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Filtered Search Results
TARGETMOL CHEMICALS INC GLP-17-37 ACETATE106612- 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Glp-1(7-37) acetate is an intestinal insulin hormone that enhances glucose-induced insulin secretion. purity: 98%
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Apexbio Technology LLC APEXBIO TECHNOLOGY LLC
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5000569606 MIDECAMYCIN-200MG
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TARGETMOL CHEMICALS INC CP-466722 10MG
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Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. CP-466722 an effective and reversible ATM inhibitor does not inhibit ATR and PI3K or PIKK family members in cells. purity: 99%
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![Medchemexpress LLC Naphtho[1,2-d]thiazol-2-ylamine | 40172-65-4 | MFCD00051329 | 99.7% | 200.27 | C11H8N2S | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000264707.png-250.jpg)
Medchemexpress LLC Naphtho[1,2-d]thiazol-2-ylamine | 40172-65-4 | MFCD00051329 | 99.7% | 200.27 | C11H8N2S | 5 MG
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SKA-31 (Naphtho[1,2-d]thiazol-2-ylamine, CAS 40172-65-4) is a research-grade small-molecule activator of calcium-activated potassium channels (KCa2/KCa3.1), used to probe ion channel function and endothelial or neuronal hyperpolarization in vitro and in vivo studies.
- Potent channel activator with KCa3.1 EC50 ~260 nM and KCa2 subtype EC50s in the low micromolar range.
- High purity for research use (≈99.7%).
- Small molecular weight and defined composition: 200.27 g/mol; formula C11H8N2S.
- Soluble in DMSO (≈125 mg/mL) and formulatable for in vivo dosing.
- Supplied as a solid powder suitable for biochemical and cellular assays.
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Medchemexpress LLC 3,6,9,12,15,18-Hexaoxaeicosane-1,20-diamine | 76927-70-3 | ≥97.0% | 324.41 | 1 G
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Amino-PEG6-amine is a PEG-based (6 units) PROTAC linker that can be utilized in the synthesis of PROTACs. It is intended for research use only.
- PEG-based (6 units) PROTAC linker
- Can be used in the synthesis of PROTACs
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Chemscene CHEMSCENE
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5000579831 EEDQ 25G
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Chemscene CHEMSCENE
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5000579991 8-BROMOQUINOLINE 5G
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Medchemexpress LLC Letrozole (Standard) | 112809-51-5 | C17H11N5 | 200 MG
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Letrozole (CGS 20267) is a potent, selective, reversible, and orally active non-steroidal inhibitor of aromatase, with an IC50 of 11.5 nM. It selectively inhibits estrogen biosynthesis and can be used for breast cancer research.
- Potent, selective, reversible, and orally active non-steroidal inhibitor of aromatase
- Selectively inhibits estrogen biosynthesis
- Used for breast cancer research
- Exhibits anti-tumor effects in rats
- Inhibits growth of MCF-7 epithelial breast cancer cells
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Medchemexpress LLC Isavuconazole | 241479-67-4 | 99.9% | C22H17F2N5OS | 200 MG
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Isavuconazole is a triazole proagent that exhibits antifungal activity against yeasts, molds, and dimorphic fungi. It functions by inhibiting ergosterol biosynthesis, which leads to the disruption of the fungal membrane structure and function. Isavuconazole is also identified as a moderate inhibitor of CYP3A4.
- Triazole proagent
- Exhibits antifungal activity against yeasts, molds, and dimorphic fungi
- Inhibits ergosterol biosynthesis
- Disrupts fungal membrane structure and function
- Moderate inhibitor of CYP3A4
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Medchemexpress LLC Trifluoperazine dihydrochloride | 440-17-5 | MFCD00012656 | 99.9% | 500 MG
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Trifluoperazine dihydrochloride is an antipsychotic agent that functions by blocking central dopamine receptors. It is also a potent α1-adrenergic receptor antagonist and a potent NUPR1 inhibitor, exhibiting anticancer activity. Additionally, it acts as a calmodulin inhibitor and inhibits P-glycoprotein. This compound can be used in schizophrenia research and is a reversible inhibitor of influenza virus morphogenesis.
- Antipsychotic agent
- Blocks central dopamine receptors
- Potent α1-adrenergic receptor antagonist
- Potent NUPR1 inhibitor
- Exerts anticancer activity
- Calmodulin inhibitor
- Inhibits P-glycoprotein
- Used for schizophrenia research
- Reversible inhibitor of influenza virus morphogenesis
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Medchemexpress LLC Alimemazine hemitartrate | 4330-99-8 | 98.4% | 200 MG
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Alimemazine hemitartrate is an antagonist of the histamine (HA) receptor that also acts as a partial agonist at other GPCR receptors. This compound exhibits anti-serotonin, antispasmodic, antihistamine, sedation, hypnotic, antiviral, and anti-nausea properties. It promotes pancreatic β-cell growth and improves diabetes in mice. This product is intended for research use only.
- Acts as a histamine (HA) receptor antagonist
- Functions as a partial agonist at GPCR receptors
- Exhibits anti-serotonin, antispasmodic, and antihistamine properties
- Offers sedative, hypnotic, antiviral, and anti-nausea effects
- Promotes pancreatic β-cell growth
- Improves diabetes in mouse models
- Reduces SARS-CoV-2 induced syncytia formation
- Inhibits SARS-CoV-2 in HEK293T/ACE2 and VeroE6/TMPRSS2 cells
- For research use only
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Medchemexpress LLC Azido-PEG8-amine | 857891-82-8 | >99.9% | C18H38N4O8 | 100 MG
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Azido-PEG8-amine is a PEG-based PROTAC linker designed for the synthesis of PROTACs. It features an azide group that enables its use as a click chemistry reagent for various bioconjugation strategies.
- Functions as a click chemistry reagent
- Participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne groups
- Engages in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups
- Utilized in the synthesis of PROTACs for targeted protein degradation
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eMolecules Ambeed / 4-Hydroxyquinoline-3-carboxylic acid / 1g / 552554610 / A125405 / / 34785-11-0 / MFCD00598887 / 189.170 / C10H7NO3
Ambeed / 4-Hydroxyquinoline-3-carboxylic acid / 1g / 552554610 / A125405 / / 34785-11-0 / MFCD00598887 / 189.170 / C10H7NO3
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Apexbio Technology LLC APEXBIO TECHNOLOGY LLC
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5000569271 RHEIN-200MG
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Medchemexpress LLC Lodoxamide (U-42585E free acid) | 53882-12-5 | 98.1% | C11H6ClN3O6 | 200 MG
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Lodoxamide (U-42585E free acid) is an antiallergic compound that acts as a mast-cell stabilizer, used for the treatment of asthma and allergic conjunctivitis.
- Inhibits histamine release and calcium influx in mast cells.
- Reduces chemotactic response of eosinophils to fMLP and IL-5.
- Inhibits eosinophil peroxidase release after IgA-dependent activation.
- Demonstrates cromolyn-like activity in mast cell assays and antigen-sensitized rhesus monkeys.
- Inhibits increased respiratory frequency and decreased tidal volume induced by antigen challenge.
- Reduces lung reperfusion injury in organ preservation solutions.
- Improves daytime breathing difficulty, cough, sputum, and sleep in patients.
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