitate hydrochloride | 25507-04-4 | 98.2% | 1 ML
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Clindamycin palmitate hydrochloride is a hydrochloride salt of the ester of clindamycin and palmitic acid. It functions as an antibacterial agent. While it is inactive in vitro, it rapidly hydrolyzes in vivo to become the antibacterially active clindamycin.
- Functions as an antibacterial agent.
- Inactive in vitro, but rapidly converts to active clindamycin in vivo.
- Available in various forms, including solid and solution.
- Strict storage conditions ensure product stability and efficacy.
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Medchemexpress LLC Vancomycin | 1404-90-6 | >99.0% | 50 MG
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Vancomycin is an antibiotic used for treating bacterial infections. It is a large glycopeptide compound with a molecular weight of 1450 Da. It has a unique mode of action, inhibiting the second stage of cell wall synthesis in susceptible bacteria. It is effective against many Gram-positive bacteria, including *Staphylococcus aureus*, *Staph. epidermidis*, *Str. agalactiae*, *Str. bovis*, *Str. mutans*, viridans streptococci, and enterococci. It can also be used to induce renal injury models in research.
- Antibiotic for bacterial infections
- Inhibits cell wall synthesis
- Alters cell membrane permeability
- Selectively inhibits ribonucleic acid synthesis
- Effective against many Gram-positive bacteria
- Useful for inducing renal injury models in research
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eMolecules Ethyl 3-((6-(4,5-dihydro-1H-benzo[d]azepin-3(2H)-yl)-2-(pyridin-2-yl)pyrimidin-4-yl)amino)propanoate hydrochloride | 1797983-09-5 | MFCD26142638 | 100mg
Ambeed | Ethyl 3-((6-(4,5-dihydro-1H-benzo[d]azepin-3(2H)-yl)-2-(pyridin-2-yl)pyrimidin-4-yl)amino)propanoate hydrochloride | 100mg | 525228335 | A608057 | | 1797983-09-5 | MFCD26142638 | 453.970 | C24H28ClN5O2
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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-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-15884 5mg Medchemexpress, GSK2838232 CAS:1443460-91-0 Purity:>98%
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Medchemexpress, HY-15884 5mg GSK2838232 CAS:1443460-91-0 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-13941B 5mg Medchemexpress, 1-Naphthyl PP1 (hydrochloride) CAS:956025-47-1 Purity:>98%
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Medchemexpress, HY-13941B 5mg 1-Naphthyl PP1 (hydrochloride) CAS:956025-47-1 1-Naphthyl PP1 hydrochloride (1-NA-PP 1 hydrochloride) is a selective inhibitor of src family kinases. 1-Naphthyl PP1 hydrochloride inhibits v-Src and c-Fyn, c-Abl, CDK2 and CAMK II with IC50s of 1.0, 0.6, 0.6, 18 and 22 μM, 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-13945 10mg Medchemexpress, NVP 231 CAS:362003-83-6 Purity:>98%
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Medchemexpress, HY-13945 10mg NVP 231 CAS:362003-83-6 NVP 231 is a potent, specific, and reversible ceramide kinase (CerK) inhibitor(IC50=12 nM) that competitively inhibits binding of ceramide to CerK. NVP 231 induces cell apoptosis by increasing DNA fragmentation and caspase-3 and caspase-9 cleavage. 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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Apexbio Technology LLC Anisomycin 22862-76-6 10mM (in 1mL DMSO)
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Anisomycin is an activator of c-Jun N-terminal kinase (JNK) a stress-activated protein kinase implicated in apoptotic signaling pathways regulating cell proliferation cell cycle progression and apoptosis It activates the JNK pathway at approximately 25 ng/ml concentration Experimental studies demonstrate anisomycin s capability to sensitize apoptosis-resistant cancer cell lines such as DU145 prostate carcinoma cells to Fas-mediated apoptosis as well as to induce apoptosis in leukemic HL-60 cells and primary mouse embryonic fibroblast cells by initiating JNK activation Anisomycin is thus widely utilized as a molecular tool in apoptosis-related research and insight into JNK-associated cell signaling
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Medchemexpress LLC Fenbendazole-d3 | 1228182-47-5 | 99.70% | 5 MG
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Fenbendazole-d3 is a deuterium-labeled version of Fenbendazole. It acts as a HIF-1α agonist, stimulating the HIF-1α-related GLUT1 pathway. Fenbendazole is an orally active benzimidazole anthelmintic agent known for its broad antiparasitic effects. It functions as a microtubule destabilizing agent, leading to cell-cycle arrest and mitotic cell death, and has also demonstrated antitumor activity in mice xenografted with wild-type p53.
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Reverses the inhibiting influence exerted by miR-143-5p on proliferation, colony-forming capacity, and migration in BT-549 and MCF-7 cells at 20 μM for 48 h
- Elevates the protein expression levels of HIF-1α and GLUT1 in BT-549 and MCF-7 cells at 10 μM for 48 h
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Medchemexpress LLC Ampicillin | 69-53-4 | 10 G
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Ampicillin is a broad-spectrum beta-lactam antibiotic targeting bacterial infections. It is active against a variety of gram-positive and gram-negative bacteria. Its molecular formula is C16H19N3O4S with a molecular weight of 349.40.
- Broad-spectrum beta-lactam antibiotic
- Active against gram-positive and gram-negative bacteria
- Molecular formula: C16H19N3O4S
- Molecular weight: 349.40
- Target: Bacterial
- Pathway: Anti-infection
- Storage: 4°C, protect from light; In solvent: -80°C for 6 months; -20°C for 1 month (protect from light)
- Inhibits the growth of E. coli in a dose-dependent manner
- Effective in alleviating symptoms of hemorrhagic enteritis
- Provides neuroprotection against ischemia-reperfusion brain injury
- Reduces MMPs activities and increases GLT-1 expression
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