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Filtered Search Results
Cell Signaling Technology CHIR-99021, GSK-3 Inhibitor, Lyophilized Powder, 5 mg
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CHIR-99021 is a potent and highly selective inhibitor of glycogen synthase kinase-3β (GSK-3β) and GSK-3α with IC50 values of 6.7 and 10 nM, respectively. By demonstrating >500-fold selectivity for GSK-3 over 20 other protein kinases, this compound is valuable for researching pathways involved in type 1 and type 2 diabetes, where it has been shown to increase beta cell replication in isolated rat islets.
- Potent inhibition of GSK-3β and GSK-3α
- High selectivity (>500-fold) for GSK-3
- Supports research into beta cell replication
- Supplied as a lyophilized powder
- Easy reconstitution in DMSO for a 10 mM stock
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Cell Signaling Technology Hydroxychloroquine Sulfate, >98% Purity, 50 mg
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Hydroxychloroquine Sulfate is a 4-aminoquinoline derivative of quinine that acts as an anti-malaria drug and immunomodulatory agent. It is utilized in studies of rheumatoid arthritis, systemic lupus erythematosus, and various rheumatic diseases due to its ability to inhibit lysosome and autophagosome functions, interfere with cytokine production, and disrupt cGAS/dsDNA complexes to inhibit IFN-β production. The compound also demonstrates antiviral and anti-inflammatory effects, including inhibition of SARS-CoV-2 infection in vitro.
- Supplied as a lyophilized powder
- Inhibits IFN-β production with an IC50 of 25 μM
- Modulates metabolic, cardiovascular, antithrombotic, and antineoplastic pathways
- For a 10 mM stock, reconstitute 5 mg of powder in 1.15 mL of water
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Cell Signaling Technology U-18666A, Cholesterol Transport Inhibitor, 5 mg
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U-18666A is a cell-permeable small molecule that functions as a potent inhibitor of intracellular cholesterol transport. By blocking low-density lipoprotein (LDL)-derived cholesterol trafficking, this compound prevents cholesterol esterification and suppresses LDL receptor activity. It is widely utilized in research to simulate intracellular cholesterol accumulation, providing a valuable tool for investigating the pathogenesis of neurological disorders, such as Alzheimer™ disease and Niemann-Pick disease type C, as well as atherosclerosis and viral infection mechanisms.
- Inhibits LDL-derived cholesterol transport and esterification
- Suppresses LDL receptor activities
- Useful for studying intracellular cholesterol accumulation and neurodegenerative pathologies
- Relevant for research on viral entry and replication
- Supplied as a lyophilized powder
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Cell Signaling Technology Poly(I:C) Sodium Salt, Lyophilized, >98% Purity, 25 mg
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Poly(I:C) Sodium Salt is a synthetic analog to double-stranded RNA (dsRNA) and a potent activator of Toll-like receptor 3 (TLR3). It plays a significant role in the innate immune response by mimicking viral infection to trigger the activation of transcription factors NF-κB and IRF3. This reagent is intended for research use.
- Acts as a potent TLR3 agonist
- Supplied as a lyophilized powder
- Purity of >98%
- Soluble in water at 10 mg/mL with warming
- Compatible with use in studies investigating vaccine immunogenicity
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Medchemexpress LLC Oxyphenbutazone monohydrate | 7081-38-1 | 98.0% | 50 MG
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Oxyphenbutazone monohydrate is a metabolite with anti-inflammatory effects. It acts as an orally active non-selective COX inhibitor and can selectively eliminate non-replicating Mycobacterium tuberculosis.
- Anti-inflammatory effect.
- Orally active.
- Non-selective COX inhibitor.
- Selectively kills non-replicating Mycobacterium tuberculosis.
- Enhances anticancer efficiency in certain cells.
- Exhibits reparative effects in hepatocytes.
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AdipoGen Geodin (5 mg)
Chemical. CAS: 427-63-4. Formula: C17H12Cl2O7. MW: 399.2. Isolated from Penicillium sp. FKI-5002. Plasminogen activator inhibitor (PAI-1). Glucose uptake stimulator.
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AdipoGen DAF-4T (1 mg)
Chemical. CAS: 212558-80-0. Formula: C20H7O5N3Cl2. MW: 440.19. Fluorescent reference compound for DAF-4 DA (CDX-D0216). Spectral data: lambdaEx=505nm; lambdaEm=530nm.
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AdipoGen DAF-4T (5 mg)
Chemical. CAS: 212558-80-0. Formula: C20H7O5N3Cl2. MW: 440.19. Fluorescent reference compound for DAF-4 DA (CDX-D0216). Spectral data: lambdaEx=505nm; lambdaEm=530nm.
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Cayman Chemical HT-2 Toxin, Purity: ≥98%, CAS: 26934-87-2, 5 mg
A mycotoxin and an active metabolite of T-2 toxin; reduces viability of a variety of cancer cells (IC50s = 3.1-23 ng/ml) and HUVECs (IC50 = 56.4 ng/ml); induces oxidative stress, DNA damage, and autophagy in, as well as halts the development of, cultured mouse embryos at 10 nM
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Selleck Chemical LLC Enfortumab vedotin-ejfv-1MG-5
Enfortumab vedotin-ejfv (Padcev) is an antibody-drug conjugate (ADC) composed of an fully human anti-Nectin-4 IgG1 kappa monoclonal antibody (AGS-22C3) conjugated to Monomethyl Auristatin E (MMAE) via a protease-cleavable maleimidocaproyl-valyl-citrullinyl-p-aminobenzyloxycarbonyl Enfortumab vedotin-ejfv has the potential for use in research of urothelial carcinoma
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Cayman Chemical Proscaline (hydrochloride), Purity: ≥98%, CAS: 61367-69-9, 5 mg
An analytical reference standard categorized as a phenethylamine; intended for research and forensic applications
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Medchemexpress LLC MK-4166 5mg | 5mg
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MK-4166 is a humanized IgG1 agonist monoclonal antibody targeting GITR MK-4166 enhances the proliferation of both na ve and tumor-infiltrating T lymphocytes[1]
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Active Motif GSK-J4 (cell permeable)
Active Motif's GSK-J4 is an inhibitor of the histone demethylase JMJD3/UTX. It inhibits demethylation of histone H3K27. GSK-J4 reduces LPS-induced proinflammatory cytokine production in primary human macrophages (IC50 = 9 uM for the inhibition of TNF-alpha release). It is a cell permeable, ethyl ester of GSK-J1 (Catalog No. 14068). GSK-J4 rescues newborn pups from embryonic lethality in BRAF knockin mice which recapitulate major features of RASopathies.
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Medchemexpress LLC Antineoplaston A10 | 91531-30-5 | 99.8% | 100 MG
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Antineoplaston A10 is an antineoplaston that inhibits the growth of human hepatoma cells by inducing apoptosis. It is for research use only and can be used in the study of liver cancer and breast cancer.
- Inhibits the growth of human hepatoma cell lines HepG2 and HLE
- Induces apoptosis
- Targets Ras
- Reduces bcl-2 expression in cytoplasm
- Increases nuclear p53 expression
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Medchemexpress LLC 1-Boc-homopiperazine | 112275-50-0 | 99.87% | 200.28 | 50 G
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1-Boc-homopiperazine is a drug intermediate used for the synthesis of bacterial FtsZ inhibitors. It is a colorless to light yellow liquid for research use only.
- Used for the synthesis of bacterial FtsZ inhibitors
- Colorless to light yellow liquid appearance
- High purity of 99.87%
- Molecular weight of 200.28
- Recommended storage at 4°C, protected from light
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