ChemInform Abstract: A Focused Sulfated Glycoconjugate Ugi Library for Probing Heparan Sulfate-Binding Angiogenic Growth Factors
Small molecule heparan sulfate mimetics like (VI) and (X) are synthesized by the Ugi four‐component condensation of mannopyranoside‐derived isocyanides (I) and (VII) with a variety of carboxylic acids, e.g.(II), amines such as (III) and (VIII), and formaldehyde (IV) as the carbonyl component, follow...
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Veröffentlicht in: | ChemInform 2013-02, Vol.44 (6), p.no-no |
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creator | Liu, Ligong Li, Caiping Cochran, Siska Feder, Daniel Guddat, Luke W. Ferro, Vito |
description | Small molecule heparan sulfate mimetics like (VI) and (X) are synthesized by the Ugi four‐component condensation of mannopyranoside‐derived isocyanides (I) and (VII) with a variety of carboxylic acids, e.g.(II), amines such as (III) and (VIII), and formaldehyde (IV) as the carbonyl component, followed by sulfonation. |
doi_str_mv | 10.1002/chin.201306150 |
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KGaA, Weinheim</rights><rights>Copyright © 2013 WILEY-VCH Verlag GmbH & Co. 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subjects | anticancer activity anticarcinogenic activity anticarcinogenic activity, anticancer activity carbohydrates Heparan sulfate multicomponent reactions |
title | ChemInform Abstract: A Focused Sulfated Glycoconjugate Ugi Library for Probing Heparan Sulfate-Binding Angiogenic Growth Factors |
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