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Vindoline

 
ALX-350-102-M100 100 mg 153.00 USD
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Lacks physiological activity itself, but is contained as the pentacyclic moiety in the antineoplastic agents vinblastine and vincristine.

Product Details

Alternative Name:(2β,3β,4β,5α,12β,19α)-4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-Aspidospermidine-3-carboxylic acid methyl ester
 
Formula:C25H32N2O6
 
MW:456.5
 
Source:Isolated from Catharanthus roseus.
 
CAS:2182-14-1
 
MI:14: 9988
 
RTECS:CJ0120000
 
Purity:≥90% (assay on dried basis)
 
Appearance:White to off-white crystalline powder.
 
Solubility:Soluble in 100% ethanol and water (30mg/ml).
 
Shipping:Ambient Temperature
 
Long Term Storage:-20°C
 
Handling:Very hygroscopic.
 
Regulatory Status:RUO - Research Use Only
 
350-102
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350-102

Product Literature References

Catharanthus roseus L. plants and explants infected with phytoplasmas: alkaloid production and structural observations: M.A. Favali, et al.; Protoplasma 223, 45 (2004), Abstract;
Antimitotic agents: chemistry and recognition of tubulin molecule: S. Iwasaki; Med. Res. Rev. 13, 183 (1993), Abstract;
Mechanism of interaction of vinca alkaloids with tubulin: catharanthine and vindoline: V. Prakash & S.N. Timasheff; Biochemistry 30, 873 (1991), Abstract;
Photochemical one-pot synthesis of vinblastine and vincristine: S. Pennanen & A. Huhtikangas; Photochem. Photobiol. 51, 515 (1990), Abstract;

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Vinblastine . sulfate 

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Catharanthine . tartrate 

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