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Journal articles on the topic 'Corydine'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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1

Táborská, Eva, Milena Mikešová, František Věžník, and Jiří Slavík. "Alkaloids of the two Hypecoum L. species." Collection of Czechoslovak Chemical Communications 52, no. 2 (1987): 508–13. http://dx.doi.org/10.1135/cccc19870508.

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Alkaloids from Hypecoum procumbens L. and H. leptocarpum HOOK. F. et THOMS. were investigated. Protopine was the dominant alkaloid in both species. From H. procumbens chelerythrine and corydine were newly isolated in addition to the earlier detected alkaloids allocryptopine, sanguinarine, coptisine, and isocorydine. From H. leptocarpum allocryptopine, isocorydine and corydine were isolated for the first time, in addition to the earlier described alkaloids protopine, sanguinarine, chelerythrine and coptisine. Cryptopine was detected chromatographically. From the fraction of strongly polar alkal

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2

Singh, Deepika, and Prabir K. Chaudhuri. "(+) Corydine from the Stems of Tinospora cordifolia." Asian Journal of Chemistry 27, no. 4 (2015): 1567–68. http://dx.doi.org/10.14233/ajchem.2015.18509.

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3

Shafiee, Abbas, and Ata Jafarabadi. "Corydine and Norcorydine from the Roots ofChelidonium majus." Planta Medica 64, no. 05 (1998): 489. http://dx.doi.org/10.1055/s-2006-957498.

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4

Věžník, František, Irgash A. Israilov, Eva Táborská, and Jiří Slavík. "On alkaloids of three Papaver species from the section Scapiflora REICHB." Collection of Czechoslovak Chemical Communications 50, no. 8 (1985): 1745–52. http://dx.doi.org/10.1135/cccc19851745.

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The main alkaloid of the aerial part of P. croceum LEDEB. was nudaurine (I), isolated for the first time. In addition to amurine, known to be present in this species, oxysanguinarine (II) and corydine (IIIa) were also newly isolated and the presence of papaverrubine D demonstrated. In the fraction of tertiary bases from P.kerneri HAYEK allocryptopine and epialpinine (IV) were isolated as further alkaloids in addition to the already known alkaloids amurensine (the main alkaloid), amurensinine, amurine, alpinigenine, muramine, protopine, mecambridine, nudaurine, cryptopine and papaverrubines B,

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5

Chen, Chien-Kuang, Su-Chang Chen, Chung-Hsiung Chen, and Shoei-Sheng Lee. "Isoquinoline Alkaloids from the Leaves of Dehaasia Hainanensis." Natural Product Communications 2, no. 1 (2007): 1934578X0700200. http://dx.doi.org/10.1177/1934578x0700200115.

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This study was aimed at investigating the alkaloids present in the leaves of Dehaasia hainanensis. Thirteen isoquinolines were isolated and characterized. Of these, four aporphines [(+)-laurolitsine, (+)-corydine, (+)-laurotetanine and (+)-lindcarpine], two morphinans [(-)-sinoacutine and (-)-ocobotrine], four benzylisoquinolines [(+)-reticuline, (+)-roefractine, (+)-reticuline N-oxide, and O-methylarmepavine], and one bisbenzylisoquinoline [(-)-N,N'-dimethyllindoldhamine] are reported for the first time from Dehaasia species. The structures were elucidated by spectral analysis.

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6

Eric, Dade J. M., Coulibali Siomenan, Kouamé Bi Koffi François Prévost, et al. "A new natural indole and three aporphine alkaloids from Monodora bevipes Benth. (Annonaceae)." International Current Pharmaceutical Journal 6, no. 7 (2017): 40–43. http://dx.doi.org/10.3329/icpj.v6i7.34330.

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Four compounds were isolated from the leaves of Monodora brevipes Benth. (Annonaceae). Among them, one new natural indole named 5-formylindole (1) and three known aporphine alkaloids: (+)-roemeroline (2); (+)-corydine (3) and (+)-menispermine (4). They were isolated for the first time from this species. The structures of these compounds were established according to their spectral data (NMR, SM, IR and UV).Eric et al., International Current Pharmaceutical Journal, June 2017, 6(7): 40-43http://www.icpjonline.com/documents/Vol6Issue7/01.pdf

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7

O.J., Onoja, and Olawuni J.I. "DPPH Radical Scavenging Activity of Corydine Isolated from Tinospora cordifolia." African Journal of Pharmaceutical Sciences 3, no. 2 (2023): 68–78. http://dx.doi.org/10.51483/afjps.3.2.2023.68-78.

