ChemicalBook >> CAS DataBase List >>DEMECOLCINE

DEMECOLCINE

CAS No.
477-30-5
Chemical Name:
DEMECOLCINE
Synonyms
COLCEMID;COLCHAMINE;omaine;Colcemide;Tropisteron;(S)-1,2,3,10-Tetramethoxy-7-(methylamino)-6,7-dihydrobenzo[a]heptalen-9(5H)-one;omain;Osamin;C-12669;nsc3096
CBNumber:
CB3460085
Molecular Formula:
C21H25NO5
Molecular Weight:
371.43
MDL Number:
MFCD00075459
MOL File:
477-30-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-30 16:52:23

DEMECOLCINE Properties

Melting point 73-75°C
alpha D20 -129.0° (c = 1 in chloroform)
Boiling point 501.11°C (rough estimate)
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
InChI 1S/C21H25NO5/c1-22-15-8-6-12-10-18(25-3)20(26-4)21(27-5)19(12)13-7-9-17(24-2)16(23)11-14(13)15/h7,9-11,15,22H,6,8H2,1-5H3
InChIKey NNJPGOLRFBJNIW-UHFFFAOYSA-N
SMILES N(C1CCc2c(c(c(c(c2)OC)OC)OC)C3=CC=C(C(=O)C=C31)OC)C
FDA UNII Z01IVE25KI
ATC code L01CC01
UNSPSC Code 12352207
NACRES NA.75

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H300
Precautionary statements  P264-P301+P310
Hazard Codes  T,T+
Risk Statements  25-26/27/28
Safety Statements  22-24/25-45-36/37/39
RIDADR  UN 2811 6.1/PG 2
WGK Germany  3
RTECS  GH0800000
8-10-23
HazardClass  6.1(a)
PackingGroup  II
Toxicity LD50 oral in mouse: 25530ug/kg
NFPA 704
0
4 0

DEMECOLCINE price More Price(75)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich D1925 Demecolcine solution 10 μg/mL in HBSS, ACF Qualified, BioXtra 477-30-5 20ml $68.8 2026-04-30 Buy
Sigma-Aldrich 234109-M Colcemid - CAS 477-30-5 - Calbiochem Cell synchronization agent. 477-30-5 5mg $139 2026-04-30 Buy
Sigma-Aldrich 234109-M Colcemid Cell synchronization agent. 477-30-5 500 mg $4760 2026-04-30 Buy
Sigma-Aldrich 234109-M Colcemid Cell synchronization agent. 477-30-5 1 g $15460 2026-04-30 Buy
Sigma-Aldrich 234109-M Colcemid Cell synchronization agent. 477-30-5 10 mg $16040 2026-04-30 Buy
Product number Packaging Price Buy
D1925 20ml $68.8 Buy
234109-M 5mg $139 Buy
234109-M 500 mg $4760 Buy
234109-M 1 g $15460 Buy
234109-M 10 mg $16040 Buy

DEMECOLCINE Chemical Properties,Uses,Production

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

Uses

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.

Uses

Inhibitor of spindle fiber formation

Uses

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

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.]

References

[1] ANJUM MUZAFFAR. Antitubulin effects of derivatives of 3-demethylthiocolchicine, methylthio ethers of natural colchicinoids, and thioketones derived from thiocolchicine. Comparison with colchicinoids[J]. Journal of Medicinal Chemistry, 1990, 33 2: 567-571. DOI: 10.1021/jm00164a015
[2] C L RIEDER  R E P. Colcemid and the mitotic cycle.[J]. Journal of cell science, 1992, 102 ( Pt 3): 387-392. DOI: 10.1242/jcs.102.3.387
[3] MARY ANN JORDAN  Leslie W. Microtubules as a target for anticancer drugs[J]. Nature Reviews Cancer, 2004, 4 4: 253-265. DOI: 10.1038/nrc1317
[4] JOZEF CURLEJ  Peter C  Jozef Bulla. Occurrence of chromosomal aneuploidy in rabbit oocytes and embryos at different developmental stages.[J]. Zygote, 2010, 18 3: 203-207. DOI: 10.1017/s0967199409990207
[5] HAILING YANG F C Anutosh Ganguly. Inhibition of cell migration and cell division correlates with distinct effects of microtubule inhibiting drugs.[J]. The Journal of Biological Chemistry, 2010: 32242-32250. DOI: 10.1074/jbc.m110.160820
[6] JANE BAYANI  Jeremy A S. Preparation of Cytogenetic Specimens from Tissue Samples[J]. Current Protocols in Cell Biology, 2004, 23 1. DOI: 10.1002/0471143030.cb2202s23
[7] ANNA A SABLINA. p53 activation in response to microtubule disruption is mediated by integrin-Erk signaling[J]. Oncogene, 2001, 20 8: 899-909. DOI: 10.1038/sj.onc.1204156

