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Journal articles on the topic 'Phytochemistry; Biology'

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Published: 7 July 2024

Last updated: 7 July 2024

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1

Amadi, Sarah Wambui, Yan Zhang, and Guanzhong Wu. "Research progress in phytochemistry and biology ofAframomumspecies." Pharmaceutical Biology 54, no. 11 (May 9, 2016): 2761–70. http://dx.doi.org/10.3109/13880209.2016.1173068.

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2

Hao, Da-Cheng, Xiaojie Gu, and Peigen Xiao. "Anemone medicinal plants: ethnopharmacology, phytochemistry and biology." Acta Pharmaceutica Sinica B 7, no. 2 (March 2017): 146–58. http://dx.doi.org/10.1016/j.apsb.2016.12.001.

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3

Wang, Hanqing, Jiaoning Li, Weiwei Tao, Xia Zhang, Xiaojuan Gao, Jingjiao Yong, Jianjun Zhao, Liming Zhang, Yongzhou Li, and Jin-ao Duan. "Lycium ruthenicum studies: Molecular biology, Phytochemistry and pharmacology." Food Chemistry 240 (February 2018): 759–66. http://dx.doi.org/10.1016/j.foodchem.2017.08.026.

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4

Bolwell, G. Paul, Norman G. Lewis, and Dieter Strack. "Global phytochemistry." Phytochemistry 55, no. 2 (September 2000): xi. http://dx.doi.org/10.1016/s0031-9422(00)00338-1.

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5

Lewis, Norman G. "Phytochemistry foreword." Phytochemistry 69, no. 18 (December 2008): 3005. http://dx.doi.org/10.1016/j.phytochem.2008.11.002.

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6

Gutiérrez, Rosa Martha Pérez, and Rosalinda Lule Perez. "Raphanus sativus (Radish): Their Chemistry and Biology." Scientific World JOURNAL 4 (2004): 811–37. http://dx.doi.org/10.1100/tsw.2004.131.

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Leaves and roots ofRaphanus sativushave been used in various parts of the world to treat cancer and as antimicrobial and antiviral agents. The phytochemistry and pharmacology of this radish is reviewed. The structures of the compounds isolated and identified are listed and aspects of their chemistry and pharmacology are discussed. The compounds are grouped according to structural classes.

7

Chambers, Christopher, Katerina Valentova, and Vladimir kren. "“Non-Taxifolin” Derived Flavonolignans: Phytochemistry and Biology." Current Pharmaceutical Design 21, no. 38 (November 12, 2015): 5489–500. http://dx.doi.org/10.2174/1381612821666151002112720.

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8

Harborne, Jeffrey B. "Phytochemistry of medicinal plants." Phytochemistry 43, no. 1 (September 1996): 317–18. http://dx.doi.org/10.1016/0031-9422(96)84068-4.

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9

Özenver, Nadire, Monika Efferth, and Thomas Efferth. "Ethnopharmacology, phytochemistry, chemical ecology and invasion biology of Acanthus mollis L." Journal of Ethnopharmacology 285 (March 2022): 114833. http://dx.doi.org/10.1016/j.jep.2021.114833.

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10

Hao, Dacheng, Xiaojie Gu, Peigen Xiao, Zhanguo Liang, Lijia Xu, and Yong Peng. "Research progress in the phytochemistry and biology of Ilex pharmaceutical resources." Acta Pharmaceutica Sinica B 3, no. 1 (February 2013): 8–19. http://dx.doi.org/10.1016/j.apsb.2012.12.008.

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11

Naqvi, Syed Farhad Hussain, and Muhammad Husnain. "Betalains: Potential Drugs with Versatile Phytochemistry." Critical Reviews in Eukaryotic Gene Expression 30, no. 2 (2020): 169–89. http://dx.doi.org/10.1615/critreveukaryotgeneexpr.2020030231.

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12

Duan, Zhi-Kang, Zhao-Jun Zhang, Shu-Hui Dong, Yu-Xi Wang, Shao-Jiang Song, and Xiao-Xiao Huang. "Quassinoids: Phytochemistry and antitumor prospect." Phytochemistry 187 (July 2021): 112769. http://dx.doi.org/10.1016/j.phytochem.2021.112769.

