The DOI matches its Crossref record; 150 of the 166 references it cites were found in a registry or an index.
Phytoecdysteroids: biological aspects
Abstract
Phytoecdysteroids are a family of about 200 plant steroids related in structure to the invertebrate steroid hormone 20-hydroxyecdysone. Typically, they are C27, C28 or C29 compounds possessing a 14alpha-hydroxy-7-en-6-one chromophore and A/B-cis ring fusion (5beta-H). In the present review, the distribution, biosynthesis, biological significance and potential applications of phytoecdysteroids are summarised.
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“research results suggest that only around 6% of plant species contain detectable levels of PEs [6,8,9,10].”
From Ecdysterone and Turkesterone—Compounds with Prominent Potential in Sport and Healthy Nutrition (2024) · cites this paper as [8]
In the citing paper
“However, variations exist regarding the levels of 20HE in spinach, with some reporting lower amounts, such as 50 μg/g dry mass, 10.3 and 16.8 μg/g in different spinach accessions, and 0.44 mg% dry weight [8,156,160].”
From Ecdysterone and Turkesterone—Compounds with Prominent Potential in Sport and Healthy Nutrition (2024) · cites this paper as [8]
In the citing paper
“The biosynthetic pathway(s) in plants, just like that in arthropods, has not yet been fully elucidated, but the biosynthesis appears to differ mechanistically from that in animals (Figure 7), and maybe also differ within types of plant (e.g., between angiosperms and ferns; [3,35])”
From Ecdysteroids (2021) · cites this paper as [35]
In the citing paper
“The huge diversity of phytoecdysteroid molecular structures indicates that biosynthesis in plants occurs as a combinatorial system of a network of enzymes without strong substrate specificity, which could result in over 1000 possible permutations of structure from a small number of early intermediates (14α-hydroxy-6-oxo-7-ene C 27/28/29sterols [35]).”
From Ecdysteroids (2021) · cites this paper as [35]
In the citing paper
“It has been shown in several ecdysteroid-accumulating species that ecdysteroid levels are additionally influenced by environmental factors (e.g., temperature, nutritional factors, invertebrate predation [35]).”
From Ecdysteroids (2021) · cites this paper as [35]
In the citing paper
“Both E and 20E exist in plants to play roles in the plants or participate in the defense of plants against insects [73].”
From G protein-coupled receptors function as cell membrane receptors for the steroid hormone 20-hydroxyecdysone (2020) · cites this paper as [73]
In the citing paper
“A series of evidence suggests that PEs do not accumulate in the majority of plant species as the expression of the biosynthetic pathways in plants is downregulated6.”
From The Phytochemical, Biological, and Medicinal Attributes of Phytoecdysteroids: An Updated Review (2021) · cites this paper as [6]
In the citing paper
“a survey indicates that only ∼6% of all plants contain detectable levels of ecdysteroids6.”
From The Phytochemical, Biological, and Medicinal Attributes of Phytoecdysteroids: An Updated Review (2021) · cites this paper as [6]
In the citing paper
“PEs have several beneficial effects on mammals: they play roles in anabolic, adaptogenic, antidiabetic, anti-inflammatory, antioxidant, antitumor, antimicrobial, and anti-arthritic activity. They also act as hepatoprotectors and immunomodulators [3,8,12,15,155].”
From Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones (2022) · cites this paper as [3]
In the citing paper
“PE treatment negatively affects invertebrate growth, development, and reproduction, but PEs do not exhibit toxicity in mammals [3].”
From Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones (2022) · cites this paper as [3]
In the citing paper
“Ecdysteroids exhibit interesting pharmacological effects on mammals, such as the stimulation of protein synthesis, antidiabetic activity, and antirheumatic activity [5,6,7].”
In the citing paper
“Ecdysteroids are a,b-unsaturated 6-ketosteroids that occur in a wide range of plant species; as analogs of the insect molting hormone ecdysone, these compounds possess several biological functions in the flora and the fauna [11,12].”
