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Journal articles on the topic 'Lysergol'

Author: Grafiati

Published: 24 April 2022

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1

Merkel, Stefan, Robert Köppen, Matthias Koch, Franziska Emmerling, and Irene Nehls. "Lysergol monohydrate." Acta Crystallographica Section E Structure Reports Online 68, no. 2 (2012): o523. http://dx.doi.org/10.1107/s1600536812002632.

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2

Patil, Shrikant, Manish Nivsarkar, and Sheetal Anandajiwala. "Isolation and TLC Densitometric Quantification of Lysergol from the Seeds of Ipomoea muricata (Linn.) Jacq." ISRN Chromatography 2013 (January 22, 2013): 1–6. http://dx.doi.org/10.1155/2013/134586.

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Seeds of Ipomoea muricata, well known in Ayurveda for its purgative action, contains mainly indole alkaloids. Lysergol (major alkaloid) exhibits hypotensive, psychotropic, and uterus and intestine-stimulating properties. TLC fingerprint profile of I. muricata seeds was developed using chloroform : methanol (95 : 5 v/v) as the mobile phase. Plate was visualized under UV 254 nm and UV 366 nm and after derivatization with Van Urk reagent. Lysergol resolved at . Further, TLC-densitometric method was developed and validated for quantification of Lysergol avoiding derivatization step. Ethyl acetate

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3

Harris, J. R., and D. C. Horwellt. "Conversion of Agroclavine to Lysergol." Synthetic Communications 22, no. 7 (1992): 995–99. http://dx.doi.org/10.1080/00397919208019288.

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4

Shukla, M., M. Y. Malik, S. Jaiswal, et al. "A mechanistic investigation of the bioavailability enhancing potential of lysergol, a novel bioenhancer, using curcumin." RSC Advances 6, no. 64 (2016): 58933–42. http://dx.doi.org/10.1039/c6ra09307h.

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5

Stevenson, David E., Vladimír Křen, Petr Halada та Petr Sedmera. "Enzymatic Preparation of Lysergol β-D-Glucuronide". Collection of Czechoslovak Chemical Communications 65, № 1 (2000): 117–21. http://dx.doi.org/10.1135/cccc20000117.

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6

Křen, Vladimír, and Petr Sedmera. "N-1-Trimethylsilyl Derivatives of Ergot Alkaloids." Collection of Czechoslovak Chemical Communications 61, no. 8 (1996): 1248–53. http://dx.doi.org/10.1135/cccc19961248.

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N-1-Trimethylsilyl derivatives of five different suitably protected parent ergot (clavine) alkaloids (agroclavine 1a, elymoclavine 2a, lysergol 3a, lysergene 4a, and 9,10-dihydrolysergol 5a) were prepared in 47-94% yields by refluxing the (protected) parent compounds with N-methyl-N-(trimethylsilyl)trifluoroacetamide in acetonitrile under nitrogen atmosphere.

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7

Patil, Shrikant, Ranjeet Prasad Dash, Sheetal Anandjiwala, and Manish Nivsarkar. "Simultaneous quantification of berberine and lysergol by HPLC-UV: evidence that lysergol enhances the oral bioavailability of berberine in rats." Biomedical Chromatography 26, no. 10 (2011): 1170–75. http://dx.doi.org/10.1002/bmc.2674.

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8

Stevenson, David E., Vladimir Kren, Petr Halada та Petr Sedmera. "ChemInform Abstract: Enzymatic Preparation of Lysergol β-D-Glucuronide." ChemInform 31, № 17 (2010): no. http://dx.doi.org/10.1002/chin.200017214.

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9

Inuki, Shinsuke, Shinya Oishi, Nobutaka Fujii, and Hiroaki Ohno. "Total Synthesis of (±)-Lysergic Acid, Lysergol, and Isolysergol by Palladium-Catalyzed Domino Cyclization of Amino Allenes Bearing a Bromoindolyl Group." Organic Letters 13, no. 8 (2011): 2145. http://dx.doi.org/10.1021/ol200375v.

