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Filtered Search Results
MEDCHEMEXPRESS LLC DECOQUINATE 100MG
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501874311 DECOQUINATE 100MG
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MEDCHEMEXPRESS LLC LASALOCID SODIUM 10MG
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501874337 LASALOCID SODIUM 10MG
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Alkali Scientific Amphotericin B, 5 G
Amphotericin B is a polyene antifungal agent widely used in laboratory research to prevent fungal contamination in cell culture and microbiological studies. It interacts with ergosterol in fungal membranes, creating pores that disrupt membrane integrity and result in cell death. This makes it highly effective against a broad range of fungi. In laboratory workflows, it is commonly used to maintain sterile culture environments and protect experimental samples from fungal overgrowth. Amphotericin B is also employed in antifungal susceptibility testing and research focused on fungal biology, providing consistent and reliable antifungal activity.
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Medchemexpress LLC HY-10004 10mg Medchemexpress, Faropenem daloxate CAS:141702-36-5 Purity:>98%
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Medchemexpress, HY-10004 10mg Faropenem daloxate CAS:141702-36-5 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-12203 100mg , PFK-158 CAS:1462249-75-7 Purity:98%
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Medchemexpress, HY-12203 100mg PFK-158 CAS:1462249-75-7 Formula:C18H11F3N2O 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 Levofloxacin 100986-85-4 5g
Levofloxacin (CAS 100986-85-4) is a small-molecule inhibitor targeting bacterial DNA gyrase (topoisomerase II) It modulates DNA supercoiling thereby regulating DNA replication and transcription in bacteria Levofloxacin exerts its biological activity primarily through stabilization of the DNA enzyme cleavage intermediate interfering with DNA replication and causing bacterial cell death In in vitro studies Levofloxacin demonstrates antibacterial inhibitory activity with IC50 values typically ranging from approximately 0 5 g/mL to 4 g/mL depending on bacterial species and experimental conditions Based on these pharmacological properties Levofloxacin holds research potential in studies involving bacterial susceptibility profiling and the development of antibiotic resistance
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Medchemexpress LLC HY-70037A 10mg Medchemexpress, Cinacalcet (hydrochloride) CAS:364782-34-3 Purity:>98%
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Medchemexpress, HY-70037A 10mg Cinacalcet (hydrochloride) CAS:364782-34-3 Cinacalcet hydrochloride (AMG-073 hydrochloride) is an orally active, allosteric agonist of Ca receptor (CaR), used for cardiovascular disease treatment. 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 Solithromycin | 760981-83-7 | 99.85% | 845.01 | 100 MG
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Solithromycin is an orally bioavailable, effective antimicrobial agent. It inhibits cell viability, protein synthesis, and growth rate against various bacteria, including *Streptococcus pneumonia*, *Staphylococcus aureus*, and *Haemophilus influenzae*. This macrolide binds to the large 50S subunit of the ribosome, thereby inhibiting protein biosynthesis.
- Orally bioavailable and effective antimicrobial agent
- Inhibits protein synthesis by binding to the large 50S ribosomal subunit
- Macrolide
- Inhibits TNFa and CXCL8 release
- Reduces MMP9 activity
- Suppresses lipopolysaccharide-induced TNFa release and PMA-induced MMP9 activity
- Does not affect cell viability in monocytic U937 and PBMC cells
- Inhibits inflammatory cells accumulation and pro-MMP9 production in cigarette smoke-exposed mice
- Inhibits cigarette smoke-induced neutrophilia and pro-MMP9 production
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![Medchemexpress LLC 2-[(1R)-1-[2-[4-methoxy-3-(2-morpholin-4-ylethoxy)phenyl]-5-methyl-1,3-thiazol-4-yl]ethyl]sulfanyl | 2107280-55-5 | MFCD34469884 | 99.5% | C23H30N6O3S2 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000258317.png-250.jpg)
Medchemexpress LLC 2-[(1R)-1-[2-[4-methoxy-3-(2-morpholin-4-ylethoxy)phenyl]-5-methyl-1,3-thiazol-4-yl]ethyl]sulfanyl | 2107280-55-5 | MFCD34469884 | 99.5% | C23H30N6O3S2 | 10MG
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DI-87 is an orally active, selective deoxycytidine kinase (dCK) inhibitor developed for anticancer research. It exhibits potent biochemical activity in the low-nanomolar range and has demonstrated antitumor effects in preclinical models, where it is used to enhance the efficacy of nucleoside analog therapies.
