Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR

[1]  H. Lv,et al.  Rhodomollins A and B, two Diterpenoids with an Unprecedented Backbone from the Fruits of Rhododendron molle , 2016, Scientific Reports.

[2]  Jian-Dong Jiang,et al.  Antiviral Spirotriscoumarins A and B: Two Pairs of Oligomeric Coumarin Enantiomers with a Spirodienone-Sesquiterpene Skeleton from Toddalia asiatica. , 2016, Organic letters.

[3]  Shuang-Gang Ma,et al.  Analgesic Diterpenoids from the Twigs of Pieris formosa. , 2016 .

[4]  H. Lv,et al.  Antinociceptive Grayanoids from the Roots of Rhododendron molle. , 2015, Journal of natural products.

[5]  C. Chou,et al.  Structure Elucidation of Procyanidins Isolated from Rhododendron formosanum and Their Anti-Oxidative and Anti-Bacterial Activities , 2015, Molecules.

[6]  Min‐Su Han,et al.  Anti-Inflammatory Effects of Hyperoside in Human Endothelial Cells and in Mice , 2015, Inflammation.

[7]  S. Habtemariam,et al.  Inhibitory effects of lupene-derived pentacyclic triterpenoids from Bursera simaruba on HSV-1 and HSV-2 in vitro replication , 2015, Natural product research.

[8]  Shuang-Gang Ma,et al.  Mollanol A, a diterpenoid with a new C-nor-D-homograyanane skeleton from the fruits of Rhododendron molle. , 2014, Organic letters.

[9]  Qing-lan Guo,et al.  A minor diterpenoid with a new 6/5/7/3 fused-ring skeleton from Euphorbia micractina. , 2014, Organic letters.

[10]  Q. Hou,et al.  Five new compounds from Rhododendron mariae Hance , 2014, Journal of Asian natural products research.

[11]  W. Zhou,et al.  Phytochemical Studies of Korean Endangered Plants: A New Flavone from Rhododendron brachycarpum G. Don. , 2013 .

[12]  R. Ventura-Martínez,et al.  Ursolic acid from Agastache mexicana aerial parts produces antinociceptive activity involving TRPV1 receptors, cGMP and a serotonergic synergism , 2013, Pharmacology Biochemistry and Behavior.

[13]  Wei Zhou,et al.  Phytochemical Studies of Korean Endangered Plants: A New Flavone from Rhododendron brachycarpum G.Don , 2013 .

[14]  Jian-Dong Jiang,et al.  Mollolide A, a diterpenoid with a new 1,10:2,3-disecograyanane skeleton from the roots of Rhododendron molle. , 2013, Organic letters.

[15]  Sheng Lin,et al.  Enantiomers of an indole alkaloid containing unusual dihydrothiopyran and 1,2,4-thiadiazole rings from the root of Isatis indigotica. , 2012, Organic Letters.

[16]  Huiru Tang,et al.  Identification of three novel polyphenolic compounds, origanine A-C, with unique skeleton from Origanum vulgare L. using the hyphenated LC-DAD-SPE-NMR/MS methods. , 2012, Journal of agricultural and food chemistry.

[17]  Jian-Dong Jiang,et al.  Synthesis and Biological Evaluation of Heat-Shock Protein 90 Inhibitors: Geldanamycin Derivatives with Broad Antiviral Activities , 2010, Antiviral chemistry & chemotherapy.

[18]  S. Moco,et al.  LC-MS-SPE-NMR for the isolation and characterization of neo-clerodane diterpenoids from Teucrium luteum subsp. flavovirens (perpendicular). , 2010, Journal of natural products.

[19]  Rodrigo Duarte Soliani,et al.  Phytochemical Characterization of Rhododendron ferrugineum and In Vitro Assessment of an Aqueous Extract on Cell Toxicity , 2010, Planta medica.

[20]  Y. Liu,et al.  Immunomodulatory effects of proanthocyanidin A-1 derived in vitro from Rhododendron spiciferum. , 2010, Fitoterapia.

[21]  K. Kashima,et al.  Ovafolinins A-E, five new lignans from Lyonia ovalifolia. , 2010, Chemical & pharmaceutical bulletin.

[22]  G. Qin,et al.  Phenolic glucosides from the leaves of Pieris japonica. , 2008, Yao xue xue bao = Acta pharmaceutica Sinica.

[23]  Helen Skaltsa,et al.  Minor sesquiterpene lactones from Centaurea pullata and their antimicrobial activity. , 2007, Journal of natural products.

[24]  M. Alcaraz,et al.  Activity of lupane triterpenoids from Maytenus species as inhibitors of nitric oxide and prostaglandin E2. , 2006, Bioorganic & medicinal chemistry.

[25]  U. Farooq,et al.  Tyrosinase Inhibitors from Rhododendron collettianum and Their Structure—Activity Relationship (SAR) Studies. , 2005 .

[26]  S. Sacks,et al.  The synergistic effects of betulin with acyclovir against herpes simplex viruses. , 2004, Antiviral research.

[27]  P. McPhie,et al.  Circular Dichroism: Principles and Applications, Second ed. Edited by Nina Berova, Koji Nakanishi, and Robert W. Woody , 2001 .

[28]  G. Qin,et al.  Constituents from the leaves of Rhododendron latoucheae. , 2001, Fitoterapia.

[29]  Y. Fukuyama,et al.  Triterpene and flavanone glycoside from Rhododendron simsii. , 2001, Phytochemistry.

[30]  K. Lee,et al.  Isolation of rhododaurichromanic acid B and the anti-HIV principles rhododaurichromanic acid A and rhododaurichromenic acid from Rhododendron dauricum , 2001 .

[31]  N. Berova,et al.  Circular Dichroism: Principles and Applications , 1994 .

[32]  E. Engvall,et al.  Enzyme-linked immunosorbent assay (ELISA). Quantitative assay of immunoglobulin G. , 1971, Immunochemistry.

[33]  L. Rao,et al.  Phytochemicals – A Global Perspective of Their Role in Nutrition and Health 468 Category Subclass Structure Common Flavonoid Food Examples Phenolic acids Hydroxycinnamic acids Caffeic acid coffee beans , 2012 .

[34]  J. Gawroński.  Circular dichroism and stereochemistry of chiral conjugated cyclohexenones , 1982 .

[35]  A. Scott,et al.  Stereochemistry of olefins—IX : Correlation of Mills' and Brewster's rules with the Cotton effects of cyclic olefins☆ , 1971 .

[36]  A. Scott,et al.  A symmetry rule for chiral olefins , 1969 .

[37]  G. Snatzke,et al.  Circular Dichroism and Optical Rotatory Dispersion — Principles and Application to the Investigation of the Stereochemistry of Natural Products† , 1968 .

[38]  E. Charney,et al.  Optical activity of non-planar conjugated dienes. I. Homoannular cisoid dienes. , 1965, Tetrahedron.

[39]  E. Charney,et al.  Optical activity of non-planar conjugated dienes. II. Transoid dienes. , 1965, Tetrahedron.