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Filtered Search Results
Medchemexpress LLC Medroxyprogesterone acetate-d3 | 98.1% | 389.54 g/mol | C24H31D3O4 | 10 MG
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Medroxyprogesterone acetate-d3 is the deuterated analog of medroxyprogesterone acetate, provided as an analytical internal standard for quantitative LC-MS and related mass spectrometry applications. It offers an isotopic match to the target analyte to improve accuracy and correct for matrix effects during sample preparation and analysis.
- Deuterated internal standard for LC-MS quantitation.
- Purity: 98.13% (typical, verified by HPLC).
- Molecular weight 389.54 g/mol.
- Chemical formula C24H31D3O4.
- Supplied in milligram quantities suitable for analytical use.
- Suitable for standard curve preparation and recovery experiments.
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eMolecules 2170694-04-7 | Medchem Express | IRAK4-IN-21 | 5mg | 785215422 | HY-151363 | 513.577 | C28H28FN7O2
Medchem Express | Biotin-PEG4-NHS ester | 50mg | 527574014 | HY-140889 | 459426-22-3 | MFCD08458915 | 588.670 | C25H40N4O10S
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AG Scientific Inc Hygromycin B in Water, 10 ML
The concentration of Hygromycin B in DI water is 100mg/ml. Hygromycin B is an aminoglycoside antibiotic effective against bacteria, fungi, and eukaryotic cells that are isolated from Streptomyces hygroscopicus. It is composed of amino groups attached to glycosides, that bind the 30s ribosomal subunits. This action causes the mRNA sequence to be misread, resulting in protein synthesis inhibition. Hygromycin B is also an antiviral agent, which works as a standard section antibiotic in gene experiments.CAS Number: 31282-04-09Molecular Weight: 527.5 DaChemical Formula: C20H37N3O13Storage Temperature: +4CResearch or further manufacturing use only, not for food or drug use.
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Sigma Aldrich Fine Chemicals Biosciences Ofloxacin fluoroquinolone antibiotic | 82419-36-1 | MFCD00226105 | 10G
Ofloxacin fluoroquinolone antibiotic | Purity: >=99% (HPLC) | Mol Wt: 361.37 | 82419-36-1 | MFCD00226105 | 10G
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Enzo Life Sciences Tobramycin (1g). CAS: 32986-56-4
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Aminoglycoside antibiotic with similar structure to the kanamycins and the gentamycins. Used in the treatment of respiratory infection and cystic fibrosis. Alternative name: Deoxykanamycin B, Distobram, Gernebcin, Obramycin, Tobradistin. Formulation: Free base. Appearance: White to off-white powder. Solubility: Soluble in water; very slightly soluble in 100% ethanol. Long Term Storage: +4°C.
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eMolecules 1629125-65-0 | Medchem Express | BMS-978587 | 2mg | 446269441 | HY-18769 | MFCD29924711 | 437.584 | C26H35N3O3
Medchem Express | Neoglycyrol | 1mg | 533803609 | HY-N3961 | 23013-84-5 | MFCD10566621 | 366.369 | C21H18O6
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Medchemexpress LLC Vancomycin (Standard) | 1404-90-6 | 95.92% | 50 MG
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Vancomycin (Standard) is the analytical standard of Vancomycin, intended for research and analytical applications. It is an antibiotic used for the treatment of bacterial infections.
- The compound is the grade of analytical standard, which is the reference standard supplied assay.
- It is commonly used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
- Application in disease research: Antibacterial.
- Initial source: Endogenous metabolite, human gut microbiota metabolites, microorganisms.
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Medchemexpress LLC HY-108465 5mg Medchemexpress, Pyr3 CAS:1160514-60-2 Purity:>98%
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Medchemexpress, HY-108465 5mg Pyr3 CAS:1160514-60-2 Pyr3 is a selective inhibitor of transient receptor potential canonical channel 3 (TRPC3), with an IC50 of 700 nM for TRPC3-mediated Ca2+ influx. 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 Retapamulin,10mg CAS# 224452-66-8
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Retapamulin is a pleuromutilin antibiotic [1].Retapamulin is developed for topical treatment of skin infections which is mainly caused by gram-positive organisms, β-hemolytic streptococci and coagulase-negative staphylococci. Retapamulin is especially used against those drug resistance strains. In the in vitro studies, retapamulin demonstrates potent activity and a broad spectrum. It shows excellent antimicrobial activities against S. aureus, S. epidermidis, S. saprophyticus, S. pyogenes, S. agalactiae and Viridans group streptococci with MIC50 values of 0.06μg/ml, 0.06μg/ml, 0.12μg/ml, 0.008μg/ml, 0.016μg/ml and 0.03μg/ml, respectively. Retapamulin plays its antibiotic role through binding to a unique site of the bacterial ribosome [1, 2]. Other sizes are also available. Please inqury us for quote.