From Nitrogen-containing ecdysteroid derivatives vs. multi-drug resistance in cancer: Preparation and antitumor activity of oximes, oxime ethers and a lactam (2018) · cites this paper as [11]
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“Commonly known IGRs are insect developmental hormone agonists that mimic the actions of juvenile hormone and ecdysone while others inhibit chitin synthesis [55, 56].”
BackgroundLignan Glucosides and Serotonin Phenylpropanoids from the Seeds of Leuzea carthamoides
Harmatha, J., Buděšı́nský, M., Vokáč, K., Pavlı́k, M., Grüner, K., & Laudová, V. (2007) · Collection of Czechoslovak Chemical Communications · doi:10.1135/cccc20070334 · Cited by 31
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“20-hydroxyecdysone (20E) is the most commonly occurring and the most abundant phytoecdysteroids produced by plants (Lafont, 1997; Dinan, 2001).”
BackgroundShuvalov, O., Fedorova, O., Tananykina, E., Gnennaya, Y., Daks, A., Petukhov, A., & Barlev, N. A. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.561537 · Cited by 30
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“At the same time, when arthropods eat plants containing phytoecdysteroids, they can suffer from various disorders (metabolic stress, premature molt, weight loss, etc.) up to their death; i.e., these substances perform an active safety function (Dinan, 2001; Timofeev, 2006).”
BackgroundLim, H.-S., Moon, B. C., Lee, J., Choi, G., & Park, G. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.07.010 · Cited by 30
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“The bases are 20-hydroxyecdysone and have 14 α-hydroxy-7-ene-6-one chromophores fused with a/B-cis ring (5 β-H) in their chemical structures (Dinan 2001).”
Background24-Epibrassinolide and 20-hydroxyecdysone affect photosynthesis differently in maize and spinach
Rothová, O., Hola, D., Kočová, M., Tůmová, L., Hnilička, F., Hniličková, H., Kamlar, M., & Macek, T. (2014) · Steroids · doi:10.1016/j.steroids.2014.04.006 · Cited by 29
C-29 Ecdysteroids from Ajuga reptans var. reptans
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Phytoecdysteroids from the Roots of Achyranthes bidentata Blume
Zhang, M., Zhou, Z., Wang, J., Cao, Y., Chen, X., Zhang, W., Lin, L., & Tan, J. (2012) · Molecules · doi:10.3390/molecules17033324 · Cited by 28
“3 and Tables 1 and 2) supported the fact that 1 was an ecdysteroid closely related to inokosterone-20,22-acetonide, a reported [21,22] ecdysteroid compound which was also obtained as compound 3 in the present study.”
BackgroundProapoptotic and proautophagic activity of 20-hydroxyecdysone in breast cancer cells in vitro
Romaniuk-Drapała, A., Lisiak, N., Totoń, E., Matysiak, A., Nawrot, J., Nowak, G., Kaczmarek, M., Rybczyńska, M., & Rubiś, B. (2021) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2021.109479 · Cited by 27
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“They can be found in plant families comprising ferns, gymnosperms and angiosperms [1].”
Kapare, V., Satdive, R., Fulzele, D. P., & Malpathak, N. (2017) · Journal of Plant Growth Regulation · doi:10.1007/s00344-017-9697-3 · Cited by 27
“20HE is metabolically stable and found in a variety of plant families and participates in plant defenses against herbivorous insects, rather than as a phytohormonal role (Schmelz and others 2000; Dinan 2001). Gamma rays are ionizing radiation, and high doses are harmful due to the generation of free radicals which cau…”
BackgroundEcdysterone and its Activity on some Degenerative Diseases
Cahlíková, L., Macáková, K., Chlebek, J., Hošťálková, A., Kulhánková, A., & Opletal, L. (2011) · Natural Product Communications · doi:10.1177/1934578x1100600527 · Cited by 26
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9α,20-Dihydroxyecdysone, a New Natural Ecdysteroid from Silene italica ssp. nemoralis
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Level and distribution of 20-hydroxyecdysone during Pfaffia glomerata development
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Plant Steroids: Occurrence, Biological Significance and their Analysis
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Low-polarity phytoecdysteroids from the juice of Serratula coronata L. (Asteraceae)
Odinokov, V. N., Kumpun, S., Galyautdinov, I. V., Evrard-Todeschi, N., Veskina, N. A., Khalilov, L. M., Girault, J.-P., Dinan, L., Maria, A., & Lafont, R. (2005) · Collection of Czechoslovak Chemical Communications · doi:10.1135/cccc20052038 · Cited by 23
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“Plants from the genera Leuzea (Rhaponticum), Serratula, Cyanotis, and Pfaffia are among those known to contain high amounts of PEs (Dinan, 2001; Lafont and Dinan, 2003).”
