Literature DB >> 27433555

Clerodane diterpenes: sources, structures, and biological activities.

Rongtao Li1, Susan L Morris-Natschke, Kuo-Hsiung Lee.   

Abstract

Covering: 1990 to 2015The clerodane diterpenoids are a widespread class of secondary metabolites and have been found in several hundreds of plant species from various families and in organisms from other taxonomic groups. These substances have attracted interest in recent years due to their notable biological activities, particularly insect antifeedant properties. In addition, the major active clerodanes of Salvia divinorum can be used as novel opioid receptor probes, allowing greater insight into opioid receptor-mediated phenomena, as well as opening additional areas for chemical investigation. This article provides extensive coverage of naturally occurring clerodane diterpenes discovered from 1990 until 2015, and follows up on the 1992 review by Merritt and Ley in this same journal. The distribution, chemotaxonomic significance, chemical structures, and biological activities of clerodane diterpenes are summarized. In the cases where sufficient information is available, structure activity relationship (SAR) correlations and mode of action of active clerodanes have been presented.

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Year:  2016        PMID: 27433555      PMCID: PMC5154363          DOI: 10.1039/c5np00137d

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  269 in total

1.  Responses of Spodoptera littoralis larvae to Tunisian plant extracts and to neo-clerodane diterpenoids isolated from Ajuga pseudoiva leaves.

Authors:  H Ben Jannet ; F Harzallah-Skhiri; Z Mighri; M S Simmonds; W M Blaney
Journal:  Fitoterapia       Date:  2000-04       Impact factor: 2.882

2.  Inhibition of human sPLA2 and 5-lipoxygenase activities by two neo-clerodane diterpenoids.

Authors:  R Benrezzouk; M C Terencio; M L Ferrándiz; A San Feliciano; M Gordaliza; J M Miguel del Corral; M L de la Puente; M J Alcaraz
Journal:  Life Sci       Date:  1999       Impact factor: 5.037

3.  Polystachynes A-E, five cis-neo-clerodane diterpenoids from Salvia polystachya.

Authors:  E Maldonado; A Ortega
Journal:  Phytochemistry       Date:  2000-01       Impact factor: 4.072

4.  Anti-tumour activity of two 19-nor-clerodane diterpenes, trans-dehydrocrotonin and trans-crotonin, from Croton cajucara.

Authors:  N F Grynberg; A Echevarria; J E Lima; S S Pamplona; A C Pinto; M A Maciel
Journal:  Planta Med       Date:  1999-12       Impact factor: 3.352

5.  Antioestrogenic effect of trans-dehydrocrotonin, a nor-clerodane diterpene from Croton cajucara Benth. in rats.

Authors:  A M Luna Costa; J C Silva; A R Campos; V S Rao; M A Maciel; A C Pinto
Journal:  Phytother Res       Date:  1999-12       Impact factor: 5.878

6.  Structure-antifeedant activity relationship of clerodane diterpenoids. Comparative study with withanolides and azadirachtin.

Authors:  R D Enriz; H A Baldoni; M A Zamora; E A Jáuregui; M E Sosa; C E Tonn; J M Luco; M Gordaliza
Journal:  J Agric Food Chem       Date:  2000-04       Impact factor: 5.279

7.  Antiulcerogenic mechanisms of dehydrocrotonin, a diterpene lactone obtained from Croton cajucara.

Authors:  C A Hiruma-Lima; R C Spadari-Bratfisch; D M Grassi-Kassisse; A R Brito
Journal:  Planta Med       Date:  1999-05       Impact factor: 3.352

8.  Novel cytotoxic diterpenes from Casearia arborea.

Authors:  J A Beutler; K L McCall; K Herbert; D L Herald; G R Pettit; T Johnson; R H Shoemaker; M R Boyd
Journal:  J Nat Prod       Date:  2000-05       Impact factor: 4.050

9.  Ethnopharmacology, phytochemistry and pharmacology: a successful combination in the study of Croton cajucara.

Authors:  M A Maciel; A C Pinto; A C Arruda; S G Pamplona; F A Vanderlinde; A J Lapa; A Echevarria; N F Grynberg; I M Côlus; R A Farias; A M Luna Costa; V S Rao
Journal:  J Ethnopharmacol       Date:  2000-04       Impact factor: 4.360