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8

OJOGBANE ONOJA, JOEL, та JULIUS IDOWU OLAWUNI. "β-SECRETASE INHIBITORY ACTIVITY OF CLERODANE DITERPENOIDS AND APORPHINOID ALKALOIDS AND INSIGHT FROM IN SILICO ANALYSES". AFRICAN JOURNAL OF PHARMACEUTICAL RESEARCH AND DEVELOPMENT 16, № 3 (2024): 80–86. https://doi.org/10.59493/ajopred/2024.3.9.

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The β-secretase, which is a β-site amyloid precursor protein cleaving enzyme 1 (BACE1), starts the synthesis of toxic amyloid β (Aβ), which is a key early factor in the pathophysiology of Alzheimer’s disease (AD). No cure for AD so far which necessitate the search for new neurotherapeutic agents especially from natural products (NPs). Inhibiting BACE1 using NP’s inhibitors is considered a promising strategy. The study aims to evaluate the BACE 1 inhibitory potentials of clerodane diterpenoids and aporphinoid alkaloids from the stem of Tinospora cordifolia (Willd.) Miers ex Hook. F. & Thoms

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9

Parvin, Mst Shamima, Jakub Chlebek, Anna Hošťálková, et al. "Interactions of Isoquinoline Alkaloids with Transition Metals Iron and Copper." Molecules 27, no. 19 (2022): 6429. http://dx.doi.org/10.3390/molecules27196429.

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Data on alkaloid interactions with the physiologically important transition metals, iron and copper, are mostly lacking in the literature. However, these interactions can have important consequences in the treatment of both Alzheimer’s disease and cancer. As isoquinoline alkaloids include galanthamine, an approved drug for Alzheimer’s disease, as well as some potentially useful compounds with cytostatic potential, 28 members from this category of alkaloids were selected for a complex screening of interactions with iron and copper at four pathophysiologically relevant pH and in non-buffered con

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10

Slavík, Jiří, and Leonora Slavíková. "Alkaloids from Papaver albiflorum PACZ. subsp. albiflorum and P. cf. stevenianum A. D. Mikheev." Collection of Czechoslovak Chemical Communications 55, no. 7 (1990): 1812–16. http://dx.doi.org/10.1135/cccc19901812.

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Papaver albiflorum PACZ. subsp. albiflorum (tetraploid, 2n = 28; total alkaloid content 0.001%) afforded corytuberine, protopine and allocryptopine as dominant alkaloids; in addition, small amounts of macambrine, thebaine, scoulerine, rhoeadine, papaverrubines D, C, A and E, berberine and coptisine were detected. Papaver cf. stevenianum A. D. MIKHEEV (hexaploid, 2n = 42; total alkaloid content 0.066% and 0.015%, respectively) gave berberine as the principal alkaloid (0.065% and 0.013, respectively) which was responsible for the yellow colour of latex. Corytuberine, allocryptopine, protopine an

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11

Slavíková, Leonora, Jiří Slavík, and Ladislav Dolejš. "Quaternary alkaloids from Glaucium oxylobum BOISS. et BUSHE." Collection of Czechoslovak Chemical Communications 50, no. 4 (1985): 854–60. http://dx.doi.org/10.1135/cccc19850854.

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From the fraction of quaternary alkaloids of the aerial part of Glaucium oxylobum BOISS. et BUSHE (-)-trans-N-rnethylcanadinium iodide was isolated as the main alkaloid after conversion to iodides, and, in a smaller amount, (+)-N-methylcorydinium iodide, detected for the first time in Papaveraceae, further (-)-trans-N-methylstylopinium iodide, magnoflorine iodide and a new quaternary alkaloid, N-methyldomesticinium iodide, isolated for the first time as a natural substance. In the roots, magnoflorine iodide accompanied by (+)-N-methylcorydinium iodide represented the main component of the quat

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12

Táborská, Eva, Jiří Dostál, Hana Bochořáková, and František Věžník. "Alkaloids of Papaver argemone L. and Papaver pavoninum FISCH. et MEY. From the Argemonorhoeades FEDDE section." Collection of Czechoslovak Chemical Communications 53, no. 8 (1988): 1845–50. http://dx.doi.org/10.1135/cccc19881845.

