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Filtered Search Results
Medchemexpress LLC HY-13588 100mg Medchemexpress, Cefsulodin (sodium) CAS:52152-93-9 Purity:>98%
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Medchemexpress, HY-13588 100mg Cefsulodin (sodium) CAS:52152-93-9 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-13582 100mg Medchemexpress, Carbendazim CAS:10605-21-7 Purity:>98%
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Medchemexpress, HY-13582 100mg Carbendazim CAS:10605-21-7 Carbendazim is a potent and orally active broad-spectrum benzimidazole fungicide and can be acts as a pesticide for fungal diseases research, such as Seproria, Fusarium and Sclerotina. Carbendazim is a benzimidazole (HY-Y1825) derivative with antitumor activity and used for cancer research, especially advanced solid tumors and lymphoma. 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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Apexbio Technology LLC Vancomycin hydrochloride, 1g Cas# 1404-93-9
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Vancomycin hydrochloride is a hydrochloride of vancomycin that is a narrow-spectrum glycopeptide antibacterial agent. 1404-93-9. MFCD03613611 Vancomycin hydrochloride is a hydrochloride of vancomycin that is a narrow-spectrum glycopeptide antibacterial agent. There are other sizes available. Please inqury us for quote.
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Medchemexpress LLC HDAC-IN-4 | >98.0% | 100 MG
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HDAC-IN-4 is a selective inhibitor of Histone Deacetylase (HDAC) 6 and HDAC10. It demonstrates potent inhibitory activity against these enzymes, with pIC50 values of 7.2 for HDAC6 and 6.8 for HDAC10 in BRET assays.
- Selective HDAC6 and HDAC10 inhibitor
- Antitumoral activity
- pIC50 of 7.2 for HDAC6 in BRET assay
- pIC50 of 6.8 for HDAC10 in BRET assay
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Medchemexpress LLC HY-13439 5mg Medchemexpress, SR144528 CAS:192703-06-3 Purity:>98%
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Medchemexpress, HY-13439 5mg SR144528 CAS:192703-06-3 SR144528 is a potent and selective CB2 receptor antagonist with a Ki of 0.6 nM. 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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Cambridge Isotope Laboratories CORTISONE (2,3,4-13C3, 98%) CP 97% 100 U, 1 ML
CORTISONE (2,3,4-13C3, 98%) CP 97% 100 U, 1 ML
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AdipoGen Lactacystin, 133343-34-7, MFCD01076525, 200 ug
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MF: C15H24N2O7S, MW: 376.4, ≥98%, Appearance: White to off-white solid. Induces neuritogenesis, Apoptosis inducer, Anticancer compound, and Induces differentiation and inhibits cell cycle progression in several tumor cell lines.
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Sigma Aldrich Fine Chemicals Biosciences Chlortetracycline hydrochloride >=91.0% dry basis (HPLC) | 64-72-2 | MFCD00082440 | 25G
Chlortetracycline hydrochloride >=91.0% dry basis (HPLC) | Purity: >=91.0% dry basis (HPLC) | Mol Wt: 515.34 | 64-72-2 | MFCD00082440 | 25G
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Medchemexpress LLC 3-[(4-chlorophenyl)methoxy]-N-[(1S)-1-phenylethyl]thiophene-2-carboxamide | 1203680-76-5 | MFCD18086887 | >98.0% | 371.88 g/mol | C20H18ClNO2S | 10 MG
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AS1949490 (3-[(4-chlorophenyl)methoxy]-N-[(1S)-1-phenylethyl]thiophene-2-carboxamide) is a potent, orally active, and selective inhibitor of SHIP2 phosphatase used for research into insulin signaling and metabolic disease. It increases Akt phosphorylation, glucose consumption, and glucose uptake in cellular models. Intended for research use only, it has a molecular weight of 371.88 g/mol and CAS 1203680-76-5.
- Selective SHIP2 inhibitor with nanomolar activity for mouse and human SHIP2.
- Promotes Akt phosphorylation and increases glucose uptake in cells.
- Suitable for metabolic and diabetes research applications.
- Molecular formula C20H18ClNO2S and molecular weight 371.88 g/mol.
- Typical supplier-reported purity ≥98% (HPLC).
- Powder stable at -20 °C; in solution stable at -80 °C (6 months) or -20 °C (1 month).
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Chem-Impex International, Inc. Teicoplanin | 61036-64-4 | MFCD05664625 | 100MG
Teicoplanin, 61036-64-4, MFCD05664625, 100MG
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Medchemexpress LLC HY-A0096 100mg , Iloprost Ciloprost;ZK 36374 CAS:78919-13-8 Purity:98%
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Medchemexpress, HY-A0096 100mg Iloprost Ciloprost;ZK 36374 CAS:78919-13-8 Formula:C22H32O4 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 Sodium copper chlorophyllin B | 28302-36-5 | 500 MG
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Sodium copper chlorophyllin B is a compound that demonstrates antiviral activities against Influenza virus and HIV, with IC50s ranging from 50 to 100 μM for both. It is intended for research use only and exhibits inhibition of influenza virus adsorption at 200 μM and HIV adsorption at 2.5 mM.
- Antiviral activity against influenza virus and HIV.
- IC50s of 50 to 100 μM for both influenza virus and HIV.
- Inhibits influenza virus adsorption at 200 μM.
- Inhibits HIV adsorption at 2.5 mM.
- Intended for research use only.
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Medchemexpress LLC Hygromycin A | 6379-56-2 | 511.48 | 1 MG
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Hygromycin A is a Borrelia burgdorferi-selective antibiotic. It is a spirochete-specific antibacterial that is conducive to gut health and can be used for Lyme disease research.
- Spirochete-specific antibacterial
- Contributes to gut health
- Used for Lyme disease research
- Selectively kills Borrelia burgdorferi in vivo
- Positively impacts gut microbiota composition, leading to eubiosis
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Medchemexpress LLC Erythromycin estolate | 3521-62-8 | 100 MG
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Erythromycin estolate is a macrolide antibiotic derived from Erythromycin, utilized for treating a broad spectrum of bacterial infections. It has been noted to cause liver injury, often presenting as cholestatic hepatitis, with its toxicity linked to inhibiting bile acid transport. This compound also exhibits antiviral properties by inactivating viral particles and destroying their membrane integrity.
- Used as a macrolide antibiotic.
- Effective against a wide variety of bacterial infections.
- Causes liver injury, predominantly cholestatic hepatitis.
- Toxicity is associated with inhibiting bile acid transport.
- Inactivates viral particles by destroying viral membrane integrity.
- Inhibits various flaviviruses, including Zika, dengue, and yellow fever viruses.
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Medchemexpress LLC Spiramycin I | 24916-50-5 | 10 MG
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Spiramycin I is a macrolide antibiotic and antiparasitic that inhibits protein synthesis by binding to the 50S ribosomal subunit in bacteria. It is effective against various Gram-positive bacteria and protozoal infections, including Toxoplasma gondii. It can also prevent the placental transmission of toxoplasmosis.
- Antibiotic and antiparasitic agent
- Inhibits Gram-positive bacteria
- Effective against protozoal infections
- Prevents placental transmission of toxoplasmosis
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