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13

Saleh, Nabiel A. M. "Global phytochemistry: the Egyptian experience." Phytochemistry 63, no. 3 (June 2003): 239–41. http://dx.doi.org/10.1016/s0031-9422(03)00163-8.

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14

Asakawa, Yoshinori. "Global phytochemistry: research in Japan." Phytochemistry 64, no. 5 (November 2003): 909–12. http://dx.doi.org/10.1016/s0031-9422(03)00384-4.

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15

Parmar, Virinder S., Subhash C. Jain, Kirpal S. Bisht, Rajni Jain, Poonam Taneja, Amitabh Jha, Om D. Tyagi, et al. "Phytochemistry of the genus Piper." Phytochemistry 46, no. 4 (October 1997): 597–673. http://dx.doi.org/10.1016/s0031-9422(97)00328-2.

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16

Coşkun, Maksut, and A. Mine Gençler Özkan. "Global phytochemistry: The Turkish frame." Phytochemistry 66, no. 9 (May 2005): 956–60. http://dx.doi.org/10.1016/j.phytochem.2005.03.012.

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17

(Klaus) Fischer, N. H. "Klaus Fischer (PSNA Phytochemistry Pioneer)☆." Phytochemistry 68, no. 14 (July 2007): 1838–41. http://dx.doi.org/10.1016/j.phytochem.2007.05.013.

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18

Petersen, Maike. "Current status of metabolic phytochemistry." Phytochemistry 68, no. 22-24 (November 2007): 2847–60. http://dx.doi.org/10.1016/j.phytochem.2007.07.029.

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19

Colombo, Paola S., Guido Flamini, Graziella Rodondi, Claudia Giuliani, Laura Santagostini, and Gelsomina Fico. "Phytochemistry of European Primula species." Phytochemistry 143 (November 2017): 132–44. http://dx.doi.org/10.1016/j.phytochem.2017.07.005.

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20

Ghisalberti, Emilio L. "The phytochemistry of the myoporaceae." Phytochemistry 35, no. 1 (December 1993): 7–33. http://dx.doi.org/10.1016/s0031-9422(00)90503-x.

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21

Hashidoko, Yasuyuki. "The phytochemistry of Rosa rugosa." Phytochemistry 43, no. 3 (October 1996): 535–49. http://dx.doi.org/10.1016/0031-9422(96)00287-7.

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22

Kumar, KN Sunil. "Opportunities for allied health science subjects in Ayurveda research and development." Journal of Ayurvedic and Herbal Medicine 2, no. 1 (February 25, 2016): 1–2. http://dx.doi.org/10.31254/jahm.2016.2101.

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The science behind Ayurveda has been researched by scholars from Ayurvedic and allied science fraternity. Ayurvedic science is offered as bachelor, master and doctoral degrees from Ayurveda medical colleges and universities. There are courses for allied science subjects such as Pharmacology, Biochemistry, Biotechnology, Molecular biology, Microbiology, Phytochemistry, Pharmacognosy, Botany, Agriculture etc. at all levels of study under every university falling under UGC.

23

Palma-Tenango, Mariana, Rosa E. Sánchez-Fernández, and Marcos Soto-Hernández. "A Systematic Approach to Agastache mexicana Research: Biology, Agronomy, Phytochemistry, and Bioactivity." Molecules 26, no. 12 (June 20, 2021): 3751. http://dx.doi.org/10.3390/molecules26123751.

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Mexico is the center of origin of the species popularly known as toronjil or lemon balm (Agastache mexicana Linton & Epling). Two subspecies have been identified and are commonly called purple or red (Agastache mexicana Linton & Epling subspecies. mexicana) and white (Agastache mexicana subspecies xolocotziana Bye, E.L. Linares & Ramamoorthy). Plants from these subspecies differ in the size and form of inflorescence and leaves. They also possess differences in their chemical compositions, including volatile compounds. Traditional Mexican medicine employs both subspecies. A. mexicana exhibits a broad range of pharmacological properties, such as anti-inflammatory, anxiolytic, and antioxidant. A systematic vision of these plant’s properties is discussed in this review, exposing its significant potential as a source of valuable bioactive compounds. Furthermore, this review provides an understanding of the elements that make up the species’ holistic system to benefit from lemon balm sustainably.