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Papaver argemone L. and Papaver pavoninum FISCH. et MEY. species of the Argemonorhoeades FEDDE (Papaveraceae) section were studied. A very low content of alkaloids was found in both species (less than 0·05%). P. argemone contains corytuberine and its quaternary N-methyl derivative magnoflorine as the dominant bases. As minor constituents were isolated: protopine, isocorydine, scoulerine, and alkaloids PAR 1, PAR 2, PAR 3. Chromatographic analysis detected allocryptopine, cryptopine, coptisine and traces of rhoeadine, papaverrubines C, D and E, and more than 6 unidentified bases. P. pavoninum g

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13

Táborská, Eva, Hana Bochořáková, František Věžník, Jiří Slavík, and Ladislav Dolejš. "Alkaloids from Papaver atlanticum BALL and Papaver glaucum BOISS. et HAUSKN." Collection of Czechoslovak Chemical Communications 51, no. 10 (1986): 2232–39. http://dx.doi.org/10.1135/cccc19862232.

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In addition to the alkaloids previously found in the aerial part of P. atlanticum BALL, viz. protopine, rhoeadine (predominant constituents), rhoeagenine, stylopine, cryptopine, sanguinarine, magnoflorine and papaverrubines A, B, E and D, we have now isolated the tertiary bases isothebaine, scoulerine, corytuberine and a new quaternary alkaloid 13β-hydroxy-N-methylstylopinium hydroxide (I). The presence of papaverrubine B and muramine was also detected (TLC). The contents of the bases in the roots of P. atlanticum were found similar to those in the aerial part. Magnoflorine was isolated from t

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14

KONDA, Yoshikazu, Yoshihiro IMAI, Hiroshi HOJO, Takeshi ENDO, and Shigeo NOZOE. "Suppression of tumor cell growth and mitogen response by aporphine alkaloids, dicentrine, glaucine, corydine, and apomorphine." Journal of Pharmacobio-Dynamics 13, no. 7 (1990): 426–31. http://dx.doi.org/10.1248/bpb1978.13.426.

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15

Slavík, Jiří, and Leonora Slavíková. "Alkaloids from Papaver bracteatum LINDL." Collection of Czechoslovak Chemical Communications 50, no. 5 (1985): 1216–26. http://dx.doi.org/10.1135/cccc19851216.

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N-Methylthebainium (as iodide) and corytuberine were isolated from the roots and green aerial parts of Papaver bracteatum LINDL., thebaine race Halle III, as significant alkaloids in addition to the predominant alkaloid thebaine (0.61 and 0.23% respectively), as well as the minor alkaloids isothebaine, scoulerine, protopine, epialpinine (O-methylalpinigenine), N-methylisothebainium (as iodide), isoboldine, corydine, rhoeadine, magnoflorine, a mixture of coptisine and palmatine and a new alkaloid PB 1 C18H19NO4. Bracteoline and papaverrubines G, E, D and C were detected chromatographically. Fro

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16

Slavík, Jiří, and Leonora Slavíková. "On alkaloids from the aerial parts of three Eschscholtzia species." Collection of Czechoslovak Chemical Communications 51, no. 8 (1986): 1743–51. http://dx.doi.org/10.1135/cccc19861743.

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In the aerial parts of Eschscholtzia californica CHAM., E. douglasii (HOOK. etARN.) WALP. and E. glauca GREENE the main alkaloidal component is the quaternary base californidine. Eschscholtzine, allocryptopine, and protopine belong among the dominant tertiary alkaloids, which are accompanied by a small amount of N-methyllaurotetanine and the quaternary benzophenanthridines (sanguinarine, chelerythrine, chelirubine, chelilutine, and macarpine). The pavinane alkaloids isonorargemonine, caryachine, norargemonine, and bisnorargemonine and the aporphine alkaloids corydine and isocorydine were isola

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17

Slavík, Jiří, Leonora Slavíková, and Jitka Bochořáková. "Alkaloids from Papaver rhoeas var. chelidonioides O. KUNTZE, P. confine JORD., and P. dubium L." Collection of Czechoslovak Chemical Communications 54, no. 4 (1989): 1118–25. http://dx.doi.org/10.1135/cccc19891118.

