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Filtered Search Results
Medchemexpress LLC Clopyralid | 1702-17-6 | MFCD00078655 | 98.5% | 192.00 | C6H3Cl2NO2 | 100 G
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Clopyralid is a selective pyridine-carboxylic herbicide (CAS 1702-17-6) supplied as a research-grade chemical for study and formulation development. It is used to control broadleaf weeds, including thistles and clovers, and is noted for its persistence in soils; users should follow handling and safety guidance in the SDS.
- Selective control of broadleaf weeds.
- High purity suitable for research (98.5%).
- Defined chemical identity: C6H3Cl2NO2, MW 192.00.
- Available in multiple laboratory pack sizes.
- Documentation available including SDS, COA, and datasheet.
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Apexbio Technology LLC Sodium Monofluorophosphate 10163-15-2 10mM (in 1mL H20)
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Sodium Monofluorophosphate is a small-molecule inhibitor targeting enzymes including pyruvate kinase alkaline phosphatase and phosphorylase phosphatase It is designed to competitively and irreversibly inhibit these enzymes thereby modulating enzyme-mediated phosphorylation processes and impacting glycogen metabolism pathways Sodium Monofluorophosphate exerts its biological activity primarily through competitive inhibition of pyruvate kinase and alkaline phosphatase by interfering with endogenous phosphate substrates and irreversible inhibition of phosphorylase phosphatase Based on these pharmacological properties Sodium Monofluorophosphate holds research potential in the study of enzymatic mechanisms involving phosphate-transfer reactions and in investigations of metabolic regulations dependent on pyruvate kinase alkaline phosphatase and phosphorylase phosphatase pathways
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Medchemexpress LLC Slingshot inhibitor D3 | 1715076-35-9 | 99.5% | 461.55 g·mol⁻¹ | C25H19NO4S2 | 10MM 1ML
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Slingshot inhibitor D3 is a potent, selective, reversible, and competitive inhibitor of Slingshot phosphatases (SSH family) used in biochemical and cell-based assays to probe SSH function. It is supplied as a ready-to-use 10 mM solution in DMSO and is intended for inhibition studies, mechanistic assays, and compound screening.
- Potent inhibition of Slingshot 1 (IC50 = 3 μM) and activity against Slingshot 2 (Ki = 3.9 μM).
- Supplied as a 10 mM solution in DMSO, 1 mL vial ready for use.
- High purity (~99.5%) suitable for research applications.
- Molecular weight 461.55 g·mol⁻¹ and formula C25H19NO4S2.
- Useful for biochemical and cell-based assays to study Slingshot-mediated dephosphorylation pathways.
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Apexbio Technology LLC Butenafine HCl 101827-46-7 10mM (in 1mL DMSO)
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Butenafine HCl (CAS 101827-46-7) is a small-molecule inhibitor targeting squalene epoxidase It is designed to inhibit this enzyme thereby disrupting fungal sterol biosynthesis Butenafine HCl exerts its biological activity primarily through inhibition of squalene epoxidase leading to impaired ergosterol synthesis and accumulation of squalene which disrupts fungal cell membrane integrity and results in cell death In biochemical studies Butenafine HCl demonstrates inhibitory activity with reported IC50 values ranging from approximately 0 03 M to 0 1 M depending on fungal species and experimental conditions Based on these pharmacological properties Butenafine HCl holds research potential in biomedical antifungal studies including investigations into fungal physiology antifungal efficacy and drug resistance mechanisms
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Medchemexpress LLC Polyethylene glycol 20000 | 25322-68-3 | 20000.00 Da | H(OCH2CH2)nOH | 250g
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PEG20000 (Polyethylene glycol 20000) can be used as a solubilizer PEG20000 is a kind of biological materials or organic compounds that are widely used in life science research can be degraded by bacteria[1][2]
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Medchemexpress LLC Polyethylene glycol 3000 | 25322-68-3 | 98.0% | 3000.00 g/mol | H(OCH2CH2)nOH | 100g
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PEG3000 (Polyethylene glycol 3000) is a solvent for a large number of substances PEG3000 can be used as a carrier material and modifying agent PEG3000 is widely used in a variety of pharmaceutical formulations[1]
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Apexbio Technology LLC Tizanidine HCl 64461-82-1 10mM (in 1mL DMSO)
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Tizanidine hydrochloride (CAS 64461-82-1) is a small molecule that functions as an agonist at 2-adrenergic receptors By activating these presynaptic receptors it suppresses the release of neurotransmitters from central noradrenergic neurons thereby modulating synaptic transmission in the central nervous system This mechanism makes Tizanidine HCl a valuable tool for investigating 2-adrenergic signaling pathways neurotransmitter regulation and CNS synaptic function in biomedical research settings
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Medchemexpress LLC Benzeneacetamide, N-[(1R)-4-[(aminoiminomethyl)amino]-1-[[1R)-1-(4-hydroxyphenyl)ethyl]amino] | 00-00-0 | MFCD04112988 | 99.7% | 533.62 g/mol | C29H35N5O5 | 50 MG
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Y1 receptor antagonist 1 formic is a small-molecule research compound that selectively inhibits the neuropeptide Y (NPY) Y1 receptor. It is provided as a purified formic salt and is intended for in vitro pharmacology and receptor-signaling studies, with analytical characterization for identity and purity.
