Decarbonylation colchicine
97%
Reagent
Code: #67765
Alias
N-deacetyl-N-methylcolchicine; decarboxycolchicine; colchamide colchicine; decarbocolchicine; decarboxycolchicine (>98%, BR); N-deacetyl-N - Methylcolchicine solution; Demethacin solution
CAS Number
477-30-5
Properties
DMSO: 10 mg/mL
blur_circular Chemical Specifications
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Molecular Information
Weight
371.43 g/mol
Formula
C₂₁H₂₅NO₅
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Registry Numbers
EC Number
207-514-6
MDL Number
MFCD00075459
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Physical Properties
Melting Point
73-75℃
Boiling Point
501.11℃ (rough estimate)
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Storage & Handling
Density
1.235 g/ml (rough estimate)
Storage
2-8°C, inert gas, protected from light
description 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.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | light yellow powder |
Purity | 96.5-100 |
Loss on Drying | 0-3.0% |
Infrared Spectrum | Conforms to Structure |
shopping_cart Available Sizes & Pricing
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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