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Submit ReviewColchicine
Description: Inhibitor of tubulin
Chemical Name: (S)-N-(5,6,7,9-Tetrahydro-1,2,3,10-tetramethoxy-9-oxobenzo[a]heptalen-7-yl)acetamide
Purity: ≥98% (HPLC)
Biological Activity for Colchicine
Colchicine is a plant-derived alkaloid that binds to tubulin and depolymerizes microtubules. Identified as a candidate for repurposing for COVID-19. Inhibits NLRP3 inflammasomes. Also decreases TNF-α receptor expression and reduces cytokine levels in macrophages. Anti-inflammatory.
Technical Data for Colchicine
| M. Wt | 399.44 |
| Formula | C22H25NO6 |
| Storage | Store at RT |
| Purity | ≥98% (HPLC) |
| CAS Number | 64-86-8 |
| PubChem ID | 2833 |
| InChI Key | IAKHMKGGTNLKSZ-UHFFFAOYSA-N |
| Smiles | COC1=C(OC)C(OC)=C2C(CCC(NC(C)=O)C3=CC(=O)C(OC)=CC=C23)=C1 |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Solubility Data for Colchicine
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| water | 39.94 | 100 | |
| DMSO | 39.94 | 100 |
Preparing Stock Solutions for Colchicine
The following data is based on the product molecular weight 399.44. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.5 mL | 12.52 mL | 25.04 mL |
| 5 mM | 0.5 mL | 2.5 mL | 5.01 mL |
| 10 mM | 0.25 mL | 1.25 mL | 2.5 mL |
| 50 mM | 0.05 mL | 0.25 mL | 0.5 mL |
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Product Datasheets for Colchicine
References for Colchicine
References are publications that support the biological activity of the product.
Bai et al (1996) Identification of cysteine 354 of β-tubulin as part of the binding site for the A ring of colch. J.Biol.Chem. 271 12639 PMID: 8647876
Burns (1992) Analysis of the colchicine-binding site of β-tubulin. FEBS Lett. 297 205 PMID: 1544399
Hastie (1991) Interactions of colch. with tubulin. Pharmacol.Ther. 51 377 PMID: 1792241
Morselli et al (2021) Network medicine framework for identifying drug repurposing opportunities for COVID-19. Proc.Nat.Acad.Sci.U.S.A. 118 PMID: 33906951
Ribeiro et al (2020) The therapeutic potential of colch in the complications of COVID19. Could the immunometabolic properties of an old and cheap drug help? Metabol.Open 7 100045 PMID: 32808940
Martinez et al (2018) The NLRP3 inflammasome and the emerging role of colch to inhibit atherosclerosis-associated inflammation. Atherosclerosis 269 262 PMID: 29352570
If you know of a relevant reference for Colchicine, please let us know.
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Keywords: Colchicine, Colchicine supplier, inhibitors, inhibits, tubulin, Tau, Tubulin, Microtubules, Mitosis, COVID-19, SARS-CoV-2, severe, acute, respiratory, syndrome, inflammasome, NLRP3, Inflammasomes, 1364, Tocris Bioscience
⚠ WARNING: This product can expose you to chemicals including Colchicine, which is known to the State of California to cause reproductive toxicity with developmental effects. For more information, go to www.P65Warnings.ca.gov
5 Citations for Colchicine
Citations are publications that use Tocris products. Selected citations for Colchicine include:
Khan et al (2016) Genetic screening reveals a link between Wnt signaling and antitubulin drugs. Pharmacogenomics J 16 164 PMID: 26149735
Park et al (2016) Pyrin inflammasome activation and RhoA signaling in the autoinflammatory diseases FMF and HIDS. Nat Immunol 17 914 PMID: 27270401
Melemedjian et al (2014) Local translation and retrograde axonal transport of CREB regulates IL-6-induced nociceptive plasticity. Mol Pain 10 45 PMID: 24993495
Kathawala et al (2015) The small molecule tyrosine kinase inhibitor NVP-BHG712 antagonizes ABCC10-mediated PacT. resistance: a preclinical and pharmacokinetic study. Oncotarget 6 510 PMID: 25402202
Zhang (2017) The BTK Inhibitor, Ibrutinib (PCI-32765) Overcomes PacT. Resistance in ABCB1 and ABCC10 Overexpressing Cells and Tumors. Mol Cancer Ther 16 1021 PMID: 28265007
Do you know of a great paper that uses Colchicine from Tocris? Please let us know.
Reviews for Colchicine
Average Rating: 5 (Based on 1 Review.)
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Paclitaxel, docetaxel, vincristine, vinblastine, colchicine, cisplatin, and mitoxantrone screen for Human epidermal carcinoma.
By
Anonymous on 11/17/2019
Assay Type: In Vitro
Species: Human
Cell Line/Tissue: Human epidermal carcinoma cell line
Human epidermal carcinoma cell line was treated with Paclitaxel, docetaxel,vincristine, vinblastine, colchicine, cisplatin, and mitoxantrone which purchased from Tocris Bioscience.
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Cell Cycle and DNA Damage Research Product Guide
This product guide provides a review of the cell cycle and DNA damage research area and lists over 150 products, including research tools for:
- Cell Cycle and Mitosis
- DNA Damage Repair
- Targeted Protein Degradation
- Ubiquitin Proteasome Pathway
- Chemotherapy Targets