Skip to search formSkip to main contentSkip to account menu
You are currently offline. Some features of the site may not work correctly.

ryanodol

National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
The pool of abundant chiral terpene building blocks (i.e., "chiral pool terpenes") has long served as a starting point for the… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
2017
2017
  • E. Prusov
  • Angewandte Chemie
  • 2017
  • Corpus ID: 45140562
Total syntheses of the tetracyclic terpene waihoensene and the densely functionalized tetracyclic compound ryanodol have recently… Expand
2016
2016
Ryanodane diterpenoids structurally share an extremely complex fused ring system, but differ in the substitution patterns of the… Expand
  • figure 2
Highly Cited
2014
Highly Cited
2014
Ryanodol (1) exists in nature in the form of the 1H-pyrrole-2-carboxylate ester derivative known as ryanodine, which is a potent… Expand
  • figure 1
Highly Cited
2013
Highly Cited
2013
Anthranilic and phthalic diamides exemplified by chlorantraniliprole (Chlo) or cyantraniliprole (Cyan) and flubendiamide (Flu… Expand
  • figure 1
  • figure 3
  • figure 2
  • figure 4
  • figure 6
2000
2000
In an earlier investigation, we demonstrated that the likelihood of interaction of a positively charged ryanoid, 21-amino-9… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 5
  • figure 4
1999
1999
In this work, we have studied the antifeedant and insecticidal effects of several natural ryanoid diterpenes. These compounds can… Expand
Highly Cited
1996
Highly Cited
1996
We have examined the effects of a number of derivatives of ryanodine on K+ conduction in the Ca2+ release channel purified from… Expand
Highly Cited
1987
Highly Cited
1987
The topography and toxicological relevance of the Ca2+-ryanodine receptor complex are evaluated with ryanodine and two natural… Expand
Highly Cited
1979
Highly Cited
1979
-Pyrrolecarboxylate ester the active insecticidal component in the roots and stems of Ryana speciosa; binds nearly irreversibly… Expand
  • figure 1