Cell Culture Media, Supplements, and Reagents
Medchemexpress LLC Hzx-02-059 (Compound 13) | 2240205-30-3 | 99.4% | 487.48 g·mol⁻¹ | C27H20F3N5O | 5 MG
HZX-02-059 is a small-molecule research compound that induces methuosis and functions as a dual PIKfyve/tubulin inhibitor with reported anticancer activity. It disrupts endocytosis-exocytosis balance to produce extensive intracellular vacuolization and promotes cell death pathways, including apoptosis; reported signaling effects include inhibition of PI3K/AKT phosphorylation and suppression of c-Myc and NF-κB transcription.
- Induces methuosis and intracellular vacuolization.
- Dual PIKfyve and tubulin inhibitory activity.
- Promotes apoptosis and cell death in cellular models.
- Modulates PI3K/AKT, c-Myc, and NF-κB signaling.
- Supplied as a high-purity small molecule for cellular assays.
- Molecular formula C27H20F3N5O; molecular weight 487.48 g·mol⁻¹.
Miltenyi Biotec, Inc. MACS GMP Recombinant Human IL-7 (100 µg)
Recombinant human interleukin 7.
This product is subject to the following: Miltenyi Biotec, Inc. Terms and Conditions of Sale For Products and Services
Medchemexpress LLC Sri-011381 | 1629138-41-5 | MFCD01475985 | 99.6% | 329.48 g/mol | C20H31N3O | 50 MG
SRI-011381 is a small-molecule agonist of the TGF-β/Smad signaling pathway with reported neuroprotective effects. It is provided as a research-use chemical in powder and solution formats for in vitro and in vivo studies.
- Orally active TGF-β/Smad signaling agonist
- Reported neuroprotective effects in preclinical studies
- Molecular formula C20H31N3O; molecular weight 329.48 g/mol
- CAS number 1629138-41-5
- High purity (~99.6%)
- Available as dry powder and as 10 mM solution in DMSO
- Store at 4°C protected from light; in solvent store at -80°C (6 months) or -20°C (1 month)
Medchemexpress LLC Lenampicillin hydrochloride | 80734-02-7 | MFCD01745174 | >99.0% | 497.95 | C21H24ClN3O7S | 10 MG
Lenampicillin hydrochloride is an orally active prodrug of ampicillin used as a research reagent. As a beta-lactam antibacterial, it exhibits improved oral absorption and reduced adverse effects compared with ampicillin and is commonly used in studies of suppurative skin and soft tissue infections.
- Orally active prodrug of ampicillin.
- Improved absorption and reduced side effects compared with ampicillin.
- Beta-lactam antibacterial that inhibits penicillin-binding proteins.
- Supplied as the hydrochloride salt for enhanced solubility.
- Suitable for in vitro and in vivo research on suppurative infections.
- Available in small research pack sizes.
Miltenyi Biotec, Inc. CryoMACS Freezing Bag 1000
The bags are intended for a single cycle of freezing, storage (down to -196°C), and subsequent thawing (at +37°C) of hematopoietic progenitor cells (recommended fill volume 125-270 mL).
This product is subject to the following: Miltenyi Biotec, Inc. Terms and Conditions of Sale For Products and Services
Medchemexpress LLC JH-X-119-01 | 2227368-54-7 | 99.0% | 452.46 g/mol | C25H20N6O3 | 100 MG
JH-X-119-01 is a research-grade, small-molecule inhibitor selective for interleukin-1 receptor-associated kinase 1 (IRAK1) with reported efficacy in an LPS-induced sepsis mouse model. It is provided as a high-purity powder for preclinical cellular and in vivo studies.
- Potent and selective IRAK1 inhibition for signaling studies.
- Demonstrated activity in LPS-induced sepsis in mice.
- High reported purity suitable for biochemical assays and animal work.
- Available in multiple powder package sizes to suit experiment scale.
- Stable with recommended cold storage for long-term use.
Medchemexpress LLC 2,2'-(1,4-phenylene)bis(4,5-diphenyl-1H-imidazole) | 4051-59-6 | 98.0% | 514.62 g/mol | C36H26N4 | 10 MG
MSX-130 is a small-molecule antagonist of the C-X-C chemokine receptor 4 (CXCR4) used in research to inhibit CXCR4-mediated signaling and reduce cancer metastasis. It is supplied as a solid research reagent with defined storage and solubility recommendations suitable for in vitro and in vivo studies.
- Small-molecule CXCR4 antagonist for research applications.
- High purity (98.0%) suitable for biochemical assays.
- Soluble in DMSO (≈2 mg/mL with warming or sonication).
- Stable as powder when stored at recommended temperatures.
- Available in common research package sizes for dose-response work.
Medchemexpress LLC Sri-011381 | 1629138-41-5 | 99.4% | 329.48 g/mol | C20H31N3O | 5 MG
SRI-011381 is an orally active small-molecule agonist of the TGF-β/Smad signaling pathway with reported neuroprotective effects in preclinical studies. It is provided for research use in both solid and solution forms and is commonly used to probe TGF-β pathway activation in vitro and in vivo.
- Orally active TGF-β/Smad signaling agonist.
- Exhibits reported neuroprotective effects in preclinical models.
- High reported purity (99.4%).