24

Moghadamtousi, Soheil Zorofchian, Muhamad Noor Alfarizal Kamarudin, Chim Kei Chan, Bey Hing Goh, and Habsah Abdul Kadir. "Phytochemistry and Biology of Loranthus parasiticus Merr, a Commonly Used Herbal Medicine." American Journal of Chinese Medicine 42, no. 01 (January 2014): 23–35. http://dx.doi.org/10.1142/s0192415x14500025.

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Loranthus parasiticus Merr (L. parasiticus) is a member of Loranthaceae family and is an important medicinal plant with a long history of Chinese traditional use. L. parasiticus, also known as Sang Ji Sheng (in Chinese), benalu teh (in Malay) and baso-kisei (in Japanese), is a semiparasitic plant, which is mostly distributed in the southern and southwestern regions of China. This review aims to provide a comprehensive overview of the ethnomedicinal use, phytochemistry and pharmacological activity of L. parasiticus and to highlight the needs for further investigation and greater global development of the plant's medicinal properties. To date, pharmacological studies have demonstrated significant biological activities, which support the traditional use of the plant as a neuroprotective, tranquilizing, anticancer, immunomodulatory, antiviral, diuretic and hypotensive agent. In addition, studies have identified antioxidative, antimutagenic, antiviral, antihepatotoxic and antinephrotoxic activity. The key bioactive constituents in L. parasiticus include coriaria lactone comprised of sesquiterpene lactones: coriamyrtin, tutin, corianin, and coriatin. In addition, two proanthocyanidins, namely, AC trimer and (+)-catechin, have been recently discovered as novel to L. parasiticus. L. parasiticus usefulness as a medicinal plant with current widespread traditional use warrants further research, clinical trials and product development to fully exploit its medicinal value.

25

Galindez, Javier de Santos, Lidia Fernández Matellano, and Ana M. Díaz Lanza. "Iridoids from Scrophularia Genus." Zeitschrift für Naturforschung C 56, no. 7-8 (August 1, 2001): 513–20. http://dx.doi.org/10.1515/znc-2001-7-807.

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We report here an updated summary about iridoid composition of a series from the genus Scrophularia which have been investigated until now from a phytochemistry point of view. In addition a list is included about iridoids isolated in our laboratory from different plant parts of Scrophularia scorodonia L.,which are compared with iridoids from some species of the Scrophularia genus. The present study may serve as a current information to researchers working on phytochemistry and pharmacological aspects from the Scrophularia genus and possibly to serve as a new starting point for future investigations

26

Philbin, Casey S., Matthew Paulsen, and Lora A. Richards. "Opposing Effects of Ceanothus velutinus Phytochemistry on Herbivore Communities at Multiple Scales." Metabolites 11, no. 6 (June 7, 2021): 361. http://dx.doi.org/10.3390/metabo11060361.

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Identifying the interactions of functional, biotic, and abiotic factors that define plant–insect communities has long been a goal of community ecologists. Metabolomics approaches facilitate a broader understanding of how phytochemistry mediates the functional interactions among ecological factors. Ceanothus velutinus communities are a relatively unstudied system for investigating chemically mediated interactions. Ceanothus are nitrogen-fixing, fire-adapted plants that establish early post-fire, and produce antimicrobial cyclic peptides, linear peptides, and flavonoids. This study takes a metabolomic approach to understanding how the diversity and variation of C. velutinus phytochemistry influences associated herbivore and parasitoid communities at multiple spatiotemporal scales. Herbivores and foliar samples were collected over three collection times at two sites on the east slope of the Sierra Nevada Mountain range. Foliar tissue was subjected to LC-MS metabolomic analysis, and several novel statistical analyses were applied to summarize, quantify, and annotate variation in the C. velutinus metabolome. We found that phytochemistry played an important role in plant–insect community structure across an elevational gradient. Flavonoids were found to mediate biotic and abiotic influences on herbivores and associated parasitoids, while foliar oligopeptides played a significant positive role in herbivore abundance, even more than abundance of host plants and leaf abundance. The importance of nutritional and defense chemistry in mediating ecological interactions in C. velutinus plant–herbivore communities was established, justifying larger scale studies of this plant system that incorporate other mediators of phytochemistry such as genetic and metageomic contributions.

