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Filtered Search Results
Medchemexpress LLC Cefazolin | 25953-19-9 | 99.7% | 100 MG
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Cefazolin (Cephazolin) is a first-generation cephalosporin antibiotic that can be used in research for various bacterial infections. It also exhibits anti-inflammatory effects and can mitigate post-operative cognitive dysfunction (POCD).
- Antibiotic properties: First-generation cephalosporin antibiotic effective against various bacterial infections.
- Anti-inflammatory effect: Can attenuate post-operative cognitive dysfunction (POCD).
- High purity of 99.73%.
- Research use only.
- Versatile forms: Available as a solid and in solution.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Piroctone olamine | 68890-66-4 | 99.7% | 500 MG
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Piroctone olamine is a pyridine derivative with a fungicidal effect. It acts as a hydroxypyridone anti-mycotic agent by penetrating cell membranes and forming complexes with iron ions, thereby inhibiting energy metabolism in mitochondria.
- Fungicidal effect
- Demonstrates low minimum inhibitory concentrations for Candida strains
- Reduces fungal growth in intra-abdominal candidiasis in experimental models
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Medchemexpress LLC Suramin (sodium salt) | 129-46-4 | MFCD00003780 | 100.0% | 50 MG
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Suramin sodium salt is a reversible and competitive inhibitor of protein-tyrosine phosphatases (PTPases). It also potently inhibits sirtuins (SirT1, SirT2, SirT5), acts as a competitive inhibitor of reverse transcriptase (DNA topoisomerase II), and functions as a potent SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibitor. Additionally, it efficiently inhibits IP5K and acts as an antiparasitic, anti-neoplastic, and anti-angiogenic agent.
- Reversible and competitive PTPases inhibitor
- Potent inhibitor of sirtuins (SirT1, SirT2, SirT5)
- Competitive inhibitor of reverse transcriptase (DNA topoisomerase II)
- Potent SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibitor
- Efficiently inhibits IP5K
- Acts as an antiparasitic, anti-neoplastic, and anti-angiogenic agent
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eMolecules 2308-18-1 | Acetoacetic Acid Isoamyl Ester | Toronto Research Chemicals | MFCD00059355 | 172.224 | C9H16O3CC(C)CCOC(=O)CC(C)=O | 500mg | 601588878
Acetoacetic Acid Isoamyl Ester | Toronto Research Chemicals | 2308-18-1 | MFCD00059355 | 172.224 | C9H16O3CC(C)CCOC(=O)CC(C)=O | 500mg | 601588878
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Medchemexpress LLC HY-10492 10mg Medchemexpress, Dinaciclib CAS:779353-01-4 Purity:>98%
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Medchemexpress, HY-10492 10mg Dinaciclib CAS:779353-01-4 Dinaciclib (SCH 727965) is a potent inhibitor of CDK, with IC50s of 1 nM, 1 nM, 3 nM, and 4 nM for CDK2, CDK5, CDK1, and CDK9, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-15695 500mg Medchemexpress, Puromycin aminonucleoside CAS:58-60-6 Purity:>98%
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Medchemexpress, HY-15695 500mg Puromycin aminonucleoside CAS:58-60-6 Puromycin aminonucleoside (NSC 3056) is the aminonucleoside portion of the antibiotic puromycin, and used in nephrosis animal models. Puromycin aminonucleoside induces apoptosis[2]. Puromycin aminonucleoside is a reversible inhibitor of dipeptidyl peptidase II and cytosol alanyl aminopeptidase[3]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-13018 10mg Medchemexpress, MRT67307 CAS:1190378-57-4 Purity:>98%
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Medchemexpress, HY-13018 10mg MRT67307 CAS:1190378-57-4 MRT67307 is a dual inhibitor of the IKKε and TBK-1 with IC50s of 160 and 19 nM, respectively. MRT67307 also inhibits ULK1 and ULK2 with IC50s of 45 and 38 nM, respectively. MRT67307 also blocks autophagy in cells[2]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC SAR405 | 1523406-39-4 | MFCD28411361 | >98.0% | 443.9 | C19H21ClF3N5O2 | 2MG
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SAR405 is a research-grade small-molecule inhibitor of the class III phosphatidylinositol 3-kinase (Vps34/PIK3C3). It potently inhibits Vps34 activity (reported IC50 = 1.2 nM; Kd = 1.5 nM) and is used in cellular and biochemical studies to block autophagosome formation and alter vesicle trafficking. Supplied as a high-purity solid suitable for laboratory research.