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10

Inuki, Shinsuke, Shinya Oishi, Nobutaka Fujii, and Hiroaki Ohno. "Total Synthesis of (±)-Lysergic Acid, Lysergol, and Isolysergol by Palladium-Catalyzed Domino Cyclization of Amino Allenes Bearing a Bromoindolyl Group." Organic Letters 10, no. 22 (2008): 5239–42. http://dx.doi.org/10.1021/ol8022648.

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11

Yuan, Haosen, Zhixian Guo, and Tuoping Luo. "Synthesis of (+)-Lysergol and Its Analogues To Assess Serotonin Receptor Activity." Organic Letters 19, no. 3 (2017): 624–27. http://dx.doi.org/10.1021/acs.orglett.6b03779.

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12

Inuki, Shinsuke, Akira Iwata, Shinya Oishi, Nobutaka Fujii, and Hiroaki Ohno. "Enantioselective Total Synthesis of (+)-Lysergic Acid, (+)-Lysergol, and (+)-Isolysergol by Palladium-Catalyzed Domino Cyclization of Allenes Bearing Amino and Bromoindolyl Groups." Journal of Organic Chemistry 76, no. 7 (2011): 2072–83. http://dx.doi.org/10.1021/jo102388e.

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13

Ninomiya, Ichiya, Toshiko Kiguchi, and Chiyomi Hashimoto. "A Total Synthesis of (±)-Lysergol, a 9-Ergolene Type of Ergot Alkaloi." HETEROCYCLES 23, no. 6 (1985): 1377. http://dx.doi.org/10.3987/r-1985-06-1377.

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14

Hill, N. S. "Affinity of Anti‐lysergol and Anti‐Ergonovine Monoclonal Antibodies to Ergot Alkaloid Derivatives." Crop Science 37, no. 2 (1997): 535–37. http://dx.doi.org/10.2135/cropsci1997.0011183x003700020037x.

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15

Milde, Bastian, Martin Pawliczek, Peter G. Jones, and Daniel B. Werz. "Enantioselective Total Synthesis of (+)-Lysergol: A Formalanti-Carbopalladation/Heck Cascade as the Key Step." Organic Letters 19, no. 7 (2017): 1914–17. http://dx.doi.org/10.1021/acs.orglett.7b00675.

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16

Patil, Shrikant, Ranjeet Prasad Dash, Sheetal Anandjiwala, and Manish Nivsarkar. "PHARMACOKINETIC STUDY OF BERBERINE FROM RASONT AND IMPLICATION OF LYSERGOL FOR ITS BIOAVAILABILITY ENHANCEMENT." Journal of Liquid Chromatography & Related Technologies 36, no. 3 (2013): 336–48. http://dx.doi.org/10.1080/10826076.2012.657731.

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17

Rohilla, Mehak, Neetu Goel, Tej Vir Singh, P. Venugopalan, N. V. Suresh Kumar, and K. Tewari. "Theoretical and experimental studies on solubility and reactivity behavior of lysergol, elymoclavine, and dihydrolysergol." International Journal of Quantum Chemistry 113, no. 10 (2012): 1427–35. http://dx.doi.org/10.1002/qua.24335.

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18

Maurya, Anupam, Gaurav R. Dwivedi, Mahendra P. Darokar, and Santosh K. Srivastava. "Antibacterial and Synergy of Clavine Alkaloid Lysergol and its Derivatives Against Nalidixic Acid-ResistantEscherichia coli." Chemical Biology & Drug Design 81, no. 4 (2013): 484–90. http://dx.doi.org/10.1111/cbdd.12103.

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19

Bhunia, Subhajit, Saikat Chaudhuri, and Alakesh Bisai. "Total Syntheses of Pyroclavine, Festuclavine, Lysergol, and Isolysergol via a Catalytic Asymmetric Nitro-Michael Reaction." Chemistry - A European Journal 23, no. 47 (2017): 11234–38. http://dx.doi.org/10.1002/chem.201702459.