27

Ferreira, Daneel, Jannie P. J. Marais, and Desmond Slade. "Phytochemistry of the mopane, Colophospermum mopane." Phytochemistry 64, no. 1 (September 2003): 31–51. http://dx.doi.org/10.1016/s0031-9422(03)00152-3.

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28

Larsson, Sonny. "The “new” chemosystematics: Phylogeny and phytochemistry." Phytochemistry 68, no. 22-24 (November 2007): 2904–8. http://dx.doi.org/10.1016/j.phytochem.2007.09.015.

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29

Robins, Richard, G. Paul Bolwell, and Norman G. Lewis. "Phytochemistry and the new technologies: Tackling the critical barriers to advancing systems biology." Phytochemistry 68, no. 16-18 (August 2007): 2134–35. http://dx.doi.org/10.1016/j.phytochem.2007.06.002.

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30

Harneti, Desi, and Unang Supratman. "Phytochemistry and biological activities of Aglaia species." Phytochemistry 181 (January 2021): 112540. http://dx.doi.org/10.1016/j.phytochem.2020.112540.

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31

Brown, Stewart A. "Dr. Stewart A. Brown (PSNA Phytochemistry Pioneer)☆." Phytochemistry 68, no. 14 (July 2007): 1830–33. http://dx.doi.org/10.1016/j.phytochem.2007.05.009.

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32

Macías, Francisco A., Jose L. G. Galindo, and Juan C. G. Galindo. "Evolution and current status of ecological phytochemistry." Phytochemistry 68, no. 22-24 (November 2007): 2917–36. http://dx.doi.org/10.1016/j.phytochem.2007.10.010.

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33

Rizwan, Komal, Ismat Majeed, Muhammad Bilal, Tahir Rasheed, Ahmad Shakeel, and Shahid Iqbal. "Phytochemistry and Diverse Pharmacology of Genus Mimosa: A Review." Biomolecules 12, no. 1 (January 5, 2022): 83. http://dx.doi.org/10.3390/biom12010083.

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The genus Mimosa belongs to the Fabaceae family and comprises almost 400 species of herbs, shrubs and ornamental trees. The genus Mimosa is found all over the tropics and subtropics of Asia, Africa, South America, North America and Australia. Traditionally, this genus has been popular for the treatment of jaundice, diarrhea, fever, toothache, wound healing, asthma, leprosy, vaginal and urinary complaints, skin diseases, piles, gastrointestinal disorders, small pox, hepatitis, tumor, HIV, ulcers and ringworm. The review covered literature available from 1959 to 2020 collected from books, scientific journals and electronic searches, such as Science Direct, Web of Science and Google scholar. Various keywords, such as Mimosa, secondary metabolites, medicines, phytochemicals and pharmacological values, were used for the data search. The Mimosa species are acknowledged to be an essential source of secondary metabolites with a wide-ranging biological functions, and up until now, 145 compounds have been isolated from this genus. Pharmacological studies showed that isolated compounds possess significant potential, such as antiprotozoal, antimicrobial, antiviral, antioxidant, and antiproliferative as well as cytotoxic activities. Alkaloids, chalcones, flavonoids, indoles, terpenes, terpenoids, saponins, steroids, amino acids, glycosides, flavanols, phenols, lignoids, polysaccharides, lignins, salts and fatty esters have been isolated from this genus. This review focused on the medicinal aspects of the Mimosa species and may provide a comprehensive understanding of the prospective of this genus as a foundation of medicine, supplement and nourishment. The plants of this genus could be a potential source of medicines in the near future.