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Papaver rhoeas var. chelidonioides O. KUNTZE (diploid, 2n = 14) contains rhoeadine (0.027%) and coptisine (0.004%) as the dominant alkaloids, the latter being the yellow principle of the latex. As minor constituents were isolated protopine, papaverrubine A, rhoeagenine, (-)-stylopine, an unidentified alkaloid PCH 1 (m.p. 205 °C), 2-methyl-1,2,3,4-tetrahydro-β-carboline and (-)-trans-N-methylstylopinium hydroxide. Chromatographic analysis detected isorhoeadine, allocryptopine, cryptopine, papaverrubine C, D and E, scoulerine, isoboldine, berberine, corysamine, magnoflorine and corytuberine. P.

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18

Husna Hasnan, Muhammad Hafiz, Yasodha Sivasothy, Kooi Yeong Khaw, et al. "N-Methyl Costaricine and Costaricine, Two Potent Butyrylcholinesterase Inhibitors from Alseodaphne pendulifolia Gamb." International Journal of Molecular Sciences 24, no. 13 (2023): 10699. http://dx.doi.org/10.3390/ijms241310699.

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Studies have been conducted over the last decade to identify secondary metabolites from plants, in particular those from the class of alkaloids, for the development of new anti-Alzheimer’s disease (AD) drugs. The genus Alseodaphne, comprising a wide range of alkaloids, is a promising source for the discovery of new cholinesterase inhibitors, the first-line treatment for AD. With regard to this, a phytochemical investigation of the dichloromethane extract of the bark of A. pendulifolia Gamb. was conducted. Repeated column chromatography and preparative thin-layer chromatography led to the isola

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19

Marpaung, Jon Kenedy, and Melisa Rekayana Tambuan. "AKTIVITAS PENGHAMBATAN ENZIM PROTEASE 6LU7 VIRUS SARS-COV-2 OLEH SENYAWA ALKALOID DARI ATTARASA (Litsea cubeba (Lour.)Pers.) SECARA IN-SILICO." JURNAL FARMANESIA 7, no. 2 (2020): 1–8. http://dx.doi.org/10.51544/jf.v7i2.2769.

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Attarasa (Litsea cubeba (Lour.) Pers.) is a mountain plant known as "Mountain pepper" or "Mountain Pepper". This plant contains alkaloids, such as Oblongine; Actinodaphine; Isoboldine; Cassameridine; Coclaurine; Corydine; Corytuberine; Dicentrine; Laurotetanine; Lindcarpine; Isocorydine; Isodomesticine; Juziphine; N-Methylcoclaurine; N-Methyllaurotetanine; N-Methyllindcarpine; Norcorydine; Norisoboldine; Norisocorydine; Xanthoplanine. Alkaloids in Attarasa (Litsea cubeba (Lour.) Pers.) have properties such as antimicrobials. This study aimed to determine the inhibition of the protease enzyme 6

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20

Koirala, Pramila, and Bimala Singh. "Dicentra scandens (D.Don) Walp. - A Potential Source of Antimicrobial Agent." International Journal of Toxicological and Pharmacological Research 9, no. 1 (2017): 6–14. https://doi.org/10.5281/zenodo.12730297.

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<em>Dicentra scandens</em> (D.Don) Walp. locally called as ‘<em>Jogi Lahara</em>’ belongs to the Family <em>Fumariaceae</em> and is used in traditional medicine in Sikkim, a North Eastern state of India. The present study investigated the antimicrobial properties of aqueous and methanol extracts of <em>Dicentra scandens</em> (D.Don) Walp. against some test Gram negative and Gram positive bacteria. Using agar well diffusion method, aqueous and methanol extracts of roots of <em>Dicentra scandens </em>were tested against <em>Escherichia</em><em>

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21

Wiseman, Timothy Peter. "Locating Corydon." Hermes 151, no. 3 (2023): 334–45. http://dx.doi.org/10.25162/hermes-2023-0027.

