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Filtered Search Results
Selleck Chemical LLC CA-074 methyl ester
CA-074 methyl ester (CA-074 Me Cathepsin B Inhibitor IV) is a membrane-permeable derivative of CA-074 and acts as an irreversible cathepsin B inhibitor
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Selleck Chemical LLC CA-074 methyl ester
CA-074 methyl ester (CA-074 Me Cathepsin B Inhibitor IV) is a membrane-permeable derivative of CA-074 and acts as an irreversible cathepsin B inhibitor
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Apexbio Technology LLC NB-598 Maleate 155294-62-5 200mg
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NB-598 Maleate is a small-molecule inhibitor targeting squalene epoxidase (SE) an essential enzyme in cholesterol biosynthesis It is designed to inhibit SE thereby disrupting the oxygenation of squalene and affecting downstream synthesis of cholesterol intermediates particularly within farnesol-dependent pathways leading to triglyceride biosynthesis NB-598 Maleate exerts its biological activity primarily through inhibition of squalene epoxidase In mouse pancreatic islet models NB-598 Maleate reduces insulin secretion under both basal and glucose-stimulated conditions Additionally this compound inhibits calcium voltage-dependent (CaV) ion channels in cellular assays Based on these pharmacological properties NB-598 Maleate holds research potential in studying cholesterol biosynthesis pathways lipid metabolism insulin regulation and the physiological role of CaV channels
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Selleck Chemical LLC Prochlorperazine dimaleate salt S4631-500mg
Prochlorperazine dimaleate salt is a dopamine (D2) receptor antagonist
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Medchemexpress LLC Dibutyl maleate | 105-76-0 | 99.2% | 228.28 | 100 G
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Dibutyl maleate, the diester of Maleic Acid, is used as an intermediate in pharmaceutical synthesis. It can also enhance contact sensitization to Fluorescein isothiocyanate in mice.
- Appearance: liquid (density: 0.988 g/cm³)
- Color: colorless to light yellow
- Initial source: plants Polygonaceae Rheum palmatum L.
- Shipping: room temperature in continental US; may vary elsewhere.
- Storage (pure form): -20°C for 3 years, 4°C for 2 years
- Storage (in solvent): -80°C for 6 months, -20°C for 1 month
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Medchemexpress LLC Ciproxifan maleate | 184025-19-2 | C20H22N2O6 | 5 MG
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Ciproxifan maleate is a potent, selective, orally bioavailable, and competitive antagonist of histamine H3-receptor, with an IC50 of 9.2 nM. It displays low apparent affinity at other receptor subtypes and can be used for the research of aging disorders and Alzheimer's disease.
- Purity: 99.68%
- Appearance: Solid
- Color: White to off-white
- Molecular weight: 386.40
- Solubility in DMSO: ≥ 100 mg/mL
- Solubility in H2O: 3.57 mg/mL
- Ships at room temperature in continental US
- Store at 4°C, sealed, away from moisture
- Store in solvent at -80°C for 6 months or -20°C for 1 month
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eMolecules BENZYL PROPIOLATE 1G
5000189018 BENZYL PROPIOLATE 1G
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Medchemexpress LLC HY-105584 50mg Medchemexpress, Tolycaine CAS:3686-58-6 Purity:>98%
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Medchemexpress, HY-105584 50mg Tolycaine CAS:3686-58-6 Tolycaine is a local anaesthetic agent. 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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Medchemexpress LLC Cefcapene pivoxil hydrochloride hydrate | 147816-24-8 | MFCD01682041 | 99.4% | 622.1 g/mol | C23H32ClN5O9S2 | 50 MG
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Cefcapene pivoxil hydrochloride hydrate is the hydrochloride hydrate salt of cefcapene pivoxil, an orally active cephalosporin-class antibiotic prodrug supplied for research use. It is intended for pharmacological and microbiological studies involving cephalosporin prodrugs and is provided in small milligram-scale quantities for laboratory applications.
- Orally active cephalosporin prodrug.
- Hydrochloride hydrate salt form for improved stability.
- High purity (99.4%).
- Molecular weight 622.1 g/mol; chemical formula C23H32ClN5O9S2.
- Available in small milligram pack sizes suitable for research.
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Medchemexpress LLC Cefcapene pivoxil hydrochloride hydrate | 147816-24-8 | MFCD01682041 | 99.4% | 622.11 g/mol | C23H32ClN5O9S2 | 100 MG
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Cefcapene pivoxil hydrochloride hydrate is a cephalosporin-class antibiotic research compound supplied as a hydrochloride hydrate salt. It is used in in vitro and preclinical studies to evaluate antibacterial activity and related pharmacology, and is distributed with supporting quality and safety documentation.
- High reported purity suitable for analytical and research use.
- Provided with data sheet, certificate of analysis, and safety data sheet for traceability and handling.
- Suitable for in vitro antibacterial and pharmacological research applications.
- Available in multiple small pack sizes for laboratory studies.
- Storage and handling information supplied to maintain stability and safety.
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eMolecules EMOLECULES INC
5000471967 METHYL PROPIOLATE 25G
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Medchemexpress LLC Indacaterol maleate (standard) | 753498-25-8 | 99.6% | C28H32N2O7 | 100 MG
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Indacaterol maleate (standard) | 753498-25-8 | 99.6% | C28H32N2O7 | 100 MG
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Medchemexpress LLC Indacaterol maleate | 753498-25-8 | 99.6% | C28H32N2O7 | 50 MG
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Indacaterol maleate (Standard) is the analytical standard of Indacaterol maleate and is intended for research and analytical applications. It is an orally active ultra-long-acting β2 adrenergic receptor (ADRB2) agonist that inhibits NF-κB activity in a β-arrestin2-dependent manner. This helps in preventing further lung damage and improving lung function in COPD.
- Can be used in cardiovascular disease research.
- Commonly used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
- Helps in preventing further lung damage and improving lung function in COPD.
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Medchemexpress LLC BGT226 (maleate) | 1245537-68-1 | MFCD22124895 | 99.9% | 650.60 g/mol | C32H29F3N6O6 | 5 MG
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BGT226 maleate is a small-molecule PI3K/mTOR dual inhibitor used for research into PI3K signaling and oncology. It shows low-nanomolar potency against PI3K isoforms and mTOR and is used in cell-based and preclinical studies to evaluate antiproliferative and apoptotic effects.
- Inhibits PI3Kα, PI3Kβ, PI3Kγ, and mTOR.
- Exhibits low nanomolar potency in enzymatic assays.
- Demonstrates growth-inhibitory activity in cancer cell models.
- Supplied as the maleate salt for stability.
- High purity suitable for biochemical and cellular assays.
- Available in multiple small pack sizes for research use.
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Medchemexpress LLC 6-[2-(2,4-difluorophenoxy)-5-(ethylsulfonylmethyl)-3-pyridinyl]-8-methyl-2H-pyrrolo[1,2-a]pyrazin-1-on | 2411226-02-1 | 99.9% | 459.47 g·mol⁻¹ | C22H19F2N3O4S | 5 MG
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BET bromodomain inhibitor 1 is a selective, orally active inhibitor of bromodomain and extra-terminal (BET) proteins with potent activity against BRD4 (IC50 = 2.6 nM). Supplied as a white to off-white solid with high purity, it is used in epigenetic target validation and anticancer mechanism research.
- Potent BRD4 inhibition (IC50 2.6 nM).
- Low-nanomolar binding to BET family bromodomains.
- High purity suitable for research (99.9%).
- Soluble in DMSO at 100 mg/mL with warming and sonication.
- Stable when stored as a powder at -20°C for long-term storage.
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