scholarly journals Non-alkaloidal constituents from the genus Aconitum: a review

RSC Advances ◽  
2019 ◽  
Vol 9 (18) ◽  
pp. 10184-10194 ◽  
Author(s):  
Tianpeng Yin ◽  
Hao Zhou ◽  
Le Cai ◽  
Zhongtao Ding
Keyword(s):  
Alkaloidal Constituents ◽  
Novel Structures

Multiple non-alkaloidal constituents from Aconitum showed great research significance for their novel structures, broad bioactivities and chemotaxonomical significance.

Indole alkaloids from plants: Novel structures, bioactivities and preclinical investigations

Planta Medica ◽  
2015 ◽  
Vol 81 (05) ◽  
Author(s):  
XH Cai ◽  
T Feng ◽  
XN Li ◽  
YP Liu ◽  
JH Shang ◽  
...  
Keyword(s):  
Indole Alkaloids ◽  
Novel Structures

Flavonoids and other Non-Alkaloidal Constituents of Genus Erythrina: A Detailed Account of Phytochemical Review

2019 ◽  
Vol 23 ◽  
Author(s):  
Ninh The Son ◽  
Abdelsamed I. Elshamymistry
Keyword(s):  
Secondary Metabolites ◽  
Web Of Science ◽  
Herbal Medicines ◽  
Original Research ◽  
Chemical Structures ◽  
Fatty Acid Derivatives ◽  
Material Sources ◽  
Anti Cancer ◽  
Alkaloidal Constituents ◽  
The Web

: Genus Erythrina belongs to family Fabaceae, which widely distributed in tropical and subtropical areas, and has been applied in both traditional herbal medicines, and pharmacological uses. Original research articles and publications on overview of alkaloids related to this genus are available, but a supportive systematic review account highlighted phytochemical aspects of other types of secondary metabolites is now insufficient. Utilizing data information from SCI-Finder, Google Scholar, the Web of Science, Scopus, Science Direct, PubMed, Chemical Abstracts, ACS journals, Springer, Taylor Francis, Bentham Science and IOP Science, the reliable material sources of this systematic manuscript paper were obtained from the literature published from 1980s to now. A vast amount of data showed that the non-alkaloidal secondary metabolites obtained from genus Erythrina with various classes of chemical structures. Herein, approximately five hundred constituents were isolated comprising of flavonoids, terpenoids, saponins, phytosterols, phenols, arylbenzofurans, coumarins, alcohols, ceramides, mono-sugars and fatty acid derivatives. It resembles the previously phytochemical reports on the plants of differential genus of family Fabaceae, flavonoids reached to the high amount in plants of genus Erythrina. Numerous biological researches such as anti-microbacteria, anti-cancer, anti-virus using isolated compounds from Erythrina species suggested that secondary metabolites of Erythrina plants are now becoming promising agents for drug developments.

Bioprospecting Cryptogams as Potential Source of Unique Biodynamic Phytochemicals with Diverse Pharmaceutical Applications

2016 ◽  
Vol 1 (1) ◽  
Author(s):  
Brahma N. Singh ◽  
Garima Pandey ◽  
Prateeksha ◽  
J. Kumar
Keyword(s):  
Secondary Metabolites ◽  
Higher Plants ◽  
New Drugs ◽  
Terrestrial Plants ◽  
Pharmacological Activities ◽  
Therapeutic Drugs ◽  
Potential Source ◽  
Therapeutic Value ◽  
Wide Range ◽  
Novel Structures

With the advent of green pharmaceuticals, the secondary metabolites derived from plants have provided numerous leads for the development of a wide range of therapeutic drugs; however the discovery of new drugs with novel structures has declined in the past few years. Cryptogams including lichens, bryophytes, and pteridophytes represent a group of small terrestrial plants that remain relatively untouched in the drug discovery process though some have been used as ethnomedicines by various tribes worldwide. Studies of their secondary metabolites are recent but reveal unique secondary metabolites which are not synthesized by higher plants. These compounds can have the potential to develop more potential herbal drugs for prevention and treatment of diseases The present article . deals with the secondary metabolites and pharmacological activities of cryptogams with an objective to bring them forth as potential source of biodynamic compounds of therapeutic value.

Submandibular glands: novel structures participating in thermoregulatory responses

1997 ◽  
Vol 75 (5) ◽  
pp. 407-413 ◽  
Author(s):  
R D Mathison ◽  
T Malkinson ◽  
K E Cooper ◽  
J S Davison
Keyword(s):  
Submandibular Glands ◽  
Thermoregulatory Responses ◽  
Novel Structures

Designing novel structures with hierarchically synchronized deformations

2018 ◽  
Vol 19 ◽  
pp. 1-6 ◽  
Author(s):  
Dingjie Lu ◽  
Yang Fan Li ◽  
Hamed Seifi ◽  
Shiwei Zhou ◽  
Zi-Long Zhao ◽  
...  
Keyword(s):  
Novel Structures

Design of Static Test Model for Three-Tower Cable-Stayed Self-Anchored Suspension Composed Bridge

2011 ◽  
Vol 243-249 ◽  
pp. 1528-1535
Author(s):  
Yu Zhao ◽  
Yong Jun Zhou ◽  
Jing Sun ◽  
Jin Tao Tang ◽  
Xu Li
Keyword(s):  
Complex System ◽  
Finite Element ◽  
Element Model ◽  
Test Model ◽  
Test Results ◽  
Static Test ◽  
Whole Process ◽  
Aesthetic Appearance ◽  
Load Carrying ◽  
Novel Structures

Cable-stayed self-anchored suspension composed bridges have novel structures and aesthetic appearance with complex system and difficulty for design and construction. In order to acquire a better knowledge of the load-carrying capability of this type of bridges, based on a real bridge and the theory of abnormal similarity, a full-bridge scaled down(1:20) test model was built to simulate the whole process of construction. The test results were preferably fit the theoretical calculation value. It can be seen that the design of the bridge was reasonable, and the accuracy of the calculation of finite element model was verified at the same time. The test and the related results can be used as the reference for the test and design of the similar bridges.

Novel structures in galactoglucomannans of the lichens Cladonia substellata and Cladonia ibitipocae: significance as chemotypes

1999 ◽  
Vol 51 (3) ◽  
pp. 395-402 ◽  
Author(s):  
Sandra M Woranovicz ◽  
B.Mario Pinto ◽  
Philip A.J Gorin ◽  
Marcello Iacomini
Keyword(s):  
Novel Structures

Complexes with phosphinomethane and phosphinomethanide ligands. 17. Lithium phosphinomethanides: two novel structures

1990 ◽  
Vol 9 (1) ◽  
pp. 190-194 ◽  
Author(s):  
Hans H. Karsch ◽  
Karin Zellner ◽  
Patrizia Mikulcik ◽  
Joachim Lachmann ◽  
Gerhard Mueller
Keyword(s):  
Novel Structures
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