COLCHICINE

Colchicine disrupts microtubule formation, reducing inflammation in gout and familial Mediterranean fever. Side effects include diarrhea, abdominal pain, and bone marrow suppression. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 73ba2899c9f4 Category: Tag:

Product Description


Mechanism of Action

Colchicine is a microtubulepolymerization inhibitor that binds tubulin, preventing formation of the mitotic spindle. This disrupts neutrophil chemotaxis, inflammasome activation (particularly NLRP3), and cytokine release. Its powerful antiinflammatory activity stems from inhibition of microtubuledependent cell migration and intracellular trafficking.

Benefits and Advantages

Used in goutpathophysiology modelling, tubulinbinding research, inflammasome inhibition studies, mitosisdisruption assays, and autoinflammatorydisease investigations.

Side Effects and Risks

Risks include GI toxicity, myelosuppression, neuromyopathy, hepatotoxicity and multiorgan dysfunction at high concentrations. Handle as a potent tubulindisrupting agent.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C22H25NO6

Molecular Weight

399.4 g/mol

CAS Number

64-86-8

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

greater than or equal to 100 mg/mL at 70 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

colchicine; 64-86-8; Colchisol; Colchineos; Colchicinum

IUPAC/Chemical Name

N-[(7S)-1,2,3,10-tetramethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide

InChl Key

IAKHMKGGTNLKSZ-INIZCTEOSA-N

InChl Code

InChI=1S/C22H25NO6/c1-12(24)23-16-8-6-13-10-19(27-3)21(28-4)22(29-5)20(13)14-7-9-18(26-2)17(25)11-15(14)16/h7,9-11,16H,6,8H2,1-5H3,(H,23,24)/t16-/m0/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/6167;

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