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HomeProduct name listDEMECOLCINE

DEMECOLCINE

Synonym(s):Colcemid - CAS 477-30-5 - Calbiochem;Colcemid solution;Demecolcine;N-Deacetyl-N-methylcolchicine;N-Deacetyl-N-methylcolchicine solution

  • CAS NO.:477-30-5
  • Empirical Formula: C21H25NO5
  • Molecular Weight: 371.43
  • MDL number: MFCD00075459
  • EINECS: 207-514-6
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-11-04 20:04:50
DEMECOLCINE Structural

What is DEMECOLCINE?

Description

Colcemid is a colchicine derivative that inhibits tubulin polymerization as potently as colchicine (IC50 = 2.1 and 2.4 μM, respectively) but is less toxic. At very low (nanomolar) concentrations, colcemid suppresses microtubule dynamicity and inhibits cell migration, while at micromolar levels it blocks microtubule assembly, arresting cells in metaphase. Mitotic block by colcemid is used to synchronize cells and for karyotyping in cytogenetic studies. Prolonged exposure to colcemid can activate p53, leading to apoptosis.

Chemical properties

Faintly Yellow Crystalline Powder

The Uses of DEMECOLCINE

An antimitotic agent that disrupts microtubles by binding to tubulin and preventing its polymerization. Stimulates the intrinsic GTPase activity of tubulin. Induces apoptosis in several normal and tumor cell lines and activates the JNK/SAPK signaling pathway.

The Uses of DEMECOLCINE

Inhibitor of spindle fiber formation

The Uses of DEMECOLCINE

Cell synchronization agent; for chromosome visualization; to induce oocyte enucleation for somatic cell cloning.

What are the applications of Application

Colcemid is a cell synchronizing, depolymerizing, anti-tubulin agent also used to inhibit mitotic division.

Definition

ChEBI: A secondary amino compound that is (S)-colchicine in which the N-acetyl group is replaced by an N-methyl group. Isolable from the autumn crocus, Colchicum autumnale, it is less toxic than olchicine and is used as an antineoplastic.

General Description

Colcemid is also known as demecolcine. Its generic name is N-methyl-N-deacetyl-colchicine. Colcemid depolymerizes microtubules and blocks mitosis at metaphase.

Biochem/physiol Actions

Often in karyotyping and cell cycle research it is desirable to increase the yield of mitotic cells in a particular phase of the cell cycle. This can be achieved in a variety of ways with the most popular being the use of a cell cycle synchronizing agent such as demecolcine. Demecolcine will arrest cells in metaphase with no remarkable effect on the biochemical events in mitotic cells or in synchronized G1 and S phase cells. White blood cells are often treated with demecolcine to arrest cells in metaphase.

Safety Profile

Poison by ingestion, intraperitoneal, parenteral, intravenous, and intramuscular routes. Human systemic effects by ingestion: (skin and appendages) hair effects. Human mutation data reported. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx.

Purification Methods

Colcemide is purified by chromatography on silica and eluting with CHCl3/MeOH (9:1), and by recrystallisation from EtOAc/Et2O to form yellow prisms. UV in EtOH has max 243nm ( 30,200) and 350nm ( 16,3000). [Synthesis, IR, NMR, MS: Capraro & Brossi Helv Chim Acta 62 965 1979, Beilstein 8 IV 3319.]

Properties of DEMECOLCINE

Melting point: 73-75°C
Boiling point: 501.11°C (rough estimate)
alpha  D20 -129.0° (c = 1 in chloroform)
Density  1.2350 (rough estimate)
refractive index  1.5614 (estimate)
storage temp.  2-8°C
solubility  DMSO: 10 mg/mL
form  powder
pka 8.48±0.40(Predicted)
color  White to off-white
Sensitive  Air & Light Sensitive
BRN  2822892
Stability: Hygroscopic

Safety information for DEMECOLCINE

Signal word Danger
Pictogram(s)
ghs
Skull and Crossbones
Acute Toxicity
GHS06
GHS Hazard Statements H300:Acute toxicity,oral
Precautionary Statement Codes P264:Wash hands thoroughly after handling.
P264:Wash skin thouroughly after handling.
P301+P310:IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

Computed Descriptors for DEMECOLCINE

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