BackgroundEcdysteroid metabolism in mammals: The fate of ingested 20-hydroxyecdysone in mice and rats
Dinan, L., Balducci, C., Guibout, L., Foucault, A.-S., Bakrim, A., Kumpun, S., Girault, J.-P., Tourette, C., Dioh, W., Dilda, P. J., et al. (2021) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2021.105896 · Cited by 23
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“In general, important tissues/organs for plant survival contain a higher concentration of phytoecdysteroids, which is probably due to the protective effect of these compounds against insects (Dinan 2001; Klein 2004). Interestingly, Festucci-Buselli et al. (2008) recently reported that the stem and leaf total of 20-hyd…”
BackgroundInfluentialThree new steroids from the roots of Serratula wolffii
Simon, A., Tóth, G., Liktor‐Busa, E., Kele, Z., Takács, M., Gergely, A., & Báthori, M. (2007) · Steroids · doi:10.1016/j.steroids.2007.06.004 · Cited by 23
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Harada, T., Nakagawa, Y., Akamatsu, M., & Miyagawa, H. (2009) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2009.07.011 · Cited by 23
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“Instead, it is predicted that phytoecdysteroids induce precocious molting and subsequently death in insects providing an effective defense against insect feeding [22].”
InfluentialKumar, R. P., Babu, K. V. D., & Da, E. (2018) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2018.11.018 · Cited by 22
Uawisetwathana, U., Chevallier, O. P., Yun Xu, A., Kamolsukyeunyong, W., Nookaew, I., Somboon, T., Toojinda, T., Vanavichit, A., Goodacre, R., Elliott, C. T., et al. (2019) · Metabolomics · doi:10.1007/s11306-019-1616-0 · Cited by 23
“Secondly, 20-hydroxyecdysone acetate is a phytoecdysteroid synthesized by plants for defense against phytophagous insects (Adler and Grebenok 1999; Dinan 2001).”
BackgroundBiosynthesis of Triterpenoid Natural Products
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“PE biosynthesis and transport in developing spinach had a continuous redistribution within the growing plant between ‘source’ older leaves and young, developing ‘sinks’ leaves.5 Spinach PE synthesis showed direct negative feedback of the major PE, 20E.5 Biomedical applications of PEs.”
BackgroundInfluentialIshola, I. O., Ochieng, C. O., Olayemi, S. O., Jimoh, M. O., & Lawal, S. M. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2014.11.005 · Cited by 22
“Interestingly, ecdysteroids stimulate protein synthesis without thymolytic, anti-gonadotropic, or androgenic side effect (Dinan, 2001; Meena et al., 2010).”
Guan, H., Chi, D., Yu, J., & Li, H. (2010) · Chemical Engineering Journal · doi:10.1016/j.cej.2010.12.040 · Cited by 22
Supercritical fluid extraction of cynaropicrin and 20‐hydroxyecdysone from Leuzea carthamoides DC
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Phytoecdysteroids and other constituents from the roots of Klaseopsis chinensis
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“These insects develop normally on diets with up to 400 ppm 20-hydroxyecdysone (Dinan, 2001).”