- Potent Vps34 inhibitor (IC50 = 1.2 nM).
- Blocks autophagosome formation and inhibits autophagy.
- Useful for cellular and biochemical studies of vesicle trafficking.
- Supplied as a high-purity solid or powder for research use.
- Available in small, research-scale quantities suitable for assay development.
- Characterized in peer-reviewed publications for target engagement.
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Medchemexpress LLC HY-B0795 5mg Medchemexpress, MHY1485 CAS:326914-06-1 Purity:>98%
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Medchemexpress, HY-B0795 5mg MHY1485 CAS:326914-06-1 MHY1485 is a potent cell-permeable mTOR activator that targets the ATP domain of mTOR. MHY1485 inhibits autophagy by suppression of fusion between autophagosomes and lysosomes Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 53123-88-9 | Rapamycin | Adipogen914.187 | C51H79NO13 | 98.000 | CO[C@@H]1C[C@H](C[C@@H](C)[C@@H]2CC(=O)C(C)\C=C(C)\[C@@H](O)[C@@H](OC)C(=O)[C@H](C)C[C@H](C)\C=C\C=C\C=C(C)\[C@H](C[C@H]3CC[C@@H](C)[C@](O)(O3)C(=O)C(=O)N3CCCC[C@H]3C(=O)O2)OC)CC[C@H]1O | 1mg | 632804614
Rapamycin | Adipogen | 53123-88-9914.187 | C51H79NO13 | 98.000 | CO[C@@H]1C[C@H](C[C@@H](C)[C@@H]2CC(=O)C(C)\C=C(C)\[C@@H](O)[C@@H](OC)C(=O)[C@H](C)C[C@H](C)\C=C\C=C\C=C(C)\[C@H](C[C@H]3CC[C@@H](C)[C@](O)(O3)C(=O)C(=O)N3CCCC[C@H]3C(=O)O2)OC)CC[C@H]1O | 1mg | 632804614
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TOKU-E Clarithromycin ReadyMade™ Solution | CAS 81103-11-9 | 1 mg/ml in water | sterile-filtered | 10 x 1 ml
Clarithromycin ReadyMade™ Solution | CAS 81103-11-9 | 1 mg/ml in water | sterile-filtered | 10 x 1 ml
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TOKU-E Trimethoprim ReadyMade™ Solution | 738-70-5 | 25 mg/ML in DMSO | filter-sterile | 10 x 1 ML
Trimethoprim ReadyMade™ Solution | 738-70-5 | 25 mg/ML in DMSO | filter-sterile | 10 x 1 ML
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TOKU-E Daptomycin ReadyMade™ Solution | CAS 103060-53-3 | 1 mg/ML in 10% beta-cyclodextrin saline solution | sterile-filtered | 10 x 0.5 ML
Daptomycin ReadyMade™ Solution | CAS 103060-53-3 | 1 mg/ML in 10% beta-cyclodextrin saline solution | sterile-filtered | 10 x 0.5 ML
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TOKU-E Co-trimoxazole ReadyMade™ Solution | CAS 8-64-90-2 | 100 mg/ML in DMSO | sterile-filtered | 10 x 1 ML
Co-trimoxazole ReadyMade™ Solution | CAS 8-64-90-2 | 100 mg/ML in DMSO | sterile-filtered | 10 x 1 ML
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Research Products International Corp RPI Anisomycin from streptomyces griseolus [2-[(4-Methoxyphenyl)methyl]-3, 4-pyrrolidinediol-3-acetate], 500 Milligrams
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Anisomycin is an antibiotic derived from Streptomyces griseolus. It inhibits protein synthesis in eukaryotic cells by blocking the peptidyl transferase activity of the 60S ribosomal subunit. This interference disrupts the elongation phase of protein synthesis, leading to the inhibition of new protein formation.
Anisomycin is widely used as a tool in cell biology and biochemistry to study cellular responses to stress, apoptosis, and various signaling pathways. Its ability to selectively inhibit protein synthesis allows researchers to investigate the role of specific proteins in cellular processes. Anisomycin induces cellular stress and activates various stress response pathways, making it valuable in studies focused on understanding how cells respond to environmental challenges.
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