Decarbonylation colchicine
97%
- Product Code: 67765
Alias:
N-deacetyl-N-methylcolchicine; decarboxycolchicine; colchamide colchicine; decarbocolchicine; decarboxycolchicine (>98%, BR); N-deacetyl-N - Methylcolchicine solution; Demethacin solution
CAS:
477-30-5
Properties:
DMSO: 10 mg/mL
| Molecular Weight: | 371.43 g./mol | Molecular Formula: | C₂₁H₂₅NO₅ |
|---|---|---|---|
| EC Number: | 207-514-6 | MDL Number: | MFCD00075459 |
| Melting Point: | 73-75℃ | Boiling Point: | 501.11℃ (rough estimate) |
| Density: | 1.235 g/ml (rough estimate) | Storage Condition: | 2-8°C, inert gas, protected from light |
Product Description:
Decarbonylation colchicine is primarily utilized in research settings to study its effects on cellular processes, particularly in the context of microtubule dynamics. It serves as a valuable tool for investigating the mechanisms of cell division and the role of microtubules in maintaining cell structure and function. Researchers often employ it to explore its potential in inhibiting mitosis, which can provide insights into cancer therapy development. Additionally, it is used in biochemical studies to understand the interaction between colchicine derivatives and tubulin, aiding in the design of more effective therapeutic agents. Its application is largely confined to experimental and preclinical studies, contributing to advancements in cell biology and pharmacology.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | light yellow powder |
| PURITY | 96.5-100 |
| Loss on drying | 0 3.0% |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | Ft303,829.85 |
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Decarbonylation colchicine
Decarbonylation colchicine is primarily utilized in research settings to study its effects on cellular processes, particularly in the context of microtubule dynamics. It serves as a valuable tool for investigating the mechanisms of cell division and the role of microtubules in maintaining cell structure and function. Researchers often employ it to explore its potential in inhibiting mitosis, which can provide insights into cancer therapy development. Additionally, it is used in biochemical studies to understand the interaction between colchicine derivatives and tubulin, aiding in the design of more effective therapeutic agents. Its application is largely confined to experimental and preclinical studies, contributing to advancements in cell biology and pharmacology.
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