10.  Nasimaluns A and B: neo-clerodane diterpenoids from barringtonia racemosa.

Authors:  C M Hasan; S Khan; A Jabbar; M A Rashid
Journal:  J Nat Prod       Date:  2000-03       Impact factor: 4.050

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  29 in total

1.  Semisynthesis and Kappa-Opioid Receptor Activity of Derivatives of Columbin, a Furanolactone Diterpene.

Authors:  Anil Yilmaz; Rachel Saylor Crowley; Alexander M Sherwood; Thomas E Prisinzano
Journal:  J Nat Prod       Date:  2017-07-18       Impact factor: 4.050

2.  Anacolosins A-F and Corymbulosins X and Y, Clerodane Diterpenes from Anacolosa clarkii Exhibiting Cytotoxicity toward Pediatric Cancer Cell Lines.

Authors:  Shengxin Cai; April L Risinger; Cora L Petersen; Tanja Grkovic; Barry R O'Keefe; Susan L Mooberry; Robert H Cichewicz
Journal:  J Nat Prod       Date:  2019-03-04       Impact factor: 4.050

3.  Corymbulosins I-W, Cytotoxic Clerodane Diterpenes from the Bark of Laetia corymbulosa.

Authors:  Simayijiang Aimaiti; Airi Suzuki; Yohei Saito; Shuichi Fukuyoshi; Masuo Goto; Katsunori Miyake; David J Newman; Barry R O'Keefe; Kuo-Hsiung Lee; Kyoko Nakagawa-Goto
Journal:  J Org Chem       Date:  2018-01-10       Impact factor: 4.354

4.  Corymbulosins D-H, 2-Hydroxy- and 2-Oxo-clerodane Diterpenes from the Bark of Laetia corymbulosa.

Authors:  Airi Suzuki; Yohei Saito; Shuichi Fukuyoshi; Masuo Goto; Katsunori Miyake; David J Newman; Barry R O'Keefe; Kuo-Hsiung Lee; Kyoko Nakagawa-Goto
Journal:  J Nat Prod       Date:  2017-03-14       Impact factor: 4.050

5.  Clerodane furanoditerpenoids from the stems of Tinospora sinensis.

Authors:  Jun-Sheng Zhang; De-Feng Xu; Yin-Yin Wang; Ren-Fen Ma; Hua Zhang
Journal:  Arch Pharm Res       Date:  2022-04-27       Impact factor: 4.946

Review 6.  New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017-2022.

Authors:  Cristina Forzato; Patrizia Nitti
Journal:  Plants (Basel)       Date:  2022-08-29

7.  Functional Diversity of Diterpene Synthases in the Biofuel Crop Switchgrass.

Authors:  Kyle A Pelot; Ruibing Chen; David M Hagelthorn; Cari A Young; J Bennett Addison; Andrew Muchlinski; Dorothea Tholl; Philipp Zerbe
Journal:  Plant Physiol       Date:  2018-07-15       Impact factor: 8.340

8.  A novel, semi-synthetic diterpenoid 16(R and S)-phenylamino-cleroda-3,13(14), Z-dien-15,16 olide (PGEA-AN) inhibits the growth and cell survival of human neuroblastoma cell line SH-SY5Y by modulating P53 pathway.

Authors:  Syed Saad Hussain; Kinza Rafi; Shaheen Faizi; Zaid Abdul Razzak; Shabana U Simjee
Journal:  Mol Cell Biochem       Date:  2018-04-11       Impact factor: 3.396

Review 9.  Building trans-bicyclo[4.4.0]decanes/decenes in complex multifunctional frameworks: the case for antibiotic development.

Authors:  Wanli Zhang; Anna R Kaplan; Emma K Davison; Jared L Freeman; Margaret A Brimble; William M Wuest
Journal:  Nat Prod Rep       Date:  2021-05-26       Impact factor: 13.423

10.  Chemical Fractionation Joint to In-Mixture NMR Analysis for Avoiding the Hepatotoxicity of Teucrium chamaedrys L. subsp. chamaedrys.

Authors:  Simona Piccolella; Monica Scognamiglio; Brigida D'Abrosca; Assunta Esposito; Antonio Fiorentino; Severina Pacifico
Journal:  Biomolecules       Date:  2021-05-05
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