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Filtered Search Results
Selleck Chemical LLC Neomycin sulfate 50mg 1405-10-3
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Neomycin sulfate is an aminoglycoside antibiotic, used to treat bacteria infections. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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Cayman Chemical LexIthromycIn 25mg
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A macrolide antibiotic; a semisynthetic erythromycin derivative; improved pH stability and absorption over erythromycin; prevents protein synthesis; binds ribosome polypeptide exit tunnel
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Boston Bioproducts Inc Kanamycin (50 mg/ml, dH2O) - 100ml
Kanamycin (50 mg/ml dH2O) - 100ml (For Research Use and Further Manufacturing Only)
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Medchemexpress LLC HY-78131A 500mg Medchemexpress, (S)-(+)-Ibuprofen CAS:51146-56-6 Purity:>98%
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Medchemexpress, HY-78131A 500mg (S)-(+)-Ibuprofen CAS:51146-56-6 (S)-(+)-Ibuprofen is the S(+)-enantiomer of Ibuprofen that inhibits COX-1 and COX-2 activity with IC50s of 2.1 μM and 1.6 μM. (S)-(+)-Ibuprofen has analgesic, antiinflammatory and antipyretic effects. 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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STEMCELL Technologies Mifepristone, Size: 1 g
Mifepristone is a progesterone and glucocorticoid receptor antagonist (Ki = 0.64 and 0.1 nM, respectively; Attardi et al.; Song et al.; von Geldern et al.). It has been reported that Mifepristone is used in the treatment of leiomyomata, endometriosis, breast cancer, and meningioma (Mahajan et al.).CANCER RESEARCH· Inhibits the expressions of cyclin-dependent kinase 1 (CDK1) and cyclin-dependent kinase 2 (CDK2), leading to cell cycle arrest and apoptosis in endometrial epithelial cells and stromal cells in adenomyosis (Che et al.).· Induces cell cycle arrest and apoptosis in antiestrogen-resistant breast cancer cells in vitro (Gaddy et al.).
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STEMCELL Technologies Tunicamycin, Size: 10 mg
Tunicamycin is a nucleoside antibiotic and an N-acetylglucosamine phosphotransferase inhibitor (Contessa et al.). It also inhibits protein palmitoylation (Patterson & Skene.). Tunicamycin can be used to induce the unfolded protein response and investigate the mechanism of autophagy (Ding et al.). CANCER RESEARCH· Radiosensitizes human pancreatic cancer cells to chemotherapy (Contessa et al.).· Induces endoplasmic reticulum stress and autophagy in cancer cells (Ding et al.).
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Medchemexpress LLC Latanoprost | 130209-82-4 | 216074 | >99.85% | 100 MG
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Latanoprost is a prostaglandin F2α analogue primarily utilized in glaucoma research. This compound is capable of penetrating the cornea, where it is subsequently hydrolyzed by esterase into its active form, latanoprost acid. The acid then functions as an F-prostaglandin (FP) receptor agonist, efficiently reducing intraocular pressure by facilitating an increased outflow of aqueous humor via the uvea.
- Prostaglandin F2α analogue for research
- Passes through the cornea and is hydrolyzed to active acid form
- Acts as an F-prostaglandin (FP) receptor agonist
- Effectively lowers intraocular pressure (IOP)
- Increases aqueous humor outflow through the uvea
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Medchemexpress LLC Clindamycin hydrochloride | 21462-39-5 | 99.9% | 5 G
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Clindamycin hydrochloride is a semisynthetic lincosamide antibiotic that inhibits protein synthesis by acting on the 50S ribosomal subunit.
- Inhibits protein synthesis
- Semisynthetic lincosamide antibiotic
- High purity: 99.9%
- Solid appearance
- White to off-white color
- Store solid at 4°C, sealed, away from moisture
- Store in solvent at -80°C for 6 months or -20°C for 1 month, sealed, away from moisture
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Medchemexpress LLC Neomycin C (hexaacetate) | 66-86-4 | 97.1% | 1 MG
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Neomycin C hexaacetate is an impurity of Neomycin and a stereoisomer of Neomycin B. It exhibits in vitro antimicrobial activity against Staphylococcus epidermidis and Staphylococcus aureus, and can be used for the research of bacterial infection.
