Related references
Note: Only part of the references are listed.Betulin and its derivatives as novel compounds with different pharmacological effects
Shayan Amiri et al.
BIOTECHNOLOGY ADVANCES (2020)
Synthesis, structure activity relationship and in vitro anti-influenza virus activity of novel polyphenol-pentacyclic triterpene conjugates
Haiwei Li et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2019)
Triphenylphosphonium Analogues of Betulin and Betulinic Acid with Biological Activity: A Comprehensive Review
Miroslawa Grymel et al.
JOURNAL OF NATURAL PRODUCTS (2019)
2-Deoxyglycoside Conjugates of Lupane Triterpenoids with High Cytotoxic Activity-Synthesis, Activity, and Pharmacokinetic Profile
Pavla Perlikova et al.
BIOCONJUGATE CHEMISTRY (2019)
Cyclodextrins: structure, physicochemical properties and pharmaceutical applications
Phatsawee Jansook et al.
INTERNATIONAL JOURNAL OF PHARMACEUTICS (2018)
Amino cyclodextrin per-O-methylation: Synthesis of 3-monoamino-permethylated derivatives
Golfo G. Kordopati et al.
TETRAHEDRON LETTERS (2018)
Cyclodextrin complexes: Perspective from drug delivery and formulation
Shery Jacob et al.
DRUG DEVELOPMENT RESEARCH (2018)
Oleanane-, ursane-, and quinone methide friedelane-type triterpenoid derivatives: Recent advances in cancer treatment
Jorge A. R. Salvador et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2017)
Design, Synthesis, and Cancer Cell Growth Inhibitory Activity of Triphenylphosphonium Derivatives of the Triterpenoid Betulin
Olga V. Tsepaeva et al.
JOURNAL OF NATURAL PRODUCTS (2017)
Release of Cytochrome C from Bax Pores at the Mitochondrial Membrane
Mingzhen Zhang et al.
SCIENTIFIC REPORTS (2017)
Peptide-Appended Permethylated β-Cyclodextrins with Hydrophilic and Hydrophobic Spacers
Abbas H. K. Al Temimi et al.
BIOCONJUGATE CHEMISTRY (2017)
Activation of apoptosis signalling pathways by reactive oxygen species
Maureen Redza-Dutordoir et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2016)
In vitro anticancer activity of Betulinic acid and derivatives thereof on equine melanoma cell lines from grey horses and invivo safety assessment of the compound NVX-207 in two horses
G. Liebscher et al.
CHEMICO-BIOLOGICAL INTERACTIONS (2016)
Betulinic Acid and its Derivatives as Potential Antitumor Agents
Dong-Mei Zhang et al.
MEDICINAL RESEARCH REVIEWS (2015)
Conjugates of methylated cyclodextrin derivatives and hydroxyethyl starch (HES): Synthesis, cytotoxicity and inclusion of anaesthetic actives
Lisa Markenstein et al.
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY (2014)
Oleanolic acid and its synthetic derivatives for the prevention and therapy of cancer: Preclinical and clinical evidence
Muthu K. Shanmugam et al.
CANCER LETTERS (2014)
Synthesis and Anti- HCV Entry Activity Studies of bCyclodextrin- Pentacyclic Triterpene Conjugates
Sulong Xiao et al.
CHEMMEDCHEM (2014)
New Improved Drug Delivery Technologies for Pentacyclic Triterpenes: A Review
Codruta Soica et al.
PROTEIN AND PEPTIDE LETTERS (2014)
Supramolecular Iron Porphyrin/Cyclodextrin Dimer Complex that Mimics the Functions of Hemoglobin and Methemoglobin
Kenji Watanabe et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2013)
Potential use of Folate-appended Methyl-β-Cyclodextrin as an Anticancer Agent
Risako Onodera et al.
SCIENTIFIC REPORTS (2013)
In vitro anticancer studies of α- and β-D-glucopyranose betulin anomers
Harish Kommera et al.
CHEMICO-BIOLOGICAL INTERACTIONS (2010)
Characterization of NVX-207, a novel betulinic acid-derived anti-cancer compound
M. Willmann et al.
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION (2009)
The unambiguous assignment of NMR spectra of per-O-methylated 6-mono and 6,6-diamino-β-cyclodextrins
Eduardo Diaz T. et al.
CANADIAN JOURNAL OF CHEMISTRY (2008)
Solubility studies of oleanolic acid and betulinic acid in aqueous solutions and plant extracts of Viscum album L.
Sebastian Jaeger et al.
PLANTA MEDICA (2007)
Boc-lysinated-betulonic acid: A potent, anti-prostate cancer agent
Brij B. Saxena et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2006)
Pharmacological activities of natural triterpenoids and their therapeutic implications
Petr Dzubak et al.
NATURAL PRODUCT REPORTS (2006)
Cyclodextrin-based pharmaceutics: Past, present and future
ME Davis et al.
NATURE REVIEWS DRUG DISCOVERY (2004)
New large-scale preparations of versatile 6-O-monotosyl and 6-monohydroxy permethylated α-, β-, and γ-cyclodextrins
T Kaneda et al.
CHEMISTRY LETTERS (2002)
Synthesis of the three isomeric mono-2-, 3-, or 6-hydroxy permethylated β-cyclodextrins and unambiguous high field NMR characterisation
H Cousin et al.
TETRAHEDRON-ASYMMETRY (2001)