2017
DOI: 10.20959/wjpps20176-9284
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Cordyceps, an Endangered Medicinal Plant: A Short Review

Abstract: Cordyceps is a genus of a fungi (sac fungi) that includes about 400 species. All Cordyceps species are endoparasitoids, parasitic mainly on insects and other arthropods (they are thus entomopathogenic In 2007, nuclear DNA sampling revealed this species to be unrelated to most of the rest of the members of the genus; as a result it was renamed Ophiocordyceps sinensis and placed in a new family, the Ophiocordycipitaceae.The generic name Cordyceps is derived from the Greek word kordyle, meaning "club", and the La… Show more

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“…After careful consideration, we decided to follow the synthetic route developed by Meier et al (Scheme 1). 48 Briefly, adenosine (2) was first converted into 9-(2,3-anhydro-β-D-ribofuranosyl)adenine (3) with a 98% yield. Then, metal hydride-mediated reductive opening of the epoxide ring in 3 afforded cordycepin (1) as the only regioisomer with a 95% yield.…”
Section: ■ Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…After careful consideration, we decided to follow the synthetic route developed by Meier et al (Scheme 1). 48 Briefly, adenosine (2) was first converted into 9-(2,3-anhydro-β-D-ribofuranosyl)adenine (3) with a 98% yield. Then, metal hydride-mediated reductive opening of the epoxide ring in 3 afforded cordycepin (1) as the only regioisomer with a 95% yield.…”
Section: ■ Introductionmentioning
confidence: 99%
“…3′-Deoxyadenosine (3′-dA, cordycepin, 1 ) (Figure ) is the main bioactive component isolated from the fermented broth of Cordyceps militaris, which is a medicinal parasitic fungus. This fungus has been used in traditional Chinese medicine for over 300 years as a treatment for inflammatory diseases and cancer. 3′-dA is a nucleoside analogue similar in structure to adenosine but lacking the 3′-hydroxyl group on the ribose moiety, and it has been proposed as an anticancer drug due to its numerous biological and pharmacological actions including inhibition of cell proliferation, induction of apoptosis, antimetastatic effect, and immune system activation . The mechanism of its antitumor activity is not well understood, but 3′-dA has been shown to regulate several signaling pathways associated with tumor growth and metastasis. , 3′-dA is thought to enter cells via the human equilibrative nucleoside transporters (hENT1), and to be phosphorylated by adenosine kinase (AK) to 3′-deoxyadenosine monophosphate (3′-dAMP).…”
Section: Introductionmentioning
confidence: 99%