34

Tematio Fouedjou, Romuald, Bienvenu Tsakem, Xavier Siwe-Noundou, Hervet P. Dongmo Fogang, Aphalaine Tiombou Donkia, Beaudelaire Kemvoufo Ponou, Madan Poka, Patrick H. Demana, Rémy B. Teponno, and Léon Azefack Tapondjou. "Ethnobotany, Phytochemistry, and Biological Activities of the Genus Cordyline." Biomolecules 13, no. 12 (December 12, 2023): 1783. http://dx.doi.org/10.3390/biom13121783.

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Cordyline species have a long history in traditional medicine as a basis of treatment for various ailments such as a bloody cough, dysentery, and a high fever. There are about 26 accepted species names in this genus distributed worldwide, including C. fruticosa, C. autralis, C. stricta, C. cannifolia, and C. dracaenosides. This work presents a comprehensive review of the traditional uses of plants of the genus Cordylie and their chemical constituents and biological activities. A bibliographic search was conducted to identify available information on ethnobotany, ethnopharmacology, chemical composition, and biological activities. A total of 98 isolated compounds potentially responsible for most of the traditional medicinal applications have been reported from eight species of Cordyline and are characterised as flavonoid, spirostane, furostane, and cholestane glycosides. Some of these pure compounds, as well as extracts from some species of Cordyline, have exhibited noteworthy anti-oxidant, antiproliferative, antimicrobial, and hypolipidemic activities. Although many of these species have not yet been investigated phytochemically or pharmacologically, they remain a potential source of new bioactive compounds.

35

Sharma, Meenakshi, Inderpreet Dhaliwal, Kusum Rana, Anil Kumar Delta, and Prashant Kaushik. "Phytochemistry, Pharmacology, and Toxicology of Datura Species—A Review." Antioxidants 10, no. 8 (August 15, 2021): 1291. http://dx.doi.org/10.3390/antiox10081291.

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Datura, a genus of medicinal herb from the Solanaceae family, is credited with toxic as well as medicinal properties. The different plant parts of Datura sp., mainly D. stramonium L., commonly known as Datura or Jimson Weed, exhibit potent analgesic, antiviral, anti-diarrheal, and anti-inflammatory activities, owing to the wide range of bioactive constituents. With these pharmacological activities, D. stramonium is potentially used to treat numerous human diseases, including ulcers, inflammation, wounds, rheumatism, gout, bruises and swellings, sciatica, fever, toothache, asthma, and bronchitis. The primary phytochemicals investigation on plant extract of Datura showed alkaloids, carbohydrates, cardiac glycosides, tannins, flavonoids, amino acids, and phenolic compounds. It also contains toxic tropane alkaloids, including atropine, scopolamine, and hyoscamine. Although some studies on D. stramonium have reported potential pharmacological effects, information about the toxicity remains almost uncertain. Moreover, the frequent abuse of D. stramonium for recreational purposes has led to toxic syndromes. Therefore, it becomes necessary to be aware of the toxic aspects and the potential risks accompanying its use. The present review aims to summarize the phytochemical composition and pharmacological and toxicological aspects of the plant Datura.

36

Bilia, Anna Rita. "1968–2008: 40 Years of Franco F. Vincieri's Natural Products Research." Natural Product Communications 3, no. 12 (December 2008): 1934578X0800301. http://dx.doi.org/10.1177/1934578x0800301201.

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This paper presents an overview of Prof. Vincieri's accomplishments in his career as a researcher in the field of pharmacognosy (pharmaceutical biology), analytical phytochemistry and pharmaceutical technology applied to herbal drug preparations at the Department of Pharmaceutical Sciences of the University of Florence. This article is a recognition of his valuable contributions to these research fields, especially for his outstanding and innovative interdisciplinary studies on the quality control of herbal drugs, herbal drug preparations, herbal medicinal products, botanical food supplements, and some “special foods” such as grapes, wines, olives and olive oil.

37

Thanikachalam, Varalakshmi, and Indira A. Jayaraj. "Phytochemistry of Amaranthus viridis: GC-MS Analysis." International Journal of Current Research and Review 13, no. 07 (2021): 162–66. http://dx.doi.org/10.31782/ijcrr.2021.13713.

