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(R)-Colchicine is the R-isomer of Colchicine. Colchicine is an orally active alkaloid that serves as an effective microtubule protein inhibitor and disruptor. It inhibits microtubule polymerization with an IC50 of 3 nM and acts as a competitive antagonist of the α3 glycine receptor (GlyR). Additionally, Colchicine prevents NSAID-induced small intestinal injury by inhibiting the activation of the NLRP3 inflammasome. It exhibits extensive anti-inflammatory, immunosuppressive, and potent antifibrotic effects, with potential applications in gouty arthritis research.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | (R)-Colchicine is the R-isomer of Colchicine. Colchicine is an orally active alkaloid that serves as an effective microtubule protein inhibitor and disruptor. It inhibits microtubule polymerization with an IC50 of 3 nM and acts as a competitive antagonist of the α3 glycine receptor (GlyR). Additionally, Colchicine prevents NSAID-induced small intestinal injury by inhibiting the activation of the NLRP3 inflammasome. It exhibits extensive anti-inflammatory, immunosuppressive, and potent antifibrotic effects, with potential applications in gouty arthritis research. |
| Molecular Weight | 399.44 |
| Formula | C22H25NO6 |
| Cas No. | 75520-89-7 |
| Smiles | O(C)C1=C2C=3C([C@H](NC(C)=O)CCC2=CC(OC)=C1OC)=CC(=O)C(OC)=CC3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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