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Filtered Search Results
LaMarKa Chemical Company Aminoantipyrine (AAP) Solution, 500ml
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Aminoantipyrine (AAP) Solution, 4-Aminoantipyrine, 83-07-8, WT%: < 3%, 500ml
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LaMarKa Chemical Company Hydrochloric Acid 0.1N Methyl Red/THAM Endpoint, 4l
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Hydrochloric Acid 0.1N Methyl Red/THAM Endpoint, 4l Plastic Jug
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Medchemexpress LLC Chromium(III) potassium sulfate dodecahydrate | 7788-99-0 | MFCD00149917 | ≥98.0% | 499.40 | KCr(SO4)2·12H2O | 500 G
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Chromium(III) potassium sulfate dodecahydrate (≥98%) is a research-grade inorganic reagent commonly used as a fixative in microscopic analysis and in analytical or preparative laboratory applications. It is supplied as a pale purple crystalline solid with formula KCr(SO4)2·12H2O and molecular weight 499.40.
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LaMarKa Chemical Company Mixed Acid Solution contains Sulfuric Acid & Phosphoric Acid, 4l
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Mixed Acid Solution contains Sulfuric Acid & Phosphoric Acid, 4l Plastic Jug
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Aqua Solutions Litmus 0.5% w/v Solution (500ML)
Litmus 0.5% w/v Solution (500ML)
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Medchemexpress LLC Cathepsin G inhibitor I | 429676-93-7 | MFCD28137715 | >=99.0% | 620.63 | C36H33N2O6P | 25 MG
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Cathepsin G Inhibitor I is a selective, reversible, competitive, non-peptide inhibitor of cathepsin G with nanomolar potency (IC50 = 53 nM; Ki = 63 nM). It is provided in both solid and DMSO solution formats for use in biochemical and cell-based assays to study serine protease inhibition.
- Selective inhibition of cathepsin G (IC50 53 nM; Ki 63 nM).
- Reversible, competitive, non-peptide mechanism suitable for biochemical assays.
- Available in multiple solid quantities and solution formats for assay flexibility.
- High purity (≥99.0%) for reproducible results.
- Molecular weight 620.63 and molecular formula C36H33N2O6P.
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Medchemexpress LLC Kv2 channel inhibitor-1 | 689297-68-5 | MFCD32631937 | 98.7% | 396.89 | C20H17ClN4OS | 10 MG
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KV2 channel inhibitor-1 is a selective small-molecule inhibitor of KV2 family potassium channels, with potent activity against KV2.1 (IC50 0.2 μM) and KV2.2 (IC50 0.41 μM). It is supplied as a solid research compound for in vitro electrophysiology and pharmacological profiling, with reported selectivity data versus other voltage-gated ion channels.
- Selective inhibition of KV2.1 and KV2.2 (IC50 0.2 μM and 0.41 μM).
- High purity suitable for research use.
- Provided as a white to off-white solid for assay work.
- Includes selectivity data against KV, CaV, and NaV channels.
- Available in small milligram quantities for in vitro studies.
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Medchemexpress LLC Tie2 kinase inhibitor 1 | 948557-43-5 | 99.8% | 439.53 | C26H21N3O2S | 1 ML
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Tie2 kinase inhibitor 1 is a potent, selective small-molecule inhibitor of the Tie2 receptor tyrosine kinase with reported anti-cancer activity. It inhibits Tie2 with an IC50 of 250 nM and is supplied for research use.
- Potent Tie2 inhibition with IC50 of 250 nM.
- High purity suitable for research applications (reported 99.8%).
- Characterized small molecule: formula C26H21N3O2S, molecular weight 439.53.
- Physical form light yellow to yellow solid.
- Available as concentrated solution for assay convenience.
