CM10
100mg
| ≥99%
CSNpharm
CM10
10mg
| ≥99%
CSNpharm
CM10
50mg
| ≥99%
CSNpharm
CNQX
10mg
| ≥98%
CSNpharm
CNQX
100mg
| ≥98%
CSNpharm
CNQX
25mg
| ≥98%
CSNpharm
CNQX
50mg
| ≥98%
CSNpharm
CNQX
5mg
| ≥98%
CSNpharm
CSNpharm
Coelenterazineis is the substrate of many luciferases, as a luciferin, light-emitting molecules, found in many aquatic organisms across eight phyla.
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Coelenterazineis is the substrate of many luciferases, as a luciferin, light-emitting molecules, found in many aquatic organisms across eight phyla.
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CSNpharm
Coelenterazineis is the substrate of many luciferases, as a luciferin, light-emitting molecules, found in many aquatic organisms across eight phyla.
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CSNpharm
Coelenterazineis is the substrate of many luciferases, as a luciferin, light-emitting molecules, found in many aquatic organisms across eight phyla.
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CSNpharm
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COH000 is an irreversible inhibitor of ubiquitin-like 1-activating enzyme (SUMO-activating enzyme) with IC50 of 0.2 μM for SUMOylation in vitro.
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COH000 is an irreversible inhibitor of ubiquitin-like 1-activating enzyme (SUMO-activating enzyme) with IC50 of 0.2 μM for SUMOylation in vitro.
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CSNpharm
COH000 is an irreversible inhibitor of ubiquitin-like 1-activating enzyme (SUMO-activating enzyme) with IC50 of 0.2 μM for SUMOylation in vitro.
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CSNpharm
COH000 is an irreversible inhibitor of ubiquitin-like 1-activating enzyme (SUMO-activating enzyme) with IC50 of 0.2 μM for SUMOylation in vitro.
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CSNpharm
COH000 is an irreversible inhibitor of ubiquitin-like 1-activating enzyme (SUMO-activating enzyme) with IC50 of 0.2 μM for SUMOylation in vitro.
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CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
Colimycin Sulfate is an antibiotic produced by certain strains of the bacteria Paenibacillus polymyxa, which can bind to lipids on the cell cytoplasmic membrane of Gram-negative bacteria and disrupts the cell wall integrity.
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CSNpharm
Colimycin Sulfate is an antibiotic produced by certain strains of the bacteria Paenibacillus polymyxa, which can bind to lipids on the cell cytoplasmic membrane of Gram-negative bacteria and disrupts the cell wall integrity.
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CSNpharm
Columbamine is a quaternary isoquinoline alkaloid isolated and purified from the roots of Coptis chinensis Franch, shows strong activity with IC50 48.1 µM and exerts anti-proliferative and anti-vasculogenic effects on metastatic human osteosarcoma U2OS cells with low toxicity.
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CSNpharm
Columbamine is a quaternary isoquinoline alkaloid isolated and purified from the roots of Coptis chinensis Franch, shows strong activity with IC50 48.1 µM and exerts anti-proliferative and anti-vasculogenic effects on metastatic human osteosarcoma U2OS cells with low toxicity.
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CSNpharm
Columbamine is a quaternary isoquinoline alkaloid isolated and purified from the roots of Coptis chinensis Franch, shows strong activity with IC50 48.1 µM and exerts anti-proliferative and anti-vasculogenic effects on metastatic human osteosarcoma U2OS cells with low toxicity.
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CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
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CSNpharm
Compstatin is a complement inhibitor which can bind C3 inhibiting proteolytic cleavage by C3 convertase with IC50 value of 28 μM and activate classical and alternative complement pathways with IC50 values of 63 and 12 μM, respectively.
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CSNpharm
Compstatin is a complement inhibitor which can bind C3 inhibiting proteolytic cleavage by C3 convertase with IC50 value of 28 μM and activate classical and alternative complement pathways with IC50 values of 63 and 12 μM, respectively.
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CSNpharm
CSNpharm
CSNpharm
CSNpharm
Congo Red
250mg
| Purity Not Available
CSNpharm
Congo Red is an azo dye. Congo Red (CR) binding been used as a diagnostic test for the presence of amyloid in tissue sections.
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Coniferaldehyde, a natural product isolated and purified from the herbs of Artemisia annua L., shows the most effective increase of HSF1 and induced successive expressions of HSP27 and HSP70 in a dose-dependent manner without cellular cytotoxicity, suggesting a possible application as a HSP inducer to act as cytoprotective agent.
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CSNpharm
Coniferaldehyde, a natural product isolated and purified from the herbs of Artemisia annua L., shows the most effective increase of HSF1 and induced successive expressions of HSP27 and HSP70 in a dose-dependent manner without cellular cytotoxicity, suggesting a possible application as a HSP inducer to act as cytoprotective agent.
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