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38

NORMASIWI, Suluh, Siti S. HAFIZHAH, Ida ADVIANY, and Muhammad I. SURYA. "Evaluation of reproduction biology of Prunus cerasoides." Notulae Scientia Biologicae 15, no. 3 (September 7, 2023): 11601. http://dx.doi.org/10.55779/nsb15311601.

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Prunus cerasoides have a high value in phytochemistry and pharmacology. It was classified as the Least Concern globally based on the IUCN red list due to its widespread distribution in eastern Asia. This research aims to evaluate the reproductive biology of P. cerasoides through the study of pollen morphology, pollen viability, stigma receptivity, and pollination in the Cibodas Botanical Garden, located in the Cibodas subdistrict of West Java, Indonesia. The pollen morphology was observed using SEM. Moreover, the pollen viability test was followed by the staining method (aceto-orcein 2%, I2KI 1%, TTC 1%) and in vitro pollen germination with thirteen treatments (aquadest [control]; 5-30% sucrose; and 5-30% sucrose + 5 ppm boric acid). Stigma receptivity was observed daily, from 7 days before anthesis until the anthesis stage. Furthermore, several types of pollination were evaluated, including open pollination, autogamy, geitonogamy, and allogamy. The results showed that the best staining method on P. cerasoides was aceto-orcein 2%, with pollen viability at 87.87%. The sucrose concentration of 25% at 72 hours of observation gave the highest pollen viability results, 52.48%. Stigma receptivity was optimal in the two days before anthesis until anthesis. The highest pollination efficiency was cross-pollination at 53.33%, with an average percentage of the total fruit set of 24.17%.

39

Ranghoo-Sanmukhiya, Mala, Joyce Govinden-Soulange, Christophe Lavergne, Shannoo Khoyratty, Denis Da Silva, Michel Frederich, and Hippolyte Kodja. "Molecular biology, phytochemistry and bioactivity of three endemic Aloe species from Mauritius and Réunion Islands." Phytochemical Analysis 21, no. 6 (September 7, 2010): 566–74. http://dx.doi.org/10.1002/pca.1234.

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40

Akaberi, Toktam, Kamran Shourgashti, Seyed Ahmad Emami, and Maryam Akaberi. "Phytochemistry and pharmacology of alkaloids from Glaucium spp." Phytochemistry 191 (November 2021): 112923. http://dx.doi.org/10.1016/j.phytochem.2021.112923.

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41

Marston, Andrew. "Role of advances in chromatographic techniques in phytochemistry." Phytochemistry 68, no. 22-24 (November 2007): 2786–98. http://dx.doi.org/10.1016/j.phytochem.2007.08.004.

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42

Bolwell, G. Paul. "Phytochemistry in the Genomics and Post-Genomics Eras." Phytochemistry 63, no. 1 (May 2003): 123. http://dx.doi.org/10.1016/s0031-9422(03)00002-5.

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43

Harborne, Jeffrey B. "The phytochemistry of the horticultural plants of Qatar." Phytochemistry 30, no. 7 (January 1991): 2451. http://dx.doi.org/10.1016/0031-9422(91)83685-e.

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44

Shekhawat, Dr Neha. "Guazuma Ulmifolia: A Review on its Traditional Uses, Phytochemistry and Pharmacology." International Journal of pharma and Bio Sciences 12, no. 2 (April 13, 2021): 93–105. http://dx.doi.org/10.22376/ijpbs.2021.12.2.b93-105.

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45

Al-Awthan, Yahya S., and Omar Salem Bahattab. "Phytochemistry and Pharmacological Activities of Dracaena cinnabari Resin." BioMed Research International 2021 (July 22, 2021): 1–7. http://dx.doi.org/10.1155/2021/8561696.

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Dracaena cinnabari (D. cinnabari) is an endemic plant located in Socotra Island, Yemen. Deep red resin attained from different plant species including D. cinnabari is commonly known as dragon’s blood. In folk medicine, it is prescribed for the treatment of traumatic dermal, dental, and eye injuries as well as blood stasis, pain, and gastrointestinal diseases in humans. Numerous studies have investigated that this resinous medicine has antidiarrheal, antiulcer, antimicrobial, antiviral, antitumor, anti-inflammatory, analgesic, wound healing, and antioxidant activity. Several phytochemicals have been isolated from D. cinnabari, including the biflavonoid cinnabarone, triflavonoids, metacyclophanes, chalcones, chalcanes, dihydrochalcones, sterols, and terpenoids. The present review highlights the structures and bioactivities of main phytochemicals isolated from D. cinnabari regarding the botany and pharmacological effects of the resin derived from this plant.