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20

Smirnov, Viktor Mihajlovich, Dmitrij Sergeevich Sveshnikov, Igor Leonidovich Myasnikov, Tat'jana Evgen'evna Kuznecova, and Jurij Nikolaevich Samko. "Evidences of Existence of Serotoninergic Nerves, Enhancing Duodenal Motility." Annals of the Russian academy of medical sciences 70, no. 6 (2015): 718–26. http://dx.doi.org/10.15690/vramn570.

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The review is devoted to the mechanism of duodenal motility activation caused by sympathetic nerves. The authors have found that stimulation of the sympathetic trunk in the thoracic cavity in dogs in most cases provide not inhibitory but excitatory motor responses of the duodenum. Excitatory effects were eliminated during 5HT-receptors blockade by promedol and lysergol. Analysis of publications showed that sympathetic trunk contains serotoninergic fibers, providing excitatory motor responses of the duodenum to electrical nerve stimulation. According to histochemical and physiological studies,

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21

Klotz, James L., Hannah Stokley, Huihua Ji, Nabanita Chattopadhyay, and David L. Harmon. "PSII-24 Assessment of the contractility of bovine lateral saphenous and digital veins in response to ergot alkaloids." Journal of Animal Science 98, Supplement_4 (2020): 375. http://dx.doi.org/10.1093/jas/skaa278.659.

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Abstract Decreased blood flow caused by vasoconstriction is a hallmark of ergot alkaloid exposure. Previous research has utilized the cranial branch of the lateral saphenous vein as a model to characterize the impact of ergot alkaloids on bovine peripheral vasculature. The digital vein is more distal and closer to the hoof where damage caused by vasoconstriction occurs and may be more sensitive to ergot alkaloids. Thus, the objective was to compare contractility of the bovine lateral saphenous vein and the digital vein to increasing concentrations of ergot alkaloids. Blood vessels were collect

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22

Schitter, Theresa, Andreas Reding, and Daniel B. Werz. "Cascades Involving anti-Carbopalladation Steps: From Our Initial Hypothesis to Natural Product Synthesis." Synlett 30, no. 11 (2019): 1275–88. http://dx.doi.org/10.1055/s-0037-1612257.

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Our endeavors in the design, realization and application of a formal anti-carbopalladation of alkynes are summarized. Whereas numerous examples of syn-carbopalladation steps embedded in cascade reactions are known, there have been almost no examples of the corresponding anti-carbopalladation steps. From a personal perspective, this account provides insights on the original considerations and hypotheses, and their validation or invalidation by experimental and computational means. This account also aims at clarifying how different ideas have been developed and how novel reaction sequences pavin

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23

Javed, Shamama, Kanchan Kohli, and Mushir Ali. "FORCED DEGRADATION AND PH STABILITY STUDIES OF LYSERGOL: AN ERGOLIC ALKALOID BY STABILITY INDICATING RP HPLC-UV METHOD." Journal of Liquid Chromatography & Related Technologies 35, no. 4 (2012): 471–83. http://dx.doi.org/10.1080/10826076.2011.601498.

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24

Maurya, Anupam, Ram Kishore Verma, and Santosh Kumar Srivastava. "Quantitative determination of bioactive alkaloids lysergol and chanoclavine in Ipomoea muricata by reversed-phase high-performance liquid chromatography." Biomedical Chromatography 26, no. 9 (2011): 1096–100. http://dx.doi.org/10.1002/bmc.1753.

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25

Bacelar, Rafael Gomes Abreu, Márcio dos Santos Rocha, João Farias Sousa Junior, et al. "Analysis of aflatoxins and ergot alkaloids in feeds for adult equine." Research, Society and Development 10, no. 11 (2021): e539101119697. http://dx.doi.org/10.33448/rsd-v10i11.19697.

