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Filtered Search Results
Pickering Laboratories Inc CHEM LITHIUM DILUENT 4X250ML/C
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Lithium Diluent, pH 2.36, case of 4 (250 mL/bottle) Amino Acid Analysis.
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![Medchemexpress LLC N-methyl-N-[(1S)-1-(2-methyl-5-sulfamoylphenyl)ethyl]-2-(2-oxo-2,3-dihydro-1,3-benzoxazol-3-yl)aceta | 797035-11-1 | MFCD09037559 | ≥98.0% | 578.72 g·mol⁻¹ | C31H38N4O5S | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000212514.png-250.jpg)
Medchemexpress LLC N-methyl-N-[(1S)-1-(2-methyl-5-sulfamoylphenyl)ethyl]-2-(2-oxo-2,3-dihydro-1,3-benzoxazol-3-yl)aceta | 797035-11-1 | MFCD09037559 | ≥98.0% | 578.72 g·mol⁻¹ | C31H38N4O5S | 1 ML
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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b-Secretase Inhibitor IV is a potent, cell-active BACE-1 (beta-secretase) inhibitor used in biochemical and cell-based assays to study amyloid precursor protein processing and BACE-1 activity. It demonstrates low nanomolar potency under typical assay conditions and is available as high-purity solid or as concentrated solution formats for experimental flexibility.
- Potent, cell-active BACE-1 inhibitor with low nanomolar IC50.
- Validated for biochemical and cell-based assays.
- High purity for consistent experimental results.
- Available as concentrated solution or solid for flexibility.
- Suitable for studies of amyloid precursor protein processing.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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FREETHINK TECHNOLOGIES INC
NC3977265 ASAPPRIMEGO SALT SOLUTION VIAL
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Medchemexpress LLC Cathepsin G inhibitor I | 429676-93-7 | MFCD28137715 | 98.0% | 620.63 | C36H33N2O6P | 1 ML
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Cathepsin G Inhibitor I is a selective, reversible, competitive, non-peptide inhibitor of the serine protease cathepsin G with reported IC50 53 nM and Ki 63 nM. The compound is supplied in solution and solid forms for use in biochemical and cellular assays requiring cathepsin G inhibition.
- Potent inhibitor of cathepsin G (IC50 53 nM, Ki 63 nM).
- Reversible, competitive, non-peptide mechanism of action.
- Available as a 10 mM solution in DMSO (1 ml) or as solid in multiple pack sizes.
- Molecular formula C36H33N2O6P and molecular weight ~620.63.
- Suitable for biochemical and cellular inhibition assays.
- Batch purity may vary; verify certificate of analysis before use.
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Aqua Solutions KOH IN IPA 0.05N 10L
NC3865442 KOH IN IPA 0.05N 10L
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Medchemexpress LLC Cathepsin G inhibitor I | 429676-93-7 | MFCD28137715 | ≥99.0% | 620.63 g·mol⁻¹ | C36H33N2O6P | 50 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Cathepsin G Inhibitor I is a selective, reversible, competitive, non-peptide inhibitor of cathepsin G used in biochemical and cellular research to probe cathepsin G-mediated processes. It is supplied as a solid and as a DMSO solution and is formulated for assay-ready use.
- Selective, reversible, competitive inhibitor of cathepsin G (IC50 = 53 nM; Ki = 63 nM).
- High purity suitable for research use (≥99.0%).
- Soluble in DMSO at 50 mg/mL with ultrasonic warming for in vitro applications.
- Available as a solid and as a 10 mM solution in DMSO for convenience in assays.
- Storage guidance provided for solid and solution forms to preserve stability.
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Aqua Solutions Potassium Iodide in MeOH/Water (4L)
Potassium Iodide in MeOH/Water (4L)
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Aqua Solutions FERRIC CHLORIDE SOLUTION 250
Ferric Chloride 250g/100ml (apha For Sulfide)
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Aqua Solutions CDTA Titrant 0.00200 Normal NIST Traceable Solution (10L)
CDTA Titrant 0.00200 Normal NIST Traceable Solution (10L)
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Apexbio Technology LLC LDN-212854 1432597-26-6 10mg
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LDN-212854 (CAS 1432597-26-6) is a highly selective inhibitor of the bone morphogenetic protein (BMP) signaling pathway targeting ALK2 with an IC50 of 1 2 nM In kinase assays LDN-212854 demonstrates potent inhibition of constitutively active ALK2 (caALK2 IC50 16 nM) and displays substantially reduced activity against caALK5 (IC50 2 M) indicative of its BMP pathway selectivity over TGF- signaling Compared to caALK1 and caALK3 its inhibitory activity against caALK2 is 6- and 10-fold greater respectively In BMP receptor-transfected C2C12 cell models LDN-212854 preferentially inhibits caALK2-mediated signaling In transgenic models of heterotopic ossification treatment with LDN-212854 reduces ectopic bone formation This compound is a valuable tool for dissecting BMP/ALK2-driven signaling in cellular and in vivo studies
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Chem Service Inc CHEM SERVICE INC
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NC4006179 NALED SOLUTION
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Medchemexpress LLC Bowman-birk inhibitor | 37330-34-0 | 5 MG
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The Bowman-Birk inhibitor is a highly cross-linked protein with seven disulfide bridges. It has spatially distinct domains designed to inhibit both trypsin and chymotrypsin, making it a significant plant protease inhibitor.
- Highly cross-linked protein with seven disulfide bridges
- Distinct domains to inhibit both trypsin and chymotrypsin
- Functions as a plant protease inhibitor
- Exhibits anticarcinogenic properties
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Aqua Solutions Hydrogen Peroxide Solution, 31% w/w, Reagent ACS (500ML)
Hydrogen Peroxide Solution, 31% w/w, Reagent ACS (500ML)
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MILESTONE MEDICAL TECHNOLOGIES JFC SOLUTION 4X1GAL
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NC3361565 JFC SOLUTION 4X1GAL
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Aqua Solutions TCLP Extraction Fluid #1 Prepared to EPA 1311 pH = 4.93 ± 0.05 (20L)
TCLP Extraction Fluid #1 Prepared to EPA 1311 pH = 4.93 ± 0.05 (20L)
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