2010
DOI: 10.1016/j.ejmech.2010.02.002
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Synthesis and antitumor activity of new shikonin glycosides

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Cited by 53 publications
(26 citation statements)
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“…Several authors have investigated ShD‐mediated tumour suppression and its in vitro underlying mechanisms (Chang et al , ; Lee et al , ; Su et al , ; Yang et al , ; Yao and Zhou, ), including induction of apoptosis via the activation of signalling pathways involved in reactive oxygen species formation (Chang et al , ), p53, p27, Bcl‐2 or caspases (Hsu et al , ) and inhibition of tumour propagation via telomerase and DNA topoisomerase I/II blockade (Fujii et al , ). However, little is known about the in vivo effects of ShD on the immune function and immune organ morphology of mice bearing transplantable neoplasms.…”
Section: Introductionmentioning
confidence: 99%
“…Several authors have investigated ShD‐mediated tumour suppression and its in vitro underlying mechanisms (Chang et al , ; Lee et al , ; Su et al , ; Yang et al , ; Yao and Zhou, ), including induction of apoptosis via the activation of signalling pathways involved in reactive oxygen species formation (Chang et al , ), p53, p27, Bcl‐2 or caspases (Hsu et al , ) and inhibition of tumour propagation via telomerase and DNA topoisomerase I/II blockade (Fujii et al , ). However, little is known about the in vivo effects of ShD on the immune function and immune organ morphology of mice bearing transplantable neoplasms.…”
Section: Introductionmentioning
confidence: 99%
“…The 1-methyoxyl of 4a was acetylated in a mixture of acetic anhydride, acetic acid, and sulfuric acid (1:0.4:0.1), 14 and then converted to 1-hydroxyl by hydrazine acetate to give compound 6. 15 The glycosylation was hard to proceed due to the steric hindrance and low reactivity of the 5-hydroxyl group in compound 9. Two kinds of donor were used to study glycosylation reaction: the fluoro donor 7 and the trichloroacetimidate donor 8.…”
mentioning
confidence: 99%
“…Also, conjugation of naphthoquinones with carbohydrates led to the novel structures with new types of biological activity. [8][9][10][11] In the course of our drug research project we developed an effective method for preparation of naphthoquinone acetylthioglucosides by the condensation of available substituted chloroquinones 1a,b with tetra-O-acetyl-1-thio-β-D-glucopyranose (2) (AGSH) and obtained related naphthoquinone acetylglucosides 3a,b. The acetylglucoside naphthoquinones 3a,b readily were deacetylated with MeONa/MeOH and led the water soluble thioglucosides 4a,b.…”
Section: Introductionmentioning
confidence: 99%