DEMECOLCINE Preparation Products And Raw materials

Raw materials

Preparation Products

DEMECOLCINE Suppliers

Global( 150)Suppliers
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2110 70
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50
Sichuan Kulinan Technology Co., Ltd 400-1166-196 18981987031 cdhxsj@163.com China 11674 57
Dalian Meilun Biotech Co., Ltd. 0411-62910999 13889544652 sales@meilune.com China 4765 58
Hangzhou Sage Chemical Co., Ltd. +86057186818502 13588463833 info@sagechem.com China 10265 58
Beijing HuaMeiHuLiBiological Chemical 010-56205725 waley188@sohu.com China 12323 58
Guangzhou Isun Pharmaceutical Co., Ltd 020-39119399 18927568969 isunpharm@qq.com China 4773 55
Shanghai Macklin Biochemical Co.,Ltd. 15221275939 15221275939 shenlinxing@macklin.cn China 15775 55
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51389 80

View Lastest Price from DEMECOLCINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
	DEMECOLCINE pictures 2026-09-02 DEMECOLCINE
477-30-5
$1.00-8.00 1KG 99% Henan Fengda Chemical Co., Ltd
Colcemid pictures 2026-08-16 Colcemid
477-30-5
$31.00-156.00 99.65% 10g TargetMol Chemicals Inc.
DEMECOLCINE pictures 2026-08-07 DEMECOLCINE
477-30-5
$1.00-45.00 1KG 99% 420000KG Shaanxi Dideu Medichem Co. Ltd
  • 	DEMECOLCINE pictures
  • DEMECOLCINE
    477-30-5
  • $1.00-8.00
  • 99%
  • Henan Fengda Chemical Co., Ltd
  • Colcemid pictures
  • Colcemid
    477-30-5
  • $31.00-156.00
  • 99.65%
  • TargetMol Chemicals Inc.
  • DEMECOLCINE pictures
  • DEMECOLCINE
    477-30-5
  • $1.00-45.00
  • 99%
  • Shaanxi Dideu Medichem Co. Ltd

DEMECOLCINE Spectrum

substancef DEMECOLCINE HYBRI-MAXR DEMECOLCINE SOLUTION 10 UG/ML Colcemid-D3=Demecolcine-D3 N-Deacetyl-N-methyl(deutero)colchicine COLCEMIDE(R) COLCEMID(R) COLCHAMINE DEMECOLCIN DEMECOLCINE Benzoaheptalen-9(5H)-one, 6,7-dihydro-1,2,3,10-tetramethoxy-7-(methylamino)-, (7S)- COLCHICINE,N-DEACETYL-N-METHYL- DEMECOLCINE/COLCEMIDE/COLCHICINE N-Deacetyl-N-methylcolchicine, Colcemid ColcemidTM solution, N-Deacetyl-N-methylcolchicine solution Demecolcine solution C-12669 Osamin Demecolcine,N-Deacetyl-N-methylcolchicine Colcemid, Demecolcine (7S)-6,7-Dihydro-1,2,3,10-tetraMethoxy-7-(MethylaMino)-benzo[a]heptalen-9(5H)-one ColchaMin 6,7-dihydro-1,2,3,10-tetramethoxy-7-(methylamino)-benzo(alpha)heptalen-9(5h) 7-deacetamido-7-(methylamino)-colchicin alkaloidh3,fromcolchicumantumnale benzo(a)heptalen-9(5h)-one,6,7-dihydro-1,2,3,10-tetramethoxy-7-(methylamino) ciba12669a deacetylmethylcolchicine deacetyl-n-methyl-colchicin deacetyl-n-methylcolchicine desmecolcine kolchamin kolchicin n-deacetyl-n-methyl-colchicin n-desacetylmethylcolchicine n-methyl-n-desacetylcolchicine nsc3096 omain reichstein’sf santavy’ssubstancef N-DEACETYL-N-METHYLCOLCHICINE N-DESACETYL-N-METHYLCOLCHICINE N-METHYL-N-DEACETYL-COLCHICINE Colcemid - CAS 477-30-5 - Calbiochem Colchicine N-Methyl Analog (-)-demecolcine DEMECOLCINE USP/EP/BP Decarbonylation colchicine (S)-1,2,3,10-Tetramethoxy-7-(methylamino)-6,7-dihydrobenzo[a]heptalen-9(5H)-one Demecolcine, ≥98%+ Tropisetronum Colchicine Impurity 23 Demecolcine in methanol Chelidonine Impurity?3 Colcemid, 10 mM in DMSO Colcemide COLCEMID omaine