BackgroundInfluentialDistribution and Biosynthesis of 20-Hydroxyecdysone in Plants ofAchyranthes japonicaNakai
Boo, K.-H., Lee, D., Jeon, G. L., Ko, S. H., Cho, S. K., Kim, J. H., Park, S., Hong, Q. C., Lee, S., Lee, D., et al. (2010) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.100410 · Cited by 21
Side-chain cleaved phytoecdysteroid metabolites as activators of protein kinase B
Issaadi, H. M., Csábi, J., Hsieh, T., Gáti, T., Tóth, G., & Hunyadi, A. (2018) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2018.10.049 · Cited by 22
“The A/B ring junction is normally cis, whereas the B/C and C/D ring junctions are almost always trans [2].”
BackgroundNew Minor Ecdysteroids from Silene viridiflora
Mamadalieva, N. Z., Zibareva, L. N., Evrard‐Todeschi, N., Girault, J., Maria, A., Ramazanov, N. S., Saatov, Z., & Lafont, R. (2004) · Collection of Czechoslovak Chemical Communications · doi:10.1135/cccc20041675 · Cited by 21
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Fang, L., Li, J., Zhou, J., Wang, X., & Guo, L. (2017) · Molecules · doi:10.3390/molecules22081310 · Cited by 20
Issaadi, H. M., Tsai, Y.-C., Chang, F.-R., & Hunyadi, A. (2017) · Journal of Chromatography B · doi:10.1016/j.jchromb.2017.03.043 · Cited by 19
Báthori, M., Kalász, H., Pongrácz, Z., Máthé, I., Kálmán, A., & Argay, G. (2002) · Biomedical Chromatography · doi:10.1002/bmc.168 · Cited by 19
20-Hydroxyecdysone protects wheat seedlings (Triticum aestivum L.) against lead stress
Lamhamdi, M., Lafont, R., Rharrabe, K., Sayah, F., Aarab, A., & Bakrim, A. (2016) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2015.11.006 · Cited by 18
Céspedes, C. L., Lina-García, L. P., Kubo, I., Salazar, J. R., Ariza‐Castolo, A., Alarcón, J., Aqueveque, P. M., Werner, E., & Seigler, D. S. (2016) · Industrial Crops and Products · doi:10.1016/j.indcrop.2016.05.026 · Cited by 18
Effects of ecdysteroids on Chlorella vulgaris
Bajguz, A., & Dinan, L. (2004) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2004.00329.x · Cited by 17
Ecdysteroids from the flowers of Aerva javanica
Saleem, M., Musaddiq, S., Riaz, N., Zubair, M., Ashraf, M., Nasar, R., & Jabbar, A. (2013) · Steroids · doi:10.1016/j.steroids.2013.07.012 · Cited by 17
Li, D., Zhang, Y., Cui, Z., He, L., Chen, W., Meng, Q., & Ren, L. (2016) · PLoS ONE · doi:10.1371/journal.pone.0153584 · Cited by 17
“The main zoo-ecdysteroid is 20-hydroxyecdysone (20E), which is recognized as the most biologically active ecdysteroid [9].”
BackgroundBatista, D. S., Koehler, A. D., Romanel, E. A. D. C., Souza, V., Silva, T. D., Almeida, M. C., Maciel, T. E. F., Ferreira, P. R. B., Felipe, S. H. S., Saldanha, C. W., et al. (2018) · PROTOPLASMA · doi:10.1007/s00709-018-1322-1 · Cited by 17
Ajaha, A., Bouayad, N., Aarab, A., & Rharrabe, K. (2019) · Journal of Insect Science · doi:10.1093/jisesa/iez097 · Cited by 19
“Phytoecdysteroids were found to have defensive potential against pests’s attacks (Dinan 2001, Schmelz et al.”
