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Filtered Search Results
Selleck Chemical LLC LDN-192960 S3406-25mg
LDN-192960 (Compd 1) is a potent inhibitor of Haspin and Dual-specificity Tyrosine-regulated Kinase 2 (DYRK2) with IC50 of 10 nM and 48 nM respectively
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Medchemexpress LLC Mutant IDH1 inhibitor | 1429180-08-4 | 99.4% | C25H34N6O3 | 10MG
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Mutant IDH1 inhibitor is a research-grade small molecule that selectively inhibits mutant isocitrate dehydrogenase 1 (IDH1) R132H with sub-100 nM potency. It is supplied as a high-purity solid for biochemical assays and in vitro studies, and is accompanied by documentation for quality control and safe handling.
- High potency against mutant IDH1 R132H (IC50 < 72 nM).
- High purity suitable for research (99.4% by HPLC).
- Molecular formula C25H34N6O3; molecular weight 466.58 g/mol.
- Supplied as a solid, white to light yellow, in small laboratory packaging.
- Recommended storage: powder long-term at -20°C, short-term at 4°C.
- Includes downloadable certificate of analysis and safety data sheet for traceability and safety.
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Cayman Chemical Sodium Phosphate Stock Soluti
A concentrated buffer solution
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Pickering Laboratories Inc Artificial Perspiration, ISO 3160 with added Pyruvic acid, Buffered, Stabilized, each (950 mL/bottle).
This formulation is used to determine corrosion (tarnishing, oxidation and surface penetration) resistance for gold alloy coverings on watch cases and accessories, including bracelets when they are permanently attached to the case. This formulation has an addition of Pyruvic Acid and Phosphate Buffer for added pH stability
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Electron Microscopy Sciences Sodium Bisulfite 1% 500 ML
Used in combined Hematoxylin and Eosin/Methenamine Silver Stain for the fungi in tissue Sections. For bacterial, fungal stains. See references: Lamps, Laura W. et al A Combined Hematoxylin and Eosin/Methenamin Silver Stain for theHistological Diagnosis of Fungi In Tissue Sections., J. of Histotechnology 23:4 p.341 – 345, 2000.
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eMolecules Ambeed / 1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2-(2H-tetrazol-5-yl)-[11-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate / 1mg / 761012559 / A259269 / / 145040-37-5 / MFCD22373650 / 610.671 / C33H34N6O6
Ambeed / 1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2-(2H-tetrazol-5-yl)-[11-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate / 1mg / 761012559 / A259269 / / 145040-37-5 / MFCD22373650 / 610.671 / C33H34N6O6
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Medchemexpress LLC δ-secretase inhibitor 11 | 842964-18-5 | 99.9% | 220.23 g·mol⁻¹ | C10H12N4O2 | 50MG
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δ-Secretase inhibitor 11 is a selective, brain-penetrant small-molecule inhibitor of δ-secretase (asparagine endopeptidase) used for neuroscience and neurodegeneration research. It shows reported in vitro potency and is provided as a characterized research-grade compound with supporting analytical data for assay and in vivo studies.
- Selective δ-secretase inhibition with reported IC50 ≈ 0.7 μM.
- Brain-penetrant and orally active in preclinical models.
- High reported purity suitable for research applications.
- Supplied as a solid with multiple package sizes for experimental flexibility.
- Comprehensive characterization available, including COA, H-NMR, RP-HPLC, and MS.
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Medchemexpress LLC 7-(morpholin-4-yl)-2,1,3-benzoxadiazol-4-amine | 842964-18-5 | MFCD03422529 | 99.9% | 220.23 g/mol | C10H12N4O2 | 10MG
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δ-Secretase inhibitor 11 is a selective, orally active small-molecule inhibitor of δ-secretase used in neurodegeneration research. It is reported to be blood-brain barrier permeable and non-toxic in preclinical models, attenuating pathological cleavage of tau and amyloid precursor protein and improving synaptic function and cognition in relevant transgenic mouse models.
- Selective δ-secretase inhibition with reported IC50 0.7 μM.
- Blood-brain barrier permeable, suitable for in vivo studies.
- Reduces tau and APP cleavage in disease models.
- High reported purity (≈99.9%).
- Available as solid quantities and as 10 mM solution in DMSO.
- Useful for Alzheimer's disease mechanism and therapeutic research.
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Medchemexpress LLC Cathepsin G inhibitor I | 429676-93-7 | MFCD28137715 | ≥99.0% | 620.63 | C36H33N2O6P | 100 MG
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Cathepsin G Inhibitor I is a selective, reversible, competitive, non-peptide inhibitor of cathepsin G used in biochemical and pharmacological research to probe protease activity. It demonstrates potent inhibition and is supplied as a solid with high purity suitable for assay development and mechanistic studies.
- Selective, reversible inhibitor of cathepsin G.
- Potent activity (IC50 53 nM; Ki 63 nM).
- High purity (≥99.0%) for research applications.
- Solid form, convenient for storage and handling.
- Available in milligram-scale quantities for laboratory use.
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Revvity Health Sciences Inc DELFIA Eu-DTPA-DTA Chelate and Europium (Eu) Standard, 2 mg
DELFIA Eu-DTPA-DTA Chelate and Europium (Eu) Standard, 2 mg
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Haztech Systems, Inc Hazcat HW4012-2 Sodium Fusion Test 2 (2ct)
HW4012-2 Sodium Fusion Test 2 (2ct)
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LaMarKa Chemical Company Naphtha Preciptation Grade
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NC1425308 NAPHTHA PRECIPTATION GRADE
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eMolecules D-Galactose-3-sulfate potassium salt | Toronto Research Chemicals |298.300 | C6H11KO9S[K+].OC[C@H]1OC(O)[C@H](O)[C@@H](OS([O-])(=O)=O)[C@H]1O | 0.5mg | 483410172
D-Galactose-3-sulfate potassium salt | Toronto Research Chemicals |298.300 | C6H11KO9S[K+].OC[C@H]1OC(O)[C@H](O)[C@@H](OS([O-])(=O)=O)[C@H]1O | 0.5mg | 483410172
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Medchemexpress LLC Canrenoate potassium | 2181-04-6 | 99.9% | 100 MG
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Canrenoate potassium is a proagent that releases canrenone. It acts as a potent, competitive mineralocorticoid receptor (aldosterone receptor) antagonist. As a diuretic, it is used for hypertension research.
- Proagent that releases canrenone
- Potent, competitive mineralocorticoid receptor antagonist
- Used in hypertension research as a diuretic
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Medchemexpress LLC Ldn-214117 | 1627503-67-6 | 99.5% | 419.52 | 1 ML
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Ldn-214117 | 1627503-67-6 | 99.5% | 419.52 | 1 ML
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