- Molecular weight 329.48 g/mol.
- Chemical formula C20H31N3O.
- Available as multiple solid sizes and as a 10 mM solution in DMSO.
- Suitable for in vitro and in vivo pathway activation studies.
![Medchemexpress LLC 1-cyano-3-(4-cyanophenyl)-2-[(2R)-3,3-dimethylbutan-2-yl]guanidine | 220641-11-2 | MFCD30747839 | 99.6% | 269.34 g/mol | C15H19N5 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000214212.png-250.jpg)
Medchemexpress LLC 1-cyano-3-(4-cyanophenyl)-2-[(2R)-3,3-dimethylbutan-2-yl]guanidine | 220641-11-2 | MFCD30747839 | 99.6% | 269.34 g/mol | C15H19N5 | 50 MG
Naminidil is a cyanoguanidine small molecule that acts as an ATP-sensitive potassium (KATP) channel opener. It is provided as a research-grade reagent for in vitro and in vivo pharmacological studies of potassium channel function and cardiovascular mechanisms. The compound has molecular formula C15H19N5, molecular weight 269.34 g/mol, and reported CAS number 220641-11-2.
- Acts as an ATP-sensitive potassium (KATP) channel opener for functional studies.
- High purity (about 99.6%) suitable for research applications.
- Available in multiple pack sizes including 50 mg for flexible dosing.
- Characterized molecular properties (C15H19N5; MW 269.34 g/mol).
- Provided with analytical documentation such as COA and SDS for safety and quality assurance.
Medchemexpress LLC Lenampicillin hydrochloride | 80734-02-7 | 99.0% | 497.95 g/mol | C21H24ClN3O7S | 5 MG
Lenampicillin hydrochloride is the hydrochloride salt of lenampicillin, an orally active prodrug of ampicillin. It acts as a beta-lactam antibacterial that inhibits bacterial penicillin-binding proteins and is commonly used in research on suppurative skin and soft tissue infections.
- Orally active prodrug enabling systemic absorption.
- Beta-lactam mechanism inhibiting penicillin-binding proteins.
- Improved absorption and reduced side effects compared with ampicillin.
- Suitable for antibacterial activity and pharmacokinetic research.
- Supplied as a high-purity research reagent for laboratory use.
![Medchemexpress LLC 2-methyl-N-[(1S)-2-(methylphenylamino)-2-oxo-1-(phenylmethyl)ethyl]-1H-indole-3-acetamide | 1352879-65-2 | 98.9% | 5MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000234274.png-250.jpg)
Medchemexpress LLC 2-methyl-N-[(1S)-2-(methylphenylamino)-2-oxo-1-(phenylmethyl)ethyl]-1H-indole-3-acetamide | 1352879-65-2 | 98.9% | 5MG
2-methyl-N-[(1S)-2-(methylphenylamino)-2-oxo-1-(phenylmethyl)ethyl]-1H-indole-3-acetamide | 1352879-65-2 | 98.9% | 5MG
Medchemexpress LLC Bay-850 | 2099142-76-2 | 98.3% | 100 MG
Bay-850 is a small-molecule chemical probe that selectively inhibits ATPase family AAA domain-containing protein 2 (ATAD2). It is characterized as a potent, isoform-selective ATAD2 inhibitor (IC50 166 nM) used in biochemical and cell-based studies to probe ATAD2 function, disrupt ATAD2-chromatin interactions, and induce bromodomain dimerization.
- Potent, isoform-selective ATAD2 inhibition (IC50 166 nM).
- Induces ATAD2 bromodomain dimerization and disrupts ATAD2-chromatin interaction.
- High purity suitable for biochemical assays (98.3% by HPLC).
- Powder form, readily soluble in DMSO for stock solutions.
- Molecular weight 654.24 g/mol; formula C38H44ClN5O3.
- Available with COA and RP-HPLC report for analytical verification.
Medchemexpress LLC IRAK4-IN-4 25mg | 1850276-58-2 | 25 MG
IRAK4-IN-4 is a research-grade small-molecule inhibitor of interleukin-1 receptor-associated kinase 4 (IRAK4) with demonstrated potency in enzymatic assays.
- Potent IRAK4 inhibitor (IC50 = 2.8 nM).
- Inhibits cyclic GMP-AMP synthase (cGAS) with IC50 = 2.1 nM.
- High purity (99.55%).
- Molecular formula C22H16N2O2; molecular weight 340.37.
- Light yellow to yellow solid supplied in milligram quantities.
- Recommended storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (2 years) or -20°C (1 year).
Medchemexpress LLC Wyc-210 (tazarotene derivative) | 2131803-93-3 | 99.2% | 340.40 | C18H16N2O3S | 5 MG
WYC-210 is a tazarotene-derivative small-molecule retinoid intended for research use. The compound contains an alkyne functional group and is used as a click-chemistry reagent; it has been reported to exhibit relatively low anticancer activity. The material is supplied with a high purity specification and explicit storage recommendations for solid and solution forms.
- Contains an alkyne group suitable for click chemistry.
- Tazarotene-derived retinoid scaffold.
- High reported purity, suitable for analytical and synthetic applications.
- Available in small-mass packages for laboratory-scale experiments.
- Recommended storage conditions specified for powder and solutions.