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Filtered Search Results
Selleck Chemical LLC Anisomycin 10mg 22862-76-6 Flagecidin
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Anisomycin (Flagecidin) is a bacterial antibiotic isolated from Streptomyces griseolus, which inhibits protein synthesis, and also act as a JNK activator. Anisomycin upregulates autophagy and increases apoptosis. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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Medchemexpress LLC HY-100611 5mg Medchemexpress, CaCCinh-A01 CAS:407587-33-1 Purity:>98%
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Medchemexpress, HY-100611 5mg CaCCinh-A01 CAS:407587-33-1 CaCCinh-A01 is an inhibitor of both TMEM16A and calcium-activated chloride channel ( CaCC ) with IC 50 s of 2.1 and 10 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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eMolecules 1000669-72-6 | Medchem Express | KW-2449 | 5mg | 446258113 | HY-10339 | MFCD18385006 | 332.407 | C20H20N4O
Ambeed | 4455-Tetramethyl-2-(3-(methylsulfonyl)phenyl)-132-dioxaborolane | 1g | 525023228 | A123341 | 1001185-88-1 | MFCD14584690 | 282.160 | C13H19BO4S
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Medchemexpress LLC T025 | 2407433-00-3 | 99.6% | 382.42 | 100 MG
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T025 is an orally active and highly potent inhibitor of Cdc2-like kinase (CLKs), demonstrating Kd values of 4.8, 0.096, 6.5, 0.61, 0.074, 1.5, and 32 nM for CLK1, CLK2, CLK3, CLK4, DYRK1A, DYRK1B, and DYRK2, respectively. This compound induces caspase-3/7-mediated cell apoptosis and reduces CLK-dependent phosphorylation. T025 exhibits anti-proliferative activities in both hematological and solid cancer cell lines with IC50 values ranging from 30-300 nM, making it primarily useful for MYC-driven disease research.
- Orally active and highly potent inhibitor of Cdc2-like kinase (CLKs)
- Induces caspase-3/7-mediated cell apoptosis
- Reduces CLK-dependent phosphorylation
- Exerts anti-proliferative activities in both hematological and solid cancer cell lines
- Anti-tumor efficiency, mainly for MYC-driven disease research
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eMolecules 910232-84-7 | Medchem Express | CGI-1746 | 5mg | 446260482 | HY-11999 | MFCD18782602 | 579.701 | C34H37N5O4
Medchem Express | CGI-1746 | 5mg | 446260482 | HY-11999 | 910232-84-7 | MFCD18782602 | 579.701 | C34H37N5O4
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Cayman Chemical ChloramphenIcol PalmItate 25mg
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An orally bioavailable ester prodrug form of the antibiotic chloramphenicol; is hydrolyzed in the small intestine to release chloramphenicol
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Medchemexpress LLC Cilazapril monohydrate | 92077-78-6 | MFCD00865788 | 99.9% | C22H33N3O6 | 5 MG
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Cilazapril monohydrate is an orally active prodrug of the angiotensin-converting enzyme (ACE) inhibitor Cilazaprilat. It reduces plasma ACE activity and can be used in the research of hypertension (including essential and renal hypertension) and congestive heart failure.
- Orally active prodrug of Cilazaprilat
- Reduces plasma ACE activity
- Applicable in research for hypertension (essential and renal) and congestive heart failure
- Evokes a maximum degree of plasma ACE inhibition (-76%) in rats
- Dose-dependently reduces plasma ACE activity and pressor response to angiotensin in cats
- Gradually reduces blood pressure in dogs with volume-depleted renal hypertension
- Decreases blood pressure, reduces heart weight to body weight ratio, and improves postischemic myocardial function in hyperthyroid rats
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Apexbio Technology LLC Azithromycin Dihydrate 117772-70-0 10mM (in 1mL DMSO)
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Azithromycin Dihydrate (CAS 117772-70-0) is a macrolide antibiotic targeting the bacterial 50S ribosomal subunit It is designed to inhibit bacterial protein synthesis thereby disrupting bacterial growth and replication Azithromycin Dihydrate exerts its biological activity primarily through reversible binding to the 50S ribosomal subunit inhibiting protein synthesis In in vitro assays Azithromycin Dihydrate demonstrates inhibitory activity against susceptible bacterial strains with reported IC50 values typically in the micromolar range Based on these pharmacological properties Azithromycin Dihydrate holds research potential in investigating mechanisms of antibiotic resistance bacterial susceptibility and developing therapeutic strategies against bacterial infections
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eMolecules 74610-55-2 | Medchem Express | Tylosin (tartrate) | 50mg | 446272903 | HY-B0519 | MFCD07783824 | 1066.198 | C50H83NO23
Medchem Express | Tylosin (tartrate) | 50mg | 446272903 | HY-B0519 | 74610-55-2 | MFCD07783824 | 1066.198 | C50H83NO23
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Enzo Life Sciences D-NMMA . monoacetate (25mg). CAS: 137694-75-8
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D-NMMA is inactive as an inhibitor of NOS and may be used to explore non-specific effects of L-NMMA. Alternative name: NG-Monomethyl-D-arginine . monoacetate. Formula: C7H16N4O2 . CH3COOH. MW: 188.2 . 60.1. Purity: ≥99%. Appearance: White solid. Solubility: Soluble in water. Long Term Storage: +4°C.
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Selleck Chemical LLC Erythromycin Ethylsuccinate S4060-50mg
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Erythromycin Ethylsuccinate an oral macrolide antibiotic produced by Streptomyces erythreus reversibly binds to the 50S ribosome of bacteria and inhibits protein synthesis
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Medchemexpress LLC Poloxin Solid Solvent | HY-12134
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Poloxin Solid Solvent
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Invivogen ZEOCIN SOLUTION 500MG
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ZEOCIN SOLUTION 500MG ..
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Medchemexpress LLC BRD3731 (S enantiomer) | 2056262-07-6 | 98.2% | 377.52 g/mol | C24H31N3O | 100MG
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BRD3731 (S-enantiomer) is a selective GSK3β inhibitor supplied for preclinical biochemical and cell-based research. It has been reported as a GSK3β-selective compound (from patent US20160375006A1) and is used in studies of mood disorders, metabolic disease, and neurodegeneration. The compound is provided as a solid or as DMSO solution formats and is characterized by defined physicochemical properties and high purity.
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Medchemexpress LLC IRAK4-IN-4 50mg | 1850276-58-2 | 50 MG
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IRAK4-IN-4 is a research small-molecule inhibitor of interleukin-1 receptor-associated kinase 4 (IRAK4) with additional activity against cyclic GMP-AMP synthase (cGAS). Supplied as a light yellow solid with reported high purity, it is used in biochemical and cellular studies to probe IRAK4- and cGAS-mediated signaling pathways in inflammation and autoimmune disease research.
- Potent IRAK4 inhibition (IC50 2.8 nM).
- Potent cGAS inhibition (IC50 2.1 nM).
- High purity (99.6%).
- Light yellow solid physical form.
- Molecular weight 340.37 g/mol.
- Suitable for preclinical biochemical and cellular assays.
- Available in multiple small milligram pack sizes for research use.
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