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Medchemexpress LLC DTPA-tetra (t-Bu ester) | 174267-71-1 | 99.0% | 617.77 g·mol⁻¹ | C30H55N3O10 | 10 MG
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DTPA-tetra (t-Bu ester) is the tetra-tert-butyl ester derivative of diethylenetriaminepentaacetic acid (DTPA). It serves as a bifunctional chelator for use in bioconjugation and radiolabeling workflows, enabling conjugation of peptides and radionuclides for labeling and tumor pre-targeting research applications.
- Bifunctional chelator for peptide and radionuclide conjugation.
- Tetra-tert-butyl ester derivative that facilitates protection and conjugation chemistry.
- High purity (≈99.0%) suitable for research applications.
- Molecular weight 617.77 g·mol⁻¹ and molecular formula C30H55N3O10.
- Supplied as small quantities for labeling and method development workflows.
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Apexbio Technology LLC DEET 134-62-3 1g
DEET (134-62-3) is a small-molecule antagonist targeting insect odorant receptors It is designed to disrupt molecular interactions within chemosensory pathways thereby inhibiting insect attraction and biting behavior DEET exerts its biological activity primarily through interference with insect odorant receptors In in vitro and behavioral assays DEET demonstrates inhibitory activity with variable IC50 values reported for receptor modulation and insect behavioral responses Based on these pharmacological properties DEET holds research potential in evaluating insect chemoreception and vector-host interactions relevant to the transmission of pathogens such as Zika virus malaria parasites West Nile virus Lyme disease-causing bacteria and Rocky Mountain spotted fever agents
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Medchemexpress LLC Mutant EGFR inhibitor | 1421373-62-7 | 99.4% | 520.03 | 50 MG
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Mutant EGFR inhibitor (Example 25) is a potent mutant EGFR inhibitor. It inhibits FGFRWT with an IC50 of 0.41 nM. This inhibitor also targets EGFRL858R, EGFRExon 19 deletion, and EGFRT790M. It is intended for the study of diseases mediated by EGFR, especially cancers, and is for research use only, not for sale to patients.
- Potent mutant EGFR inhibitor
- Inhibits FGFRWT with an IC50 of 0.41 nM
- Targets EGFRL858R, EGFRExon 19 deletion, and EGFRT790M
- Used for the study of diseases mediated by EGFR, particularly cancers
- For research use only
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Medchemexpress LLC Deschloroetizolam | 40054-73-7 | 99.8% | 308.41 | 100 MG
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Deschloroetizolam is a designer Benzodiazepine, a psychoactive substance with physical and cognitive effects. It is intended for research use only, not for sale to patients. This solid, white to off-white compound has a molecular weight of 308.41. It exhibits high solubility in DMSO, reaching 125 mg/mL (405.30 mM).
- Intended for research use only
- Psychoactive substance with physical and cognitive effects
- Appears as a white to off-white solid
- Highly soluble in DMSO (125 mg/mL)
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Medchemexpress LLC Mutant IDH1 inhibitor | 1429180-08-4 | 99.1% | 466.58 | 10 MM 1 ML
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Mutant IDH1 inhibitor is a potent mutant IDH1 R132H inhibitor with an IC50 of < 72 nM. It is used for the treatment of diseases or disorders associated with such mutant IDH proteins, including cell-proliferation disorders, such as cancer.
- Potent mutant IDH1 R132H inhibitor
- IC50 of < 72 nM
- Treats diseases associated with mutant IDH proteins
- Applicable for cell-proliferation disorders including cancer
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LaMarKa Chemical Company Phenolphthalein Indicator 0.5% W/V (5 gpl) in Ethanol, 0.1l
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Phenolphthalein Indicator 0.5% W/V (5 gpl) in Ethanol, 0.1l Plastic Bottle
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LaMarKa Chemical Company Reagent #1 (Degassed w/Helium) Hydrochloric 20%/Phosphoric 20%, 4l
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Reagent #1 (Degassed w/Helium) Hydrochloric 20%/Phosphoric 20%, 4l Plastic Jug
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