- Potent dCK inhibition with low-nanomolar EC50.
- Orally bioavailable and metabolically stable for in vivo studies.
- Demonstrated antitumor activity in preclinical tumor models.
- Enhances efficacy of nucleoside analog therapies in combination studies.
- Supplied as a stable powder, soluble in DMSO for assay preparation.
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![Medchemexpress LLC 3-[2,4-dimethyl-5-[(Z)-(2-oxo-1H-indol-3-ylidene)methyl]-1H-pyrrol-3-yl]propanoic acid | 210644-62-5 | MFCD09743433 | 99.4% | 310.35 | C18H18N2O3 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000242440.png-250.jpg)
Medchemexpress LLC 3-[2,4-dimethyl-5-[(Z)-(2-oxo-1H-indol-3-ylidene)methyl]-1H-pyrrol-3-yl]propanoic acid | 210644-62-5 | MFCD09743433 | 99.4% | 310.35 | C18H18N2O3 | 50 MG
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Orantinib is a Z-isomer small-molecule tyrosine kinase inhibitor that targets VEGFR (Flk-1/KDR), PDGFRβ, and FGFR1. Supplied as an orange-red powder for research use, it is used in preclinical studies of angiogenesis and receptor tyrosine kinase signaling. Molecular formula C18H18N2O3; molecular weight 310.35; CAS 210644-62-5.
- Inhibits VEGFR, PDGFRβ, and FGFR1 for angiogenesis research.
- Orally active small-molecule inhibitor suitable for cell and biochemical assays.
- High reported purity supports reproducible experimental results.
- Solid powder form with defined storage conditions for long-term stability.
- Available in multiple pack sizes to support varied study scales.
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Medchemexpress LLC Rapamycin (sirolimus) | 53123-88-9 | MFCD00867594 | 99.9% | 914.17 g/mol | C51H79NO13 | 50 G
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Rapamycin (sirolimus) is a macrolide lactone that binds FKBP12 and acts as a potent, selective allosteric inhibitor of mTORC1. It is used in research to modulate autophagy, study mTOR signaling, and as a biochemical standard in cellular and molecular assays.
- High purity: 99.9% (HPLC)
- Molecular weight: 914.17 g/mol
- Chemical formula: C51H79NO13
- Function: mTOR inhibitor and autophagy activator for cell-based studies
- Form: supplied as a solid suitable for dissolution and formulation
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Medchemexpress LLC HY-15869 5mg Medchemexpress, Inauhzin CAS:309271-94-1 Purity:>98%
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Medchemexpress, HY-15869 5mg Inauhzin CAS:309271-94-1 Inauhzin is a dual SirT1/IMPDH2 inhibitor, and acts as an activator p53, used in the research of cancer. 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-101426 5mg Medchemexpress, RG14620 CAS:136831-49-7 Purity:>98%
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Medchemexpress, HY-101426 5mg RG14620 CAS:136831-49-7 RG14620 is an EGFR inhibitor with an IC 50 of 3 μM. 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 Fosmidomycin sodium salt | 66508-37-0 | 99.7% | 205.08 | 10 MG
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Fosmidomycin sodium salt is a phosphonic acid antibiotic and an antimalarial agent. It is active against both Gram-negative and Gram-positive bacteria.
- Phosphonic acid antibiotic
- Antimalarial agent
- Active against Gram-negative bacteria
- Active against Gram-positive bacteria
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Medchemexpress LLC Clindamycin phosphate | 24729-96-2 | MFCD11982855 | 98.0% | 1 G
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Clindamycin phosphate is a broad-spectrum bacteriostatic lincosamide antibiotic. It acts as a proagent, converting in vivo to the active form, Clindamycin, through phosphatase ester hydrolysis. This compound is used in research for conditions such as acne and bacterial vaginosis, demonstrating no cytotoxicity. Its antimicrobial properties are enhanced when combined with platelet rich fibrin (PRF).
- Acts as a broad-spectrum bacteriostatic lincosamide antibiotic.
- Converts to active Clindamycin in vivo.
- Shows no cytotoxicity.
- Enhances antimicrobial properties when combined with platelet rich fibrin.
- Suitable for research and analytical applications.
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