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22

Harrison, S. J. "The lark ascending: Corydon, Corydon (Vergil, Ecl. 7.70)." Classical Quarterly 48, no. 1 (1998): 310–11. http://dx.doi.org/10.1093/cq/48.1.310.

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23

Ribár, B., D. Lazar, P. Radivojević, P. Engel, O. Gašić, and I. Kanyó. "Structure of corydaline." Acta Crystallographica Section C Crystal Structure Communications 48, no. 10 (1992): 1864–66. http://dx.doi.org/10.1107/s0108270192001951.

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24

BOHN, HORST. "The spine armament of the legs as an important means for the characterisation of the genera of Corydiinae and their relationships (Blattodea, Corydiidae)." Zootaxa 5482, no. 1 (2024): 1–79. http://dx.doi.org/10.11646/zootaxa.5482.1.1.

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The Palaearctic species of Corydiinae having no apical spine on the femora of the frontleg (48 species distributed to the genera Heterogamisca, Heterogamodes, Hemelytroblatta, Leiopteroblatta, Mononychoblatta, Nymphrytria, Psammoblatta) were studied in mainly three characters: tibia armament, features of the right phallomere, and distribution of bristles on the subgenital plate. The results suggest considerable changes in the classification with now 5 genera and several subgenera: (1) Heterogamodes with subgenera Heterogamodes, Heterogamisca, and Atuberculoblatta subgen. nov.; (2) Hemelytrobla

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25

Weingardt, Richard G. "Corydon Tyler Purdy." Leadership and Management in Engineering 10, no. 3 (2010): 124–30. http://dx.doi.org/10.1061/(asce)lm.1943-5630.0000067.

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26

Rueffer, Martina, Wolfgang Bauer, and Meinhart H. Zenk. "The formation of corydaline and related alkaloids in Corydalis cava in vivo and in vitro." Canadian Journal of Chemistry 72, no. 1 (1994): 170–75. http://dx.doi.org/10.1139/v94-026.

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The biosynthesis of corydaline and thalictricavine has been investigated by application of [8-3H]-labelled palmatine and berberine to Corydalis cava bulb tissue. In both cases, high incorporation into the respective (14R,13S)corydaline and -thalictricavine was observed. (S)-[14-3H, 8-14C]Scoulerine was also transferred into corydaline with all of the tritium being lost, indicating that a redox reaction had taken place in the transition of the (14S) to the (14R) product. A partly enriched protein fraction catalyzed the reduction of both protoberberine precursors to the 7,8-dihydro intermediate,

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27

RIBAR, B., D. LAZAR, P. RADIVOJEVIC, P. ENGEL, O. GASIC, and I. KANYO. "ChemInform Abstract: Structure of Corydaline." ChemInform 24, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.199305278.

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28

Adeniran, Olawole Yakubu. "Identification of Novel Plant-derived Inhibitors of the EGFR Kinase Domain Using vHTS, QSAR and Molecular Docking Approaches." Asian Journal of Biochemistry, Genetics and Molecular Biology 16, no. 7 (2024): 69–84. http://dx.doi.org/10.9734/ajbgmb/2024/v16i7392.

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The epidermal growth factor receptor (EGFR) protein tyrosine kinase (PTK) is a crucial target in the pursuit of anti-tumor drug discovery. This study investigates 305 phytochemicals from five known anticancer plants (Anacardium occidentale, Annona muricata, Spondias mombin, Ocimum gratisimum, and Zingiber officinale) for their potential as EGFR kinase domain inhibitors. Through Virtual High Throughput Screening (vHTS), lead compounds were identified and subjected to ADMET filtering. A Quantitative Structure-Activity Relationship (QSAR) model was developed using bioassay data from the ChEMBL da

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29

Qiu, Lu, Yang-Li Che, and Zong-Qing Wang. "A taxonomic study of Eupolyphaga Chopard, 1929 (Blattodea: Corydiidae: Corydiinae)." Zootaxa 4506, no. 1 (2018): 1–68. https://doi.org/10.11646/zootaxa.4506.1.1.

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30

Slavík, Jiří, and Leonora Slavíková. "Alkaloids from Corydalis nobilis (L.) PERS. and C. intermedia (L.) MÉRAT." Collection of Czechoslovak Chemical Communications 54, no. 7 (1989): 2009–20. http://dx.doi.org/10.1135/cccc19892009.