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Mycotoxins are products resulting from fungi metabolism normally present in the environment and which can develop in food. The aim of this study was the fungi quantification, aflatoxin detection and investigation of ergot alkaloids occurrence in pelleted feed for adult equines during storage. The feed samples were collected from three rural properties with equideoculture activity in the city of Teresina, Piauí, Brazil. The results showed that was no significant difference (p<0.05) for the counting of colony-forming units (CFU/g) of filamentous fungi and yeasts in the samples. Aflatoxins B1,

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26

Javed, Shamama, Kanchan Kohli, and Mushir Ali. "Application of Response Surface Methodology to Microwave-Assisted Extraction of Lysergol from Ipomoea Genus and Its Characterization by RP HPLC-UV." Journal of Pharmaceutical Innovation 6, no. 2 (2011): 88–96. http://dx.doi.org/10.1007/s12247-011-9106-6.

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27

NINOMIYA, ICHIYA, CHIYOMI HASHIMOTO, TOSHIKO KIGUCHI, and TAKEAKI NAITO. "Photocyclization of enamides. XXV Syntheses of despyrrole analogues of ergot alkaloids including elymoclavine, lysergol, isolysergol, lysergine, isolysergine, fumigaclavine, agroclavine, and lysergene." CHEMICAL & PHARMACEUTICAL BULLETIN 34, no. 7 (1986): 2799–809. http://dx.doi.org/10.1248/cpb.34.2799.

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28

PERTZ, HEINZ H., ANTHONY M. BROWN, TRACEY L. GAGER та ALBERTO J. KAUMANN. "Simple O-Acylated Derivatives of Lysergol and Dihydrolysergol-I: Synthesis and Interaction with 5-HT2A, 5-HT2Cand 5-HT1BReceptors, and α1Adrenergic Receptors". Journal of Pharmacy and Pharmacology 51, № 3 (1999): 319–30. http://dx.doi.org/10.1211/0022357991772321.

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29

Duringer, J. M., M. J. M. Delorme, A. Lehner, and A. M. Craig. "A review of the ergot alkaloids found in endophyte-infected tall fescue and perennial ryegrass and their metabolism after ingestion by livestock." NZGA: Research and Practice Series 13 (January 1, 2007): 377–82. http://dx.doi.org/10.33584/rps.13.2006.3162.

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Tall fescue (Festuca arundinacea) and perennial ryegrass (Lolium perenne) are perennial cool-season grasses which are infected with the endophytic fungi, Neotyphodium coenophialum and N. lolii, respectively. These endophytes have been increasingly selected for, as they confer benefits such as pest resistance and drought tolerance to the plant. However, livestock grazing endophyte-infected (E+) grasses are negatively impacted by fungal ergot and lolitrem alkaloids, which are responsible for a variety of mammalian diseases including fescue toxicosis (summer syndrome, fescue foot and fat necrosis

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30

Reed, K. F. M., J. L. Vaughan, L. J. Cummins, and D. D. Moore. "Impact of mycotoxins and of a mycotoxin deactivator on alpacas grazing perennial ryegrass infected with wild endophyte (Neotyphodium spp.)." Animal Production Science 50, no. 9 (2010): 902. http://dx.doi.org/10.1071/an10068.

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Liveweight gain, animal health and the effectiveness of a mycotoxin deactivator were studied on an old pasture that contained 61% perennial ryegrass. Sixty-seven percent of the ryegrass population was infected with endophyte (Neotyphodium spp.). The pasture was fenced into two halves and two groups of 28 alpaca male weaners were rotated between the two plots. Nine to 10 Suris and 18–19 Huacayas were allocated to each group. One group was fed a concentrate supplement (100 g/head per day) and the other was fed the same supplement to which was added the toxin deactivator, Mycofix® Plus (5 g/100 g

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31

Gooneratne, SR, M. Scannell, M. Wellby, and L. Fletcher. "Changes in concentrations of lysergol in urine and prolactin in plasma, rectal temperature and respiration rate in sheep selected for resistance or susceptibility to ryegrass staggers and fed ergovaline." New Zealand Veterinary Journal 59, no. 5 (2011): 233–38. http://dx.doi.org/10.1080/00480169.2011.601538.