BackgroundMethodPhytoecdysteroids: Phytochemistry and Pharmacological Activity
Laekeman, G., & Vlietinck, A. J. (2013) · Springer eBooks · doi:10.1007/978-3-642-22144-6_173 · Cited by 17
Pavela, R., Harmatha, J., Bárnet, M., & Vokáč, K. (2005) · European Journal of Entomology · doi:10.14411/eje.2005.091 · Cited by 17
Innovative and Future Applications for Ecdysteroids
Lafont, R., & Dinan, L. N. (2009) · Springer eBooks · doi:10.1007/978-1-4020-9112-4_23 · Cited by 17
“Although ecdysteroids are present in seeds of ca. 6% of all investigated plant species ( Dinan, 2001 ), significant amounts of them have been detected in only a few food plants (Table 23.3), possibly because cultivated plants have been selected for productivity and have therefore lost their ability to produce secondar…”
BackgroundInfluentialAmbrosio, G., Yuliandra, T., Wuest, B., Mazzarino, M., Torre, X. D. L., Botrè, F., Diel, P., Isenmann, E., & Parr, M. K. (2021) · doi:10.20944/preprints202105.0106.v1 · Cited by 14
“Moreover, growth-promoting and anabolic effects in animals and in humans have been reported [3-19].”
BackgroundBathori, M., Pongracz, Z., Toth, G., Simon, A., Kandra, L., Kele, Z., & Ohmacht, R. (2002) · Journal of Chromatographic Science · doi:10.1093/chromsci/40.7.409 · Cited by 23
John, R., Shajitha, P. P., Devassy, A., & Mathew, L. (2018) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-018-0506-7 · Cited by 16
“The most common phytoecdysteroid is 20-hydroxyecdysone and it has potential therapeutic applications (Dinan 2001) and several agricultural applications.”
Preston-Mafham, J., & Dinan, L. (2002) · Zeitschrift für Naturforschung C · doi:10.1515/znc-2002-1-224 · Cited by 18
“A range of evidence now exists in support of this hypothesis (summarised in Dinan, 1998; 2001).”
BackgroundThe Use of Plant Steroids in Viral Disease Treatments: Current Status and Future Perspectives
Yerlikaya, P. O., Arısan, E. D., Mehdizadehtapeh, L., Onganer, P. U., & Gürkan, A. Ç. (2023) · European Journal of Biology · doi:10.26650/eurjbiol.2023.1130357 · Cited by 16
Meng, Y.-H., Whiting, P., Šik, V., Rees, H. H., & Dinan, L. N. (2001) · Zeitschrift für Naturforschung C · doi:10.1515/znc-2001-11-1214 · Cited by 16
Salazar, J. R., Loza-Mejía, M. A., & Soto-Cabrera, D. (2020) · Molecules · doi:10.3390/molecules25071649 · Cited by 16
“were included in the present review because of the special feature of the configuration 5β in a sterol configuration, an infrequent feature in cacti sterols [52], but common in ecdysteroids and related phytoecdysteroids [53,54].”
BackgroundWatanabe, M., Miyashita, T., & Devkota, H. P. (2020) · Biochemical Systematics and Ecology · doi:10.1016/j.bse.2020.104211 · Cited by 16
Yang, S., Zhang, X., Sun, X.-S., Ling, T.-J., Feng, Y., Du, X., Zhao, M., Yang, Y., Xue, D., Wang, L., et al. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-100621 · Cited by 16
“However, ECRs exhibit extremely high structural diversity, especially in the number, position, and orientation of hydroxyl groups as well as in the variety of long carbon side chains [13], resulting in different effects on A β aggregation and cytotoxicity.”
InfluentialRagged Robin (Lychnis flos-cuculi) - a plant with potential medicinal value
Maliński, M. P., Michalska‐Falkowska, A., Tomczykowa, M., Tomczyk, M., & Thiem, B. (2014) · Revista Brasileira de Farmacognosia · doi:10.1016/j.bjp.2014.11.004 · Cited by 16
Kayani, W. K., Palazón, J., Cusido, R. M., & Mirza, B. (2016) · RSC Advances · doi:10.1039/c6ra00250a · Cited by 15
Neves, C. S., Gomes, S. S. L., dos Santos, T. R., de Almeida, M. M., de Souza, Y. O., Garcia, R. M. G., Otoni, W. C., Chedier, L. M., Raposo, N. R. B., Viccini, L. F., et al. (2016) · South African Journal of Botany · doi:10.1016/j.sajb.2016.07.003 · Cited by 16
Muchate, N. S., Rajurkar, N. S., Suprasanna, P., & Nikam, T. D. (2018) · International Journal of Phytoremediation · doi:10.1080/15226514.2018.1452184 · Cited by 16
“Ecdysteroids which are triterpenoid compounds play significant biological activities (Dinan 2001).”
