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Synthesis and antitumour activity of derivatives of curdlan and lichenan branched at C-6

Demleitner, S., Kraus, J. and Franz, Gerhard (1992) Synthesis and antitumour activity of derivatives of curdlan and lichenan branched at C-6. Carbohydrate research 226 (2), pp. 239-246.

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Abstract

Derivatives of curdlan and lichenan, linear (1----3)-beta-D- and (1----3/1----4)-beta-D-glucans, respectively, have been synthesised having alpha-L-arabinofuranosyl, alpha-L-rhamnosyl, beta-D-glucosyl, and beta-gentiobiosyl side chains attached at positions 6. These water-soluble derivatives, obtained by condensation of the 2,4- and 2,4-/2,3-di-O-phenylcarbamoyl derivatives of curdlan and ...

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Item type:Article
Date:1992
Institutions:Chemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Franz
Identification Number:
ValueType
1617687PubMed ID
Classification:
NotationType
AnimalsMESH
Antineoplastic AgentsMESH
FemaleMESH
Glucans/pharmacologyMESH
MiceMESH
Sarcoma 180/drug therapyMESH
beta-GlucansMESH
Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Unknown
Item ID:22623
Owner only: item control page
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