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Filtered Search Results
Medchemexpress LLC Naloxone hydrochloride | 357-08-4 | 99.96% | 363.84 | 100MG
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Naloxone hydrochloride is an opioid receptor antagonist that alleviates opioid-overdose-induced respiratory depression. It is intended for research use only and not for patient administration. The compound may cause pulmonary edema and cardiac arrhythmias. It is soluble in both water and DMSO.
- Acts as an antagonist of the opioid receptor
- Alleviates respiratory depression caused by opioid overdose
- Soluble in water and DMSO for various research applications
- Available in solid, white to off-white appearance
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Medchemexpress LLC CPD-1224 | 2891620-68-9 | C43H47ClN8O7S | 5 MG
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CPD-1224 is an orally effective ALK inhibitor that is a derivative of an ALK inhibitor connected to the cereblon ligand. It targets the EML4-ALK oncogenic fusion protein, degrading both ALK and its mutant forms L1196M/G1202R. This compound has the ability to slow down tumor growth.
- Orally effective ALK inhibitor.
- Targets and degrades the EML4-ALK oncogenic fusion protein.
- Degrades mutant forms L1196M/G1202R of ALK.
- Can slow down tumor growth.
- Significantly enhances kinase binding selectivity and exhibits good degradation selectivity.
- Has 28% oral bioavailability in mice.
- Inhibits tumor growth in mice at a dosage of 10 mg/kg, orally, twice daily for 15 days.
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Medchemexpress LLC Diclofenac methyl es 25mg | 15307-78-5 | 310.18 g/mol | 25 MG
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Diclofenac methyl ester (CAS 15307-78-5) is the methyl ester metabolite of diclofenac provided as a high-purity research reagent for biochemical, toxicological, and analytical studies. The material is supplied in small research packs for use as a reference standard and reagent; users should consult the datasheet and SDS for safety and handling details.
- Provided as a purified reference material suitable for laboratory research.
- Purity ≥98.04% as listed by the supplier.
- Molecular formula C15H13Cl2NO2; molecular weight 310.18 g/mol.
- 25 mg pack size suitable for method development and analytical work.
- Intended for research use only; not for human or veterinary use.
- Consult the product datasheet and SDS for storage and handling instructions.
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Cambridge Isotope Laboratories Nornicotine (unlabeled) 100 ug/mL in MTBE 1 2 mL
Nornicotine (unlabeled) 100 ug/mL in MTBE 1 2 mL
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Emergency Medical Products Inc LIDOCAINE AMPULE 2ML 50/PK
This item has a minimum qty of 3 per supplier requirements.
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Medchemexpress LLC METOCLOPRAMIDE | 500MG
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METOCLOPRAMIDE | 500MG
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Medchemexpress LLC Loratadine (Standard) | 79794-75-5 | MFCD00672869 | 99.9% | 382.88 | 25 MG
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Loratadine (Standard) is an analytical standard intended for research and analytical applications. It acts as a selective inverse peripheral histamine H1-receptor agonist and has anti-dengue-virus (DENV) activity. This compound can also inhibit the immunologic release of inflammatory mediators.
- Selective inverse peripheral histamine H1-receptor agonist
- Anti-dengue-virus (DENV) activity
- Inhibits immunologic release of inflammatory mediators
- Analytical standard for research and analytical applications
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Sigma Aldrich Fine Chemicals Biosciences Bufexamac impurity B European Pharmacopoeia (EP) Reference Standard | 29056-06-2 |
Bufexamac impurity B European Pharmacopoeia (EP) Reference Standard | Mol Wt: 222.28 | 29056-06-2 |
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000381650 ONX-0914 50MG
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Medchemexpress LLC Mevastatin | 73573-88-3 | 390.51 | 1 ML
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Mevastatin (Compactin) is the first HMG-CoA reductase inhibitor belonging to the statins class. It acts as a lipid-lowering agent, induces apoptosis, and arrests cancer cells in the G0/G1 phase. It also increases endothelial nitric oxide synthase (eNOS) mRNA and protein levels. This compound exhibits antitumor activity and shows potential for treating cardiovascular diseases.
- HMG-CoA reductase inhibitor
- Lipid-lowering agent
- Induces apoptosis and arrests cancer cells in G0/G1 phase
- Increases endothelial nitric oxide synthase (eNOS) mRNA and protein levels
- Exhibits antitumor activity
- Potential for cardiovascular diseases treatment
- Targets metabolic enzyme/protease, autophagy, apoptosis, and anti-infection pathways
- Research areas include infection, cardiovascular disease, neurological disease, metabolic disease, and cancer
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Sigma Aldrich Fine Chemicals Biosciences Penbutolol sulfate European Pharmacopoeia (EP) Reference Standard | 38363-32-5 |
Penbutolol sulfate European Pharmacopoeia (EP) Reference Standard | Mol Wt: 680.94 | 38363-32-5 |
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Medchemexpress LLC Febantel | 58306-30-2 | 99.9% | 446.48 | 10 G
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Febantel is an oral dewormer utilized for treating gastrointestinal nematodes in sheep, as well as roundworm and tapeworm infections in poultry and livestock. It also hinders the embryonic development of mouse hairworms and whipworm eggs.
- Treats gastrointestinal nematodes in sheep
- Treats roundworm and tapeworm infections in poultry and livestock
- Inhibits embryonic development of mouse hairworms
- Inhibits embryonic development of whipworm eggs
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Medchemexpress LLC Doxazosin mesylate | 77883-43-3 | 98.5% | C24H29N5O8S | 1 ML
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Doxazosin mesylate is a quinazoline-derivative that selectively antagonizes postsynaptic α1-adrenergic receptors. It is the mesylate salt form of doxazosin, a long-lasting inhibitor of α1-adrenoceptors widely used to treat benign prostatic hyperplasia and lower urinary tract symptoms. It may also have a direct inhibitory effect on cholesterol synthesis, potentially leading to upregulation of the LDL receptor and a reduction in LDL cholesterol.
- Selectively antagonizes postsynaptic α1-adrenergic receptors
- Long-lasting inhibitor of α1-adrenoceptors
- Used to treat benign prostatic hyperplasia and lower urinary tract symptoms
- May have a direct inhibitory effect on cholesterol synthesis
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Medchemexpress LLC (rel)-Tivantinib | 905853-99-8 | 96.5% | C23H19N3O2 | 1 ML
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(rel)-Tivantinib is a potent and highly selective inhibitor of the receptor tyrosine kinase c-MET. It also targets GSK3α and GSK3β, which are significant in the cellular mechanism of non-small cell lung cancer (NSCLC). This product is intended for research use only.
- Potent and highly selective inhibitor of c-MET
- Targets GSK3α and GSK3β
- Important in the cellular mechanism of non-small cell lung cancer (NSCLC)
- For research use only
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Sigma Aldrich Fine Chemicals Biosciences Glipizide impurity A European Pharmacopoeia (EP) Reference Standard | 33288-71-0 |
Glipizide impurity A European Pharmacopoeia (EP) Reference Standard | Mol Wt: 320.37 | 33288-71-0 |
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