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32

Chen, Xue-Dong, Navneet Kaur, David R. Horton, W. Rodney Cooper, Jawwad A. Qureshi, and Lukasz L. Stelinski. "Crude Extracts and Alkaloids Derived from Ipomoea-Periglandula Symbiotic Association Cause Mortality of Asian Citrus Psyllid Diaphorina citri Kuwayama (Hemiptera: Psyllidae)." Insects 12, no. 10 (2021): 929. http://dx.doi.org/10.3390/insects12100929.

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Asian citrus psyllid Diaphorina citri Kuwayama (Hemiptera: Psyllidae) is an important economic pest of citrus crops because it vectors the causal pathogen of huanglongbing (HLB; aka citrus greening). Population suppression of D. citri with insecticides has been disproportionally relied on for HLB management and a greater diversity of more sustainable tools is needed. Periglandula spp. is a fungal endosymbiont (family Clavicipitaceae) that forms a mutualistic relationship with members of plants in family Convolvulaceae. This association results in the production of ergot alkaloids that were pre

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33

Pertz, Heinz H., H. Christian Milhahn, and Eckart Eich. "Cycloalkanecarboxylic Esters Derived from Lysergol, Dihydrolysergol-I, and Elymoclavine as Partial Agonists and Antagonists at Rat 5-HT2AReceptors: Pharmacological Evidence that the Indolo[4,3-fg]quinoline System of the Ergolines Is Responsible for High 5-HT2AReceptor Affinity." Journal of Medicinal Chemistry 42, no. 4 (1999): 659–68. http://dx.doi.org/10.1021/jm981092u.

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34

Keller, Ullrich, Mehmet Han, and Marina Stoeffler-Meilicke. "D-Lysergic acid activation and cell-free synthesis of D-lysergyl peptides in an enzyme fraction from the ergot fungus Claviceps purpurea." Biochemistry 27, no. 16 (1988): 6164–70. http://dx.doi.org/10.1021/bi00416a051.

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35

Robinson, Sarah L., and Daniel G. Panaccione. "Heterologous Expression of Lysergic Acid and Novel Ergot Alkaloids in Aspergillus fumigatus." Applied and Environmental Microbiology 80, no. 20 (2014): 6465–72. http://dx.doi.org/10.1128/aem.02137-14.

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ABSTRACTDifferent lineages of fungi produce distinct classes of ergot alkaloids. Lysergic acid-derived ergot alkaloids produced by fungi in the Clavicipitaceae are particularly important in agriculture and medicine. The pathway to lysergic acid is partly elucidated, but the gene encoding the enzyme that oxidizes the intermediate agroclavine is unknown. We investigated two candidate agroclavine oxidase genes from the fungusEpichloë festucaevar.lolii×Epichloë typhinaisolate Lp1 (henceforth referred to asEpichloësp. Lp1), which produces lysergic acid-derived ergot alkaloids. Candidate geneseasHan

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36

Suryaningsih, Chatarina, and Soleha Hendarsyah. "Pengalaman Anak Jalanan Usia Remaja Dalam Perilaku Inhalasi Lysergic Acid Diethylamide." Jurnal Ilmu Keperawatan Anak 2, no. 2 (2019): 40. http://dx.doi.org/10.32584/jika.v0i0.345.

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Seorang anak bisa menjadi anak jalanan tentu mempunyai hal yang melatarbelakangi dalam kehidupannya. Sehingga anak jalanan sangat rentan untuk terjerumus kedalam perilaku menyimpang salah satunya adalah perilaku inhalasi zat adiktif seperti Lysergic Acid Diethylamide (LSD). Tujuan penelitian