Diterpenoids: Natural Distribution, Semisynthesis at Room Temperature and Pharmacological Aspects‐A Decade Update
出版年份 2020 全文链接
标题
Diterpenoids: Natural Distribution, Semisynthesis at Room Temperature and Pharmacological Aspects‐A Decade Update
作者
关键词
-
出版物
ChemistrySelect
Volume -, Issue -, Pages -
出版商
Wiley
发表日期
2020-10-12
DOI
10.1002/slct.202002836
参考文献
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注意：仅列出部分参考文献，下载原文获取全部文献信息。- Semisynthesis of epoxy-pimarane diterpenoids from kirenol and their FXa inhibition activities
- (2019) Jianbin Wang et al. BIOORGANIC & MEDICINAL CHEMISTRY
- Semi-synthesis and structural elucidation of brevicanines A–D, four new C19-diterpenoid alkaloids with rotameric phenomenon from Aconitum brevicalcaratum
- (2019) Zhong-Sheng Wang et al. FITOTERAPIA
- A Review on Daphnane-Type Diterpenoids and Their Bioactive Studies
- (2019) Yue-Xian Jin et al. MOLECULES
- Semisynthesis of the Neuroprotective Metabolite, Serofendic Acid
- (2019) Szu-Yi Hsu et al. ACS Synthetic Biology
- Chemoenzymatic Semisynthesis of Proteins
- (2019) Robert E. Thompson et al. CHEMICAL REVIEWS
- Inhibition of squalene synthase of rat liver by abietane diterpenes derivatives
- (2019) Mariana Macías-Alonso et al. NATURAL PRODUCT RESEARCH
- Semisynthesis of ent -norstrobane diterpenoids as potential inhibitor for factor Xa
- (2018) Jianbin Wang et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Annonalide and derivatives: Semisynthesis, cytotoxic activities and studies on interaction of annonalide with DNA
- (2018) Ricardo A. Marques et al. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY
- Halimane diterpenoids: sources, structures, nomenclature and biological activities
- (2018) Alejandro M. Roncero et al. NATURAL PRODUCT REPORTS
- Semisynthesis and Kappa-Opioid Receptor Activity of Derivatives of Columbin, a Furanolactone Diterpene
- (2017) Anil Yilmaz et al. JOURNAL OF NATURAL PRODUCTS
- The modification of natural products for medical use
- (2017) Zongru Guo Acta Pharmaceutica Sinica B
- ent-Strobane and ent-Pimarane Diterpenoids from Siegesbeckia pubescens
- (2016) Jianbin Wang et al. JOURNAL OF NATURAL PRODUCTS
- Natural Products as Sources of New Drugs from 1981 to 2014
- (2016) David J. Newman et al. JOURNAL OF NATURAL PRODUCTS
- The use of isolated natural products as scaffolds for the generation of chemically diverse screening libraries for drug discovery
- (2016) Emma C. Barnes et al. NATURAL PRODUCT REPORTS
- Clerodane diterpenes: sources, structures, and biological activities
- (2016) Rongtao Li et al. NATURAL PRODUCT REPORTS
- Tigliane Diterpenoids from the Euphorbiaceae and Thymelaeaceae Families
- (2015) Hong-Bing Wang et al. CHEMICAL REVIEWS
- Green Solvents in Carbohydrate Chemistry: From Raw Materials to Fine Chemicals
- (2015) Angeles Farrán et al. CHEMICAL REVIEWS
- Semisynthesis and in vitro cytotoxic evaluation of new analogues of 1-O-acetylbritannilactone, a sesquiterpene from Inula britannica
- (2014) Shuai Dong et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Isolation of a novel paxilline analog pyrapaxilline from fungus that inhibits LPS-induced NO production
- (2014) Chino Matsui et al. JOURNAL OF ANTIBIOTICS
- Semisynthesis of the Antiviral Abietane Diterpenoid Jiadifenoic Acid C from Callitrisic Acid (4-Epidehydroabietic Acid) Isolated from Sandarac Resin
- (2014) Miguel A. González et al. JOURNAL OF NATURAL PRODUCTS
- Further Mulinane and Azorellane Diterpenoids Isolated from Mulinum crassifolium and Azorella compacta
- (2014) Jorge Bórquez et al. MOLECULES
- Semisynthesis of Macrocarpal C and Analogues by Selective Dehydration of Macrocarpal A or B
- (2013) Julien Alliot et al. JOURNAL OF NATURAL PRODUCTS
- Diterpenoids of terrestrial origin
- (2013) James R. Hanson NATURAL PRODUCT REPORTS
- Regio- and stereoselective synthesis of (+)-6-ketoeuryfuran, (+)-6-ketowinterin, and (−)-7-ketoeuryfuran from accessible labdane diterpenoids (+)-larixol and (−)-sclareol
- (2012) Pavel F. Vlad et al. TETRAHEDRON
- A new labdane diterpene from Rauvolfia tetraphylla Linn. (Apocynaceae)
- (2012) Goutam Brahmachari et al. JOURNAL OF CHEMICAL RESEARCH
- Design of semisynthetic analogues and 3D-QSAR study of eunicellin-based diterpenoids as prostate cancer migration and invasion inhibitors
- (2011) Hossam M. Hassan et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Topical anti-inflammatory and analgesic activity of kirenol isolated from Siegesbeckia orientalis
- (2011) Jian-ping Wang et al. JOURNAL OF ETHNOPHARMACOLOGY
- Design and synthesis of de novo cytotoxic alkaloids by mimicking the bioactive conformation of paclitaxel
- (2010) Liang Sun et al. BIOORGANIC & MEDICINAL CHEMISTRY
- A bioactive labdane diterpenoid from Curcuma amada and its semisynthetic analogues as antitubercular agents
- (2010) Sailendra Singh et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Pachycladins A−E, Prostate Cancer Invasion and Migration Inhibitory Eunicellin-Based Diterpenoids from the Red Sea Soft CoralCladiella pachyclados
- (2010) Hossam M. Hassan et al. JOURNAL OF NATURAL PRODUCTS
- Jatropha Diterpenes: a Review
- (2010) Rakshit K. Devappa et al. JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY
- Natural Product Synthesis Using Multicomponent Reaction Strategies
- (2009) Barry B. Touré et al. CHEMICAL REVIEWS
- Antituberculosis activity of natural and semisynthetic azorellane and mulinane diterpenoids
- (2009) Gloria María Molina-Salinas et al. FITOTERAPIA
- Semisynthesis and Biological Evaluation of Abietane-Type Diterpenes. Revision of the Structure of Rosmaquinone
- (2009) Joaquín G. Marrero et al. JOURNAL OF NATURAL PRODUCTS
- Diterpenoids
- (2009) James R. Hanson NATURAL PRODUCT REPORTS
- The 24 Principles of Green Engineering and Green Chemistry: “IMPROVEMENTS PRODUCTIVELY”
- (2008) Samantha Y. Tang et al. GREEN CHEMISTRY
- Synthesis of Drim-7,9(11)-diene and Its Hydroxylated Derivatives
- (2008) Pavel F. Vlad et al. SYNTHETIC COMMUNICATIONS
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