46

Gangwar, Mayank, R. K. Goel, and Gopal Nath. "Mallotus philippinensisMuell. Arg (Euphorbiaceae): Ethnopharmacology and Phytochemistry Review." BioMed Research International 2014 (2014): 1–13. http://dx.doi.org/10.1155/2014/213973.

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Mallotus philippinensisMuell. Arg (Euphorbiaceae) are widely distributed perennial shrub or small tree in tropical and subtropical region in outer Himalayas regions with an altitude below 1,000 m and are reported to have wide range of pharmacological activities.Mallotus philippinensisspecies are known to contain different natural compounds, mainly phenols, diterpenoids, steroids, flavonoids, cardenolides, triterpenoids, coumarins, isocoumarins, and many more especially phenols; that is, bergenin, mallotophilippinens, rottlerin, and isorottlerin have been isolated, identified, and reported interesting biological activities such as antimicrobial, antioxidant, antiviral, cytotoxicity, antioxidant, anti-inflammatory, immunoregulatory activity protein inhibition against cancer cell. We have selected all the pharmacological aspects and toxicological and all its biological related studies. The present review reveals thatMallotus philippinensisis a valuable source of medicinally important natural molecules and provides convincing support for its future use in modern medicine. However, the existing knowledge is very limited aboutMallotus philippinensisand its different parts like steam, leaf, and fruit. Further, more detailed safety data pertaining to the acute and subacute toxicity and cardio- and immunotoxicity also needs to be generated for crude extracts or its pure isolated compounds. This review underlines the interest to continue the study of this genus of the Euphorbiaceae.

47

Dalli, Mohammed, Oussama Bekkouch, Salah-eddine Azizi, Ali Azghar, Nadia Gseyra, and Bonglee Kim. "Nigella sativa L. Phytochemistry and Pharmacological Activities: A Review (2019–2021)." Biomolecules 12, no. 1 (December 23, 2021): 20. http://dx.doi.org/10.3390/biom12010020.

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Abstract:

Medicinal and aromatic plants are mainly characterized by the presence of different bioactive compounds which exhibit various therapeutic activities. In order to investigate the different pharmacological properties of different Nigella sativa extracts, a multitude of research articles published in the period between 2019 and 2021 were obtained from different databases (Scopus, Science Direct, PubMed, and Web of Science), and then explored and analyzed. The analysis of the collected articles allows us to classify the phytochemicals and the pharmacological activities through their underlying molecular mechanisms, as well as to explore the pharmacological activities exhibited by several identified compounds in Nigella sativa which allow a better understanding, and better elucidation, of the bioactive compounds responsible for the pharmacological effects. Also shown are the existence of other bioactive compounds that are still unexplored and could be of great interest. This review could be taken as a guide for future studies in the field.

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Han, Shuang, Ling-zhi Li, and Shao-jiang Song. "Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses." Phytochemistry 171 (March 2020): 112231. http://dx.doi.org/10.1016/j.phytochem.2019.112231.

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Lewis, Norman G. "G.H. Neil Towers (1923–2004) Phytochemistry Pioneer – In Memoriam." Phytochemistry 68, no. 14 (July 2007): 1834–37. http://dx.doi.org/10.1016/j.phytochem.2007.05.008.

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Jain, Mahendra, Rakhee Kapadia, Ravirajsinh Navalsinh Jadeja, Menaka Chanu Thounaojam, Ranjitsinh Vijaysinh Devkar, and Shri Hari Mishra. "Traditional uses, phytochemistry and pharmacology of Tecomella undulata– A review." Asian Pacific Journal of Tropical Biomedicine 2, no. 3 (January 2012): S1918—S1923. http://dx.doi.org/10.1016/s2221-1691(12)60521-8.

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