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Apexbio Technology LLC Amoxicillin trihydrate 61336-70-7 1g
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Amoxicillin trihydrate (CAS 61336-70-7) is a small-molecule inhibitor targeting bacterial cell wall synthesis It is designed to inhibit peptidoglycan cross-linking thereby disrupting bacterial cell wall biosynthesis and resulting in cell lysis Amoxicillin trihydrate exerts its biological activity primarily through inhibition of bacterial transpeptidase enzymes involved in cell wall synthesis In in vitro studies Amoxicillin trihydrate demonstrates bactericidal activity with reported minimum inhibitory concentration (MIC) values of approximately 0 01 g/ml for Streptococcus viridans 0 25 g/ml for Bacillus anthracis and 50 g/ml for Retterella indica Based on these pharmacological properties Amoxicillin trihydrate holds research potential in antibacterial susceptibility testing microbial growth inhibition studies and in vitro pharmacological investigations
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Medchemexpress LLC Chloramphenicol | 56-75-7 | 100.0% | 250 MG
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Chloramphenicol is an orally active, potent, and broad-spectrum antibiotic with antibacterial activity. It represses the oxygen-labile transcription factor and hypoxia inducible factor-1 alpha (HIF-1α) in hypoxic A549 and H1299 cells. It also suppresses the mRNA levels of vascular endothelial growth factor (VEGF) and glucose transporter 1, leading to decreased VEGF release. Chloramphenicol can be used for anaerobic infections and lung cancer research.
- Inhibits HIF-1α pathway in NSCLC cells
- Induces autophagy in NSCLC cells
- Inhibits bacterial and mitochondrial protein synthesis
- Induces matrix metalloproteinase (MMP)-13 expression
- Activates JNK and PI-3K/Akt signaling
- Inhibits peptide bond formation by acting on the 50S subunit of bacterial 70S ribosomes
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Medchemexpress LLC HY-100225 5mg Medchemexpress, ME0328 CAS:1445251-22-8 Purity:>98%
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Medchemexpress, HY-100225 5mg ME0328 CAS:1445251-22-8 ME0328 is a potent and selective ARTD3 / PARP3 inhibitor with an IC 50 of 0.89±0.28 μM. 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 IRAK4-IN-4 100mg | 1850276-58-2 | 100 MG
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IRAK4-IN-4 is a small-molecule research inhibitor of interleukin-1 receptor-associated kinase 4 (IRAK4) with low-nanomolar potency. It is supplied as a light yellow solid, with molecular formula C22H16N2O2, molecular weight 340.37 g/mol, and high analytical purity. Solubility and storage guidance are provided for in vitro and in vivo use.
- Low-nanomolar IRAK4 potency (IC50 2.8 nM).
- Also inhibits cGAS (IC50 2.1 nM).
- High purity (99.55%).
- Soluble in DMSO (25 mg/mL); in vivo formulation protocols provided.
- Light yellow solid with recommended storage conditions for powder and solutions.
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Medchemexpress LLC Acp-5862 | 2230757-47-6 | 98.3% | C26H23N7O3 | 10MG
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ACP-5862 is the major active, circulating, pyrrolidine ring-opened metabolite of acalabrutinib that inhibits Bruton tyrosine kinase (BTK). It has been characterized for its contribution to acalabrutinib's pharmacological activity and displays potent BTK inhibition alongside weak, time-dependent inactivation of select cytochrome P450 enzymes. Supplied for research use with supporting analytical documentation.
- Potent BTK inhibition (IC50 ≈ 5.0 nM).
- Major circulating metabolite of acalabrutinib.
- Weak time-dependent inactivator of CYP3A4 and CYP2C8.
- Available as solid and as a DMSO solution.
- High analytical purity (~98.3% by HPLC).
- Supplied with certificate of analysis and safety data sheet.
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Medchemexpress LLC HY-12353A 10mg Medchemexpress, Pimodivir CAS:1629869-44-8 Purity:>98%
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Medchemexpress, HY-12353A 10mg Pimodivir CAS:1629869-44-8 Pimodivir (VX-787) is an orally bioavailable inhibitor of influenza A virus polymerases through interaction with the viral PB2 subunit. 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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