BackgroundDereplication and Partial Identification of Compounds
Dinan, L. N. (2006) · Humana Press eBooks · doi:10.1385/1-59259-955-9:297 · Cited by 17
Synthesis and biological activities of turkesterone 11α-acyl derivatives
Dinan, L. N., Bourne, P. C., Whiting, P., Tsitsekli, A., Saatov, Z., Dhadialla, T. S., Hormann, R. E., Lafont, R., & Coll, J. (2003) · Journal of Insect Science · doi:10.1093/jis/3.1.6 · Cited by 16
Thussagunpanit, J., Jutamanee, K., Homvisasevongsa, S., Suksamrarn, A., Yamagami, A., Nakano, T., & Asami, T. (2017) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2017.05.003 · Cited by 15
“Ecdysteroids are generally known as compounds that regulate molting and metamorphosis in insects and crustaceans [12, 13], but various plant species also produce these compounds (phytoecdysteroids), which are widely thought to inhibit the feeding of phytophagous insects [12].”
Agoun, H., Semiane, N., Mallek, A., Bellahreche, Z., Hammadi, S., Madjerab, M., Abdlalli, M., Khalkhal, A., & Dahmani, Y. (2021) · Archives of Physiology and Biochemistry · doi:10.1080/13813455.2019.1621350 · Cited by 15
“Phytoecdysteroids are a large family of polyhydroxylated steroids related to insect moulting hormones, that are produced by many plant species (Dinan 2001), including a few cultivated crops (e.g. spinach, quinoa).”
BackgroundMuchate, N. S., Kadam, N. S., Rajurkar, N. S., & Nikam, T. D. (2017) · Journal of Planar Chromatography – Modern TLC · doi:10.1556/1006.2017.30.3.7 · Cited by 15
Duan, H., Yang, X. L., Bu, Z., Li, X., Zhang, Z., & Sun, W. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00508 · Cited by 15
“Since the isolation of ecdysone from silkworm pupae in 1954, ecdysteroid analogs called phytoecdysteroids were also discovered in plant species (Butenandt and Karlson, 1954; Nakanishi et al., 1966; Lafont and Horn, 1989; Dinan, 2001).”
BackgroundPreclinical evaluation of safety and potential of black hellebore extracts for cancer treatment
Felenda, J. E., Turek, C., Mörbt, N., Herrick, A., Müller, M., & Stintzing, F. C. (2019) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-019-2517-5 · Cited by 15
Felipe, S. H. S., Batista, D. S., Chagas, K., Correia, L. N. F., Silva, T. D., Fortini, E. A., Silva, P. O., & Otoni, W. C. (2019) · PROTOPLASMA · doi:10.1007/s00709-019-01400-3 · Cited by 15
“In mammals, they are not biosynthesized but show medicinal effects, especially for humans (Dinan 2001; Báthori and Pongrácz 2005; Dinan and Lafont 2006; Thiem et al. 2017; Dias et al. 2019).”
BackgroundRostagno, M., Debien, I. C. N., Vardanega, R., Nogueira, G. C., Barbero, G., & Meireles, M. (2014) · Analytical Methods · doi:10.1039/c3ay42276c · Cited by 15
Dinan, L., Balducci, C., Guibout, L., & Lafont, R. (2020) · Phytochemical Analysis · doi:10.1002/pca.2930 · Cited by 14
Napierała, M., Nawrot, J., Gornowicz-Porowska, J., Florek, E., Moroch, A., Adamski, Z., Kroma, A., Miechowicz, I., & Nowak, G. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17186453 · Cited by 14
A new ecdysteroid and other constituents from two Dioscorea species
Sautour, M., Canon, F., Miyamoto, T., Dongmo, A., & Lacaille-Dubois, M.-A. (2008) · Biochemical Systematics and Ecology · doi:10.1016/j.bse.2008.03.002 · Cited by 17
Kamada, T., Picoli, E. A. D. T., Vieira, R. F., Barbosa, L. C. A., Cruz, C. D., & Otoni, W. C. (2009) · Revista Brasileira de Plantas Medicinais · doi:10.1590/s1516-05722009000300004 · Cited by 14
Laurent, P., Braekman, J. C., Daloze, D., & Pasteéls, J. M. (2003) · Chemoecology · doi:10.1007/s00049-003-0235-3 · Cited by 14
“They are often present in high concentrations ( Dinan, 2001 ).”