- Exhibits in vitro antimicrobial activity against Staphylococcus epidermidis and Staphylococcus aureus.
- Useful for bacterial infection research.
- Molecular weight of 974.96.
- Chemical formula C35H70N6O25.
- Solid appearance.
- White to off-white color.
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Medchemexpress LLC HY-12790 5mg Medchemexpress, CB1-IN-1 CAS:1429239-98-4 Purity:>98%
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Medchemexpress, HY-12790 5mg CB1-IN-1 CAS:1429239-98-4 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-19831 100mg , 4EGI-1 CAS:315706-13-9 Purity:98%
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Medchemexpress, HY-19831 100mg 4EGI-1 CAS:315706-13-9 Formula:C18H12Cl2N4O4S Kd: 25 μM (eIF4E/eIF4G) Purity:98% 4EGI-1 is an inhibitor of eIF4E/eIF4G interaction, with a K d of 25 μM against eIF4E binding. 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 Carbenicillin(Synonyms: Pyopen, Carbenicillin Sodium, Alpha-Carboxybenzylpenicillin, Carboxybenzylpenicillin), 250mg, CAS: B3412.
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Carbenicillin (CAS 4697-36-3) is a semi-synthetic penicillin derivative characterized by a broad-spectrum antibacterial profile Its bactericidal activity arises primarily through inhibition of bacterial cell wall biosynthesis specifically by interfering with penicillin-binding proteins (PBPs) thus impairing peptidoglycan formation This compound is widely utilized in biomedical research laboratories particularly for selecting bacteria carrying plasmids encoding carbenicillin resistance markers Carbenicillin enables effective differentiation between plasmid-containing and non-plasmid-containing bacterial colonies in molecular biology studies
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Medchemexpress LLC Suramin (sodium salt) | 129-46-4 | MFCD00003780 | 100.0% | 50 MG
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Suramin sodium salt is a reversible and competitive inhibitor of protein-tyrosine phosphatases (PTPases). It also potently inhibits sirtuins (SirT1, SirT2, SirT5), acts as a competitive inhibitor of reverse transcriptase (DNA topoisomerase II), and functions as a potent SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibitor. Additionally, it efficiently inhibits IP5K and acts as an antiparasitic, anti-neoplastic, and anti-angiogenic agent.
- Reversible and competitive PTPases inhibitor
- Potent inhibitor of sirtuins (SirT1, SirT2, SirT5)
- Competitive inhibitor of reverse transcriptase (DNA topoisomerase II)
- Potent SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibitor
- Efficiently inhibits IP5K
- Acts as an antiparasitic, anti-neoplastic, and anti-angiogenic agent
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Research Products International Corp Ampicillin Trihydrate 5 G
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Ampicillin is a broad-spectrum, beta-lactam antibiotic that belongs to the penicillin group. Ampicillin trihydrate is commonly employed in molecular biology techniques, such as bacterial culture studies and cloning experiments.
Ampicillin interferes with bacterial cell wall synthesis, leading to cell lysis and inhibiting bacterial growth. It is frequently used in the preparation of selective media for the cultivation of bacteria harboring ampicillin resistance genes.
Researchers use ampicillin as a tool to maintain sterile conditions in bacterial cultures and to selectively culture bacteria that have been genetically engineered to resist the antibiotic. This is particularly useful in molecular cloning experiments, where the presence of ampicillin helps select for the successful incorporation of plasmids carrying ampicillin resistance genes.
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Medchemexpress LLC Trimethoprim-d3 | 1189923-38-3 | MFCD16039497 | 99.2% | 1 MG
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Trimethoprim-d3 is the deuterium-labeled form of Trimethoprim, a bacteriostatic antibiotic that functions as an orally active dihydrofolate reductase inhibitor. It exhibits activity against a broad spectrum of Gram-positive and Gram-negative aerobic bacteria.
- It can be utilized as a tracer in various applications.
- It serves as an internal standard for quantitative analysis using techniques such as NMR, GC-MS, or LC-MS.
- Deuteration can potentially influence the pharmacokinetic and metabolic profiles of drugs.
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