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Rhizomes of Corydalis nobilis (L.) PERS. (3% of alkaloids) contain (+)-tetrahydropalmatine, (+)-bicuculline and (+)-corytuberine as the main constituents of the tertiary alkaloid fraction. Protopine, (+)-corypalmine and (+)-stylopine, which also belong to the dominant alkaloids, were isolated in lesser amounts. As minor alkaloids were isolated (±)-tetrahydropalmatine, (+)-corydaline, allocryptopine, cryptopine, (-)-scoulerine, (+)-adlumidine, (+)-sinactine, (±)-corlumine, isoboldine, (+)-corybulbine, (±)-stylopine and (-)-isocorypalmine. The fraction of quaternary protoberberine alkaloids affo

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31

Qiu, Lu, Yan-Li Che, and Zong-Qing Wang. "Contributions to some Corydiinae genera (Blattodea: Corydioidea: Corydiidae) from China." Journal of Natural History 52, no. 21-22 (2018): 1433–61. https://doi.org/10.1080/00222933.2018.1463406.

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Qiu, Lu, Che, Yan-Li, Wang, Zong-Qing (2018): Contributions to some Corydiinae genera (Blattodea: Corydioidea: Corydiidae) from China. Journal of Natural History (J. Nat. Hist.) 52 (21-22): 1433-1461, DOI: 10.1080/00222933.2018.1463406, URL: http://dx.doi.org/10.1080/00222933.2018.1463406

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32

Qiu, Lu, Yanli Che, and Zongqing Wang. "Revision of Eucorydia Hebard, 1929 from China, with notes on the genus and species worldwide (Blattodea, Corydioidea, Corydiidae)." ZooKeys 709 (October 18, 2017): 17–56. https://doi.org/10.3897/zookeys.709.14755.

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The cockroach genus Eucorydia from China is revised. Five new species are described and illustrated: Eucorydia linglong sp. n., Eucorydia pilosa sp. n., Eucorydia splendida sp. n., Eucorydia guilinensis sp. n., and Eucorydia tangi sp. n.. Corydia purpuralis Kirby, 1903 and Eucorydia paucipilosa Woo, Guo & Feng, 1986 are confirmed to be junior synonyms of Eucorydia dasytoides (Walker, 1868). Eucorydia hilaris (Kirby, 1903) is newly recorded from China. This genus and currently known species from around the world are discussed. The status of Eucorydia maxwelli (Hanitsch, 1915) is revived. Co

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33

Bohn, Horst. "The spine armament of the legs as an important means for the characterisation of the genera of Corydiinae and their relationships (Blattodea, Corydiidae)." Zootaxa 5482, no. 1 (2024): 1–79. https://doi.org/10.11646/zootaxa.5482.1.1.

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Bohn, Horst (2024): The spine armament of the legs as an important means for the characterisation of the genera of Corydiinae and their relationships (Blattodea, Corydiidae). Zootaxa 5482 (1): 1-79, DOI: 10.11646/zootaxa.5482.1.1, URL: http://dx.doi.org/10.11646/zootaxa.5482.1.1

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34

Tang, Hsin-Chieh, and Calvin Yu-Chian Chen. "Drug Design of Cyclin-Dependent Kinase 2 Inhibitor for Melanoma from Traditional Chinese Medicine." BioMed Research International 2014 (2014): 1–17. http://dx.doi.org/10.1155/2014/798742.

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One has found an important cell cycle controller. This guard can decide the cell cycle toward proliferation or quiescence. Cyclin-dependent kinase 2 (CDK2) is a unique target among the CDK family in melanoma therapy. We attempted to find out TCM compounds from TCM Database@Taiwan that have the ability to inhibit the activity of CDK2 by systems biology. We selected Tetrahydropalmatine, Reserpiline, and (+)-Corydaline as the candidates by docking and screening results for further survey. We utilized support vector machine (SVM), multiple linear regression (MLR) models and Bayesian network for va

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35

Qiu, Lu, Zong-Qing Wang, and Yan-Li Che. "Minpolyphaga inexpectata, a new genus and species of Polyphagini (Blattodea: Corydiidae: Corydiinae) from southeast China." Acta Entomologica Musei Nationalis Pragae 59, no. 2 (2019): 513–18. https://doi.org/10.2478/aemnp-2019-0042.