- Selective Y1 receptor antagonism suitable for receptor pharmacology studies.
- High purity as confirmed by HPLC for consistent experimental results.
- Supplied as a formic salt to aid solubility in polar solvents.
- Characterized by molecular formula C29H35N5O5 and molecular weight 533.62 g/mol.
- Intended for research use only; not for human or clinical use.
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Medchemexpress LLC Tetrahexylammonium iodide | 2138-24-1 | MFCD00041981 | ≥99.0% | 481.58 g/mol | C24H52IN | 25 G
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Tetrahexylammonium iodide is a quaternary ammonium salt used as a reagent in organic synthesis and biochemical assays. It is commonly employed where tetraalkylammonium salts are required for phase-transfer catalysis, ion pairing, or as electrolyte components. Consult the product data sheet and SDS for handling, storage, and safety information.
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Medchemexpress LLC Probenecid sodium | 23795-03-1 | MFCD01661360 | 99.4% | 307.34 | C13H18NNaO4S | 25 G
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Probenecid sodium is the sodium salt of probenecid used in cell biology and pharmacology research as a selective TRPV2 agonist and an inhibitor of pannexin 1 channels. It is supplied as a high-purity research reagent with defined molecular properties and storage recommendations for stability.
- Acts as a selective TRPV2 agonist and pannexin 1 inhibitor.
- High purity (reported 99.4%).
- Available in laboratory-scale package sizes, including 25 G.
- Chemical formula C13H18NNaO4S; molecular weight 307.34 g/mol.
- Recommended to store sealed and away from moisture; long-term stability in solvent at -80°C.
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Medchemexpress LLC N-benzylaniline (N-phenylbenzylamine) | 103-32-2 | MFCD00003018 | 99.9% | 183.25 g/mol | C13H13N | 25 G
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N-Benzylaniline (N-phenylbenzylamine) is an N-alkylated derivative of aniline commonly used as a research chemical and synthetic intermediate in organic and medicinal chemistry. It is supplied as a high-purity material for laboratory research use only and is not intended for human consumption.
- High reported purity suitable for research applications.
- Molecular formula C13H13N; molecular weight 183.25 g/mol.
- Available in multiple pack sizes, including a 25 g solid bottle.
- Soluble in DMSO and offered as a ready-to-use DMSO solution.
- Typical uses include synthetic transformations and analytical reference standards.
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Medchemexpress LLC Cathepsin C/DPPI protein, mouse (inactive, His-Myc) | >95.0% | 250UG
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Recombinant inactive mouse Cathepsin C/DPPI protein fragment expressed in E. coli and supplied lyophilized with N-terminal 10xHis and C-terminal Myc tags. The product corresponds to residues D25-W134, is provided at high purity, and is intended for biochemical, structural, and antibody development applications.
- Inactive recombinant mouse Cathepsin C fragment for nonenzymatic studies.
- N-terminal 10xHis and C-terminal Myc tags for detection and purification.
- >95.0% purity by reducing SDS-PAGE.
- Lyophilized from 10 mM Tris-HCl, 1 mM EDTA, 6% trehalose (pH 8.0).
- Stable when stored lyophilized at -20°C; reconstituted stability: 4°C for 1 week or -20°C with carrier.
- Approximate molecular weight 16-20 kDa.
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Medchemexpress LLC Enfortumab vedotin-ejfv (solution) | 1346452-25-2 | 152,000 (average) | 1 MG
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Enfortumab vedotin-ejfv is an antibody-drug conjugate (ADC) for research use that targets Nectin-4. It consists of a humanized IgG1 antibody linked to the cytotoxic agent monomethyl auristatin E (MMAE) via a protease-cleavable valine-citrulline linker and is provided as a solution in a 1 mg pack for laboratory studies.
- Targets nectin-4 with a humanized IgG1 antibody.
- Conjugated to MMAE via a valine-citrulline (Val-Cit) protease-cleavable linker.
- Provided as a solution suitable for in vitro research applications.
- Supplied in a 1 mg pack size for laboratory experiments.
- Includes a product data sheet with handling and composition details.
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Medchemexpress LLC GM-CSF protein, human (CHO) | >95.0% | 2UG
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Recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF) produced in Chinese hamster ovary (CHO) cells and supplied lyophilized for research use. It is a hematopoietic growth factor for cell proliferation and functional assays, with high purity and potent activity in TF-1 cell assays.
- Expressed in CHO cells, untagged.
- Purity greater than 95% by reducing SDS-PAGE.
- High biological activity; ED50 <0.2 ng/mL in TF-1 assays.
- Observed glycosylated molecular weight ~17-32 kDa.
- Lyophilized formulation with trehalose for stability.
- Stable at -20°C; aliquot and store at -80°C for extended storage.
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Medchemexpress LLC Animal-Free CNTF Mo 2ug
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CNTF is a pluripotent neurotrophic factor belonging to the IL-6 cytokine family[1] CNTF could protect retinal cone and rod photoreceptors[2] CNTF has neuroprotective effects on a variety of central and also peripheral nervous system neurons[3] Animal-Free CNTF Protein Mouse (His) is produced by E coli (M1-M198)with C-terminal His-tag This product is for cell culture use only
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