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Filtered Search Results
Medchemexpress LLC Teglicar | 250694-07-6 | 98.0% | 399.61 | 5 MG
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Teglicar is a selective and reversible orally active liver isoform of carnitine palmitoyl-transferase 1 (L-CPT1) inhibitor with an IC50 value of 0.68 μM and a Ki value of 0.36 μM. Teglicar has a potential antihyperglycemic property. It can be used for the research of diabetes and neurodegenerative disease including Huntington's disease (HD).
- Selective and reversible orally active liver isoform of carnitine palmitoyl-transferase 1 (L-CPT1) inhibitor.
- Has an IC50 value of 0.68 μM and a Ki value of 0.36 μM for L-CPT1.
- Possesses potential antihyperglycemic properties.
- Suitable for research on diabetes and neurodegenerative diseases, such as Huntington's disease (HD).
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MEDCHEMEXPRESS LLC FICZ 5MG
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501872658 FICZ 5MG
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eMolecules 331963-29-2 | Medchem Express | I2906 | 100mg | 446271477 | HY-76293 | MFCD01128075 | 443.588 | C25H37N3O4
AbaChemScene | Ethyl (E)-3-morpholinoacrylate | 100mg | 410753097 | CS-0047053 | 81239-01-2 | MFCD28252204 | 185.223 | C9H15NO3
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MEDCHEMEXPRESS LLC S-JQ-35 5MG
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501872544 S-JQ-35 5MG
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MEDCHEMEXPRESS LLC AKOS B018304 5MG
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501872547 AKOS B018304 5MG
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MEDCHEMEXPRESS LLC PROPINEB 100MG
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501872561 PROPINEB 100MG
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AdipoGen Puromycin Dihydrochloride, 58-58-2, MFCD00012691, 1 g
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MF: C22H29N7O5 . 2HCl, MW: 544.437, ≥98%, Appearance: White to off-white powder. Aminonucleoside antibiotic. Protein synthesis inhibitor. Disrupts peptide transfer on ribosomes (acting as an acyl-tRNA analog) causing premature chain termination during translation. Translational inhibitor in prokaryotic and eukaryotic cells in both in vitro and in vivo systems. Inhibits the transport of proteins into the mitochondria in vitro. Reversible inhibitor of dipeptidyl-peptidase II (serine peptidase) and cytosol alanyl aminopeptidase (metallopeptidase). Apoptosis inducer. Inhibits the growth of Gram-positive bacteria, various animal and insect cells. Fungi and Gram-negative bacteria are resistant due to the low permeability to the antibiotic. Antineoplastic agent.
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Alkali Scientific Rapamycin, 1 Mg
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Rapamycin (1mg) is a laboratory reagent primarily used as a cell growth inhibitor in biological research. It works by binding to the mTOR (mechanistic target of rapamycin) protein, inhibiting its activity and thus preventing cell division and growth. This makes it an essential tool in cancer research, immunology, and the study of cell signaling pathways. Rapamycin has also been shown to have immunosuppressive properties, making it useful in transplant medicine to prevent organ rejection. In research, it is used to explore pathways related to aging, metabolism, and diseases associated with uncontrolled cell growth, such as cancer.
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Medchemexpress LLC AZITHROMYCIN HYDRAT | 100MG
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AZITHROMYCIN HYDRAT | 100MG
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Medchemexpress LLC Loratadine-d5 | 1398065-63-8 | 99.96% | 387.91 | 5 MG
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Loratadine-d5 is the deuterium labeled Loratadine. Loratadine (SCH-29851) is a selective inverse peripheral histamine H1-receptor agonist with an IC50 of >32 μM. It has anti-dengue-virus (DENV) activity and can inhibit immunologic release of inflammatory mediators. It can be used as a tracer or an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS. Deuteration has gained attention due to its potential to affect the pharmacokinetic and metabolic profiles of drugs.
- Selective inverse peripheral histamine H1-receptor agonist.
- Has anti-dengue-virus (DENV) activity.
- Can inhibit immunologic release of inflammatory mediators.
- Can be used as a tracer or an internal standard for quantitative analysis.
- Deuteration can affect the pharmacokinetic and metabolic profiles of drugs.
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Medchemexpress LLC Tipiracil hydrochloride | 183204-72-0 | 99.9% | C9H12Cl2N4O2 | 5 MG
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Tipiracil hydrochloride is a thymidine phosphorylase inhibitor (TPI) primarily utilized in cancer research. It demonstrates antiangiogenic effects and effectively inhibits the proliferation of endothelial cells.
- Potent inhibitor of thymidine phosphorylase
- Used for cancer research
- Exhibits antiangiogenic effects
- Inhibits proliferation of endothelial cells
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MEDCHEMEXPRESS LLC PUROMYCIN DIHYDROCHLORIDE 10
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501874583 PUROMYCIN DIHYDROCHLORIDE 10
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Alkali Scientific Anisomycin from streptomyces griseolus [2 [(4 Methoxyphenyl)methyl] 3, 4 pyrrolidinediol 3 acetate], 500 Mg
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Anisomycin is a well established protein synthesis inhibitor used extensively in biochemical and cellular research. It acts by binding to the 60S ribosomal subunit and preventing peptide bond formation, thereby blocking translation. In addition to its inhibitory effects, anisomycin activates stress related pathways such as MAPK signaling, making it a valuable tool for studying cellular responses to stress and apoptosis. Researchers use it in gene expression studies, cancer research, and neuroscience applications. Supplied in a 500 mg quantity, it is suitable for large scale experiments and repeated use in laboratory research protocols.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000669917 PENICILLIN-STREPTOMY 10ML
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Medchemexpress LLC Oss 128167 | 887686-02-4 | 98.6% | 366.32 | C19H14N2O6 | 25 MG
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OSS_128167 is a research-use small molecule that selectively inhibits sirtuin 6 (SIRT6). It has been characterized in cellular and animal studies and shows activity on histone acetylation, metabolic regulation, antiviral effects against hepatitis B virus, and chemosensitization in cancer models. Supplied as a high-purity solid.
- Selective SIRT6 inhibition (IC50 = 89 μM).
- Lower activity against SIRT1 and SIRT2 (IC50s = 1578 μM and 751 μM).
- Demonstrated anti-HBV activity in vitro and in vivo.
- Increases H3K9 acetylation and GLUT-1 expression in cells.
- Induces chemosensitization in multiple myeloma cell lines.
- High reported purity and supplied as a white to light yellow solid.
- For research use only; not for human or clinical use.
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