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Colchicine

pharmaceutical raw materials
Colchicine structure

Colchicine 

structure
  • CAS No:

    64-86-8

  • Formula:

    C22H25NO6

  • Chemical Name:

    Colchicine

  • Synonyms:

    Acetamide,N-[(7S)-5,6,7,9-tetrahydro-1,2,3,10-tetramethoxy-9-oxobenzo[a]heptalen-7-yl]-;Colchicine;Acetamide,N-(5,6,7,9-tetrahydro-1,2,3,10-tetramethoxy-9-oxobenzo[a]heptalen-7-yl)-,(S)-;Benzo[a]heptalene,acetamide deriv.;N-[(7S)-5,6,7,9-Tetrahydro-1,2,3,10-tetramethoxy-9-oxobenzo[a]heptalen-7-yl]acetamide;NSC 757;(S)-N-(5,6,7,9-Tetrahydro-1,2,3,10-tetramethoxy-9-oxobenzo[a]heptalen-7-yl)acetamide;Colchineos;Colchisol;Colcin;Colsaloid;Condylon;(-)-Colchicine;Colcrys;(S)-N-(1,2,3,10-Tetramethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl)acetamide;Mitigare;5843-86-7;30512-31-3

  • Categories:

    Active Pharmaceutical Ingredients  >  Antineoplastic Agents

Description

Colchicine is a tubulin inhibitor and a microtubule disrupting agent. Colchicine inhibits microtubule polymerization with an IC50 of 3 nM.

Colchicine Basic Attributes

399.43700

399.44

200-598-5

29399990

Characteristics

83.09000

3.26250

Colchicine appears as odorless or nearly odorless pale yellow needles or powder that darkens on exposure to light. Used to treat gouty arthritis, pseudogout, sarcoidal arthritis and calcific tendinitis. (EPA, 1998)

1.32 g/cm3

142-150 °C

726.0±60.0 °C at 760 mmHg

392.9ºC

1.584

H2O: 45 g/L (20 ºC)

Poison room

3.2X10-11 mm Hg at 25 °C (est)

LD50 in rats (mg/kg): 1.6 i.v. (Rosenbloom, Ferguson); in mice (mg/kg): 4.13 i.v. (Beliles)

Specific optical rotation: -429 at 17 °C/D (water, 1.72%); -121 deg at 17 °C/d (concentration by volume = 0.9 g in 100 ml chloroform); max absorption (95% ethanol): 350.5 nm (log epsilon = 4.22), 243 nm (log epsilon = 4.47)

Odorless or nearly so

pH of 0.5% solution: 5.9

12.36None

Safety Information

I

6.1

UN 1544

3

R26/28

S13-S45

GH0700000

T+

Stable. Light sensitive. Incompatible with strong oxidizing agents.

Missing Phrase - N15.00950417-P201-P280-P304 + P340 + P310-P305 + P351 + P338 + P310-P308 + P313

H300 + H330-H318-H340

Colchicine Use and Manufacturing

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 signal

Computed Properties

Molecular Weight:399.4
XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:399.16818752
Monoisotopic Mass:399.16818752
Topological Polar Surface Area:83.1
Heavy Atom Count:29
Complexity:740
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Extract from the above information

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • DR WILLMAR SCHWABE INDIA PVT LTD

    United States United States
    Active
  • INDENA SPA

    France France
    Active
  • Nanjing Belger Pharmaceutical Technology Co., Ltd.

    China China
    Active

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