CAS 6901-13-9
:Lumicolchicine
Description:
Lumicolchicine, with the CAS number 6901-13-9, is a synthetic derivative of colchicine, a well-known alkaloid derived from the plant Colchicum autumnale. This compound exhibits characteristics similar to colchicine, primarily functioning as a microtubule inhibitor, which interferes with cell division by disrupting the mitotic spindle formation. Lumicolchicine is notable for its potential applications in cancer research and treatment, as it can induce apoptosis in rapidly dividing cells. The compound is typically characterized by its low solubility in water, which can affect its bioavailability and pharmacokinetics. Additionally, lumicolchicine has been studied for its effects on various cellular processes, including inflammation and cell signaling pathways. Safety and toxicity profiles are essential considerations in its application, as with many alkaloids, due to potential side effects. Overall, lumicolchicine represents a significant area of interest in medicinal chemistry, particularly in the development of targeted therapies for malignancies.
Formula:C22H25NO6
InChI:InChI=1/C22H25NO6/c1-10(24)23-13-7-6-11-8-15(27-3)21(28-4)22(29-5)16(11)17-12-9-14(26-2)20(25)18(12)19(13)17/h8-9,12-13,18H,6-7H2,1-5H3,(H,23,24)/t12?,13-,18?/m0/s1
InChI key:InChIKey=VKPVZFOUXUQJMW-FHSNZYRGSA-N
SMILES:N(C(C)=O)[C@@H]1C2=C([C@@]3([C@]2(C(=O)C(OC)=C3)[H])[H])C=4C(=CC(OC)=C(OC)C4OC)CC1
Synonyms:- (-)-β-Lumicolchicine
- (7S-(7alpha,7bbeta,10abeta))-N-(5,6,7,7b,8,10a-Hexahydro-1,2,3,9-tetramethoxy-8-oxobenzo(a)cyclopenta(3,4)cyclobuta(1,2-c)cyclohepten-7-yl)acetamide
- Acetamide, N-(5,6,7,7b,8,10a-hexahydro-1,2,3,9-tetramethoxy-8-oxobenzo[a]cyclopenta[3,4]cyclobuta[1,2-c]cyclohepten-7-yl)-, [7S-(7α,7bβ,10aβ)]-
- Acetamide, N-[(7S,7bR,10aS)-5,6,7,7b,8,10a-hexahydro-1,2,3,9-tetramethoxy-8-oxobenzo[a]cyclopenta[3,4]cyclobuta[1,2-c]cyclohepten-7-yl]-
- Benzo[a]cyclopenta[3,4]cyclobuta[1,2-c]cycloheptene, acetamide deriv.
- Lumicolchicine
- Lumicolchicine (9CI)
- N-(1,2,3,9-tetramethoxy-8-oxo-5,6,7,7b,8,10a-hexahydrobenzo[a]cyclopenta[3,4]cyclobuta[1,2-c][7]annulen-7-yl)acetamide
- N-[(7R,7bS,10aR)-1,2,3,9-tetramethoxy-8-oxo-5,6,7,7b,8,10a-hexahydrobenzo[a]cyclopenta[3,4]cyclobuta[1,2-c][7]annulen-7-yl]acetamide
- N-[(7S,7bR,10aS)-1,2,3,9-tetramethoxy-8-oxo-5,6,7,7b,8,10a-hexahydrobenzo[a]cyclopenta[3,4]cyclobuta[1,2-c][7]annulen-7-yl]acetamide
- N-[(7S,7bR,10aS)-5,6,7,7b,8,10a-Hexahydro-1,2,3,9-tetramethoxy-8-oxobenzo[a]cyclopenta[3,4]cyclobuta[1,2-c]cyclohepten-7-yl]acetamide
- Nsc 221661
- Nsc 56233
- β-Lumi-(-)-colchicine
- Colchicine EP Impurity C
- N-[(7S)-5,6,7,7bβ,8,10aβ-Hexahydro-1,2,3,9-tetramethoxy-8-oxobenzo[a]cyclopenta[3,4]cyclobuta[1,2-c]cyclohepten-7-yl]acetamide
- N-[(7S,7bR,10aS)-1,2,3,9-Tetramethoxy-8-oxo-5,6,7,7b,8,10a-hexahydrobenzo[a]cyclopenta[3,4]cyclobuta[1,2-c]cyclohepten-7-yl]acetamide (β-Lumicolchicine)
- N-[(7S,7bR,10aS)-1,2,3,9-Tetrametho
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Found 6 products.
Lumicolchicine
CAS:Lumicolchicine is a bioactive chemical.Formula:C22H25NO6Color and Shape:SolidMolecular weight:399.44β-Lumi (-)-Colchicine
CAS:<p>Applications An analog of Colchicine (C640000), β-lumicolchicine, does not bind tubulin or disrupt microtubules. A GABAA receptor chloride channel.<br>References Andreu, J., et al.: Biochemistry, 37, 8356 (1998), Weiner, J., et al.: J. Pharmacol. Exp. Ther., 284, 95 (1998), Hong, G., et al.: J. Pharm. Sci., 88, 147 (1999),<br></p>Formula:C22H25NO6Color and Shape:NeatMolecular weight:399.44(-)-beta-Lumicolchicine
CAS:<p>(-)-beta-Lumicolchicine is a cytosolic Ca2+ ionophore that binds to the gamma-aminobutyric acid receptor. It has been shown to inhibit the activity of actin filaments and inhibit cellular organelle movement. (-)-beta-Lumicolchicine is also an activator of protein kinase C, which may be clinically relevant.</p>Formula:C22H25NO6Purity:Min. 95%Molecular weight:399.44 g/mol