BackgroundPhytoecdysteroids: A Novel, Non-Androgenic Alternative for Muscle Health and Performance
McBride, J. M. (2013) · Journal of Steroids & Hormonal Science · doi:10.4172/2157-7536.s12-e001 · Cited by 15
“In general, PEs are characterized as polyhydroxylated basic carbon ring structures of 27-29 carbon atoms [15].”
BackgroundInfluentialPreparative-Scale Chromatography of Ecdysteroids: A Class of Biologically Active Steroids
Toth, N., & Báthori, M. (2008) · Journal of Chromatographic Science · doi:10.1093/chromsci/46.2.111 · Cited by 14
Harmatha, J., Vokáč, K., Kmonı́čková, E., & Zı́dek, Z. (2008) · Steroids · doi:10.1016/j.steroids.2007.12.014 · Cited by 14
Todorova, V., Ivanov, K., Karcheva-Bahchevanska, D., & Ivanova, S. (2023) · Processes · doi:10.3390/pr11061786 · Cited by 13
Effect of 20-hydroxyecdysone on proteolytic regulation in skeletal muscle atrophy
HIRUNSAI, M., YIMLAMAI, T., & SUKSAMRARN, A. (2016) · In Vivo · doi:10.21873/invivo.11007 · Cited by 13
Marschall, M. J. M., Ringseis, R., Gessner, D. K., Grundmann, S. M., Most, E., Wen, G., Maheshwari, G., Zorn, H., & Eder, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105241 · Cited by 13
“While zooecdysteroids in insects regulate important developmental processes, such as embryogenesis, moulting (ecdysis), metamorphosis, reproduction, and diapause [1], phytoecdysteroids provide protection against invertebrate predators by acting as feeding deterrents and by disrupting critical developmental processes o…”
BackgroundCsábi, J., Martins, A., Sinka, I., Csorba, A., Molnár, J., Zupkó, I., Tóth, G., Tillekeratne, L. M. V., & Hunyadi, A. (2016) · MedChemComm · doi:10.1039/c6md00431h · Cited by 13
Metadata
- Authors
- Dinan, L.
- Affiliations
- University of Exeter (GB)
- Corresponding author
- Dinan, Laurence
- ORCID
- Dinan, Laurence
- Venue
- Phytochemistry
- Publisher
- Elsevier BV
- Published
- 2001-06
- Volume
- 57
- Issue
- 3
- Pages
- 325-339
- ISSN
- 0031-9422 (ISSN-L)
- OpenAlex
- W2032058270
- Cited by
- 392
- References
- 166
- Citations by year
- 2026: 17 · 2025: 11 · 2024: 11 · 2023: 13 · 2022: 18 · 2021: 27 · 2020: 23 · 2019: 18 · 2018: 18 · 2017: 18 · 2016: 18 · 2015: 13 · 2014: 17 · 2013: 15 · 2012: 19
- FWCI
- 0.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Phytochemistry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Phytochemical Studies and Bioactivities
- Physical Sciences › Chemistry › Organic Chemistry › Steroid Chemistry and Biochemistry
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
- Keywords
- phytoecdysteroids, 20-hydroxyecdysone, plant steroids, steroidogenesis, biological significance
- MeSH terms
- Animals, Ecdysone, Ecdysterone, Invertebrates, Pest Control, Biological, Phytosterols, Plant Physiological Phenomena
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