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Qiu, Lu, Wang, Zong-Qing, Che, Yan-Li (2019): Minpolyphaga inexpectata, a new genus and species of Polyphagini (Blattodea: Corydiidae: Corydiinae) from southeast China. Acta Entomologica Musei Nationalis Pragae 59 (2): 513-518, DOI: 10.2478/aemnp-2019-0042, URL: http://dx.doi.org/10.2478/aemnp-2019-0042

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Jung, Ji Won, Mi Ran Choi, Yong Sam Kwon, Jin Seok Jeong, Miwon Son, and Hee Eun Kang. "Gender differences in corydaline pharmacokinetics in rats." Xenobiotica 45, no. 5 (2014): 456–63. http://dx.doi.org/10.3109/00498254.2014.988772.

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Codazzi, Paola. "Alain Goulet, Les “Corydon” d’André Gide." Studi Francesi, no. 175 (LIX | I) (April 1, 2015): 189. http://dx.doi.org/10.4000/studifrancesi.590.

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Eckerman, Chris. "THYRSIS’ ARCADIAN SHEPHERDS IN VIRGIL'S SEVENTH ECLOGUE." Classical Quarterly 65, no. 2 (2015): 669–72. http://dx.doi.org/10.1017/s0009838815000142.

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In Virgil's seventh Eclogue, Meliboeus relates a singing contest that Corydon and Thyrsis undertook. Upon beginning their songs, Corydon invokes the Libethrian nymphs (21), and Thyrsis invokes ‘Arcadian shepherds’ (25–6). Scholars have previously interpreted Thyrsis’ Arcadian shepherds as people, but here I suggest that they should be interpreted as divinities. In support of this assertion, I rely on the expectations of the capping style (which requires that Thyrsis ‘cap’ Corydon's invocation of Libethrian nymphs), Virgil's description of the setting and the characters present, an epigram by E

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Spisak, April. "Corydon & the Island of Monsters (review)." Bulletin of the Center for Children's Books 59, no. 7 (2006): 309. http://dx.doi.org/10.1353/bcc.2006.0195.

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Seropian, Armen, Eka Arsenashvili, Natalia Bulbulashvili, et al. "The first DNA-assisted record of Hemelytroblatta livida (Blattodea: Corydiidae) from Georgia with notes on Corydiinae species composition in the Caucasus." Caucasiana 2 (May 2, 2023): 71–75. http://dx.doi.org/10.3897/caucasiana.2.e103189.

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The fossorial sand cockroach Hemelytroblatta livida (Brunner von Wattenwyl, 1865) is reported from Georgia for the first time, with a commentary on the species composition of the Corydiinae Saussure, 1864 subfamily in the Caucasus. Collection data, pictures of the male and female, and DNA barcodes are also provided. Furthermore, information on Polyphaga aegyptiaca (Linnaeus, 1758) is provided, along with images of the male, female, and juvenile.

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Seropian, Armen, Eka Arsenashvili, Natalia Bulbulashvili, et al. "The first DNA-assisted record of Hemelytroblatta livida (Blattodea: Corydiidae) from Georgia with notes on Corydiinae species composition in the Caucasus." Caucasiana 2 (May 2, 2023): 71–75. https://doi.org/10.3897/caucasiana.2.e103189.

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The fossorial sand cockroach Hemelytroblatta livida (Brunner von Wattenwyl, 1865) is reported from Georgia for the first time, with a commentary on the species composition of the Corydiinae Saussure, 1864 subfamily in the Caucasus. Collection data, pictures of the male and female, and DNA barcodes are also provided. Furthermore, information on Polyphaga aegyptiaca (Linnaeus, 1758) is provided, along with images of the male, female, and juvenile.

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Wu, Lehao, Weiyue Zhang, Xin Qiu, et al. "Identification of Alkaloids from Corydalis yanhusuo W. T. Wang as Dopamine D1 Receptor Antagonists by Using CRE-Luciferase Reporter Gene Assay." Molecules 23, no. 10 (2018): 2585. http://dx.doi.org/10.3390/molecules23102585.

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Corydalis yanhusuo W. T. Wang (C. yanhusuo) has been traditionally used for drug addiction and pain relief in China. In our previous study, we showed that the extract of C. yanhusuo blocks dopamine receptors, demonstrating that its pharmacological activities are mostly due to the antagonistic effects of some of its components at dopamine receptors. As part of our ongoing project on C. yanhusuo, the aim of the present study is to establish a high-throughput and low-cost screening assay system and test the abilities of the isolated alkaloids from C. yanhusuo to inhibit dopamine-induced dopamine

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Hawcroft, Michael. "Gide's Corydon, ‘mise en abyme’, and Autobiographical Fiction." Nottingham French Studies 33, no. 2 (1994): 47–54. http://dx.doi.org/10.3366/nfs.1994-2.006.

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QIU, LU, YANG-LI CHE, and ZONG-QING WANG. "A taxonomic study of Eupolyphaga Chopard, 1929 (Blattodea: Corydiidae: Corydiinae)." Zootaxa 4506, no. 1 (2018): 1. http://dx.doi.org/10.11646/zootaxa.4506.1.1.

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The cockroach genus Eupolyphaga is revised. Twenty species and two subspecies are recognized, with thirteen species and two subspecies are new to science: E. daweishana sp. nov., E. dongi sp. nov., E. fengi sp. nov., E. hanae sp. nov., E. hupingensis sp. nov., E. maculata sp. nov., E. nigrifera sp. nov., E. nigrinotum sp. nov., E. pilosa sp. nov., E. robusta sp. nov., E. shennongensis sp. nov., E. wooi sp. nov., E. xuorum sp. nov., E. everestiana reni subsp. nov., and E. fengi yongshengensis subsp. nov. Homœogamia sinensis Saussure is placed as a junior synonym of E. sinensis (Walker) and the

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Wang, Hui-Qiang, Jin Hu, Hai-Yan Yan, Shuo Wu, and Yu-Huan Li. "Corydaline inhibits enterovirus 71 replication by regulating COX-2 expression." Journal of Asian Natural Products Research 19, no. 11 (2017): 1124–33. http://dx.doi.org/10.1080/10286020.2017.1386658.

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Qiu, Lu, Yan-Li Che, and Zong-Qing Wang. "Contributions to some Corydiinae genera (Blattodea: Corydioidea: Corydiidae) from China." Journal of Natural History 52, no. 21-22 (2018): 1433–61. http://dx.doi.org/10.1080/00222933.2018.1463406.

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Guo, Pengcheng, Qizheng Wang, Xiaoqiang Xiang, et al. "Establishment of Dissolution Test Method for Multi-Components in Traditional Chinese Medicine Preparations Based on In Vitro–In Vivo Correlation." Pharmaceuticals 17, no. 8 (2024): 1065. http://dx.doi.org/10.3390/ph17081065.

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In this study, a multi-component integrated dissolution evaluation system of Yuanhu Zhitong tablets (YZTs) was established based on in vitro and in vivo correlation (IVIVC). The dissolution tests of five quality markers (Q-markers), including tetrahydropalmatine, α-allocryptopine, protopine, corydaline, and byakangelicin, in YZTs were conducted under different dissolution conditions, and pharmacokinetic studies were performed in beagle dogs to construct a correlation model using numerical deconvolution. The data of the five ingredients were integrated in vitro and in vivo according to the biop

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Cairns, Lucille. "Gide's "Corydon": The Politics of Sexuality and Sexual Politics." Modern Language Review 91, no. 3 (1996): 582. http://dx.doi.org/10.2307/3734086.

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Luo, Tian, Xuemei Deng, Zhao Li, Dan Liu, Huaixiu Wen, and Zhen Wang. "Synthesis and anti-hepatocellular carcinoma effects of corydamine from Hypecoum Leptocarpum." Phytochemistry Letters 51 (October 2022): 119–26. http://dx.doi.org/10.1016/j.phytol.2022.08.006.

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Selvaraj, Baskar, Dae Won Kim, Ki-Yeon Yoo, et al. "Neuroprotective mechanism of corydaline in glutamate-induced neurotoxicity in HT22 cells." International Journal of Oral Biology 49, no. 1 (2024): 10–17. http://dx.doi.org/10.11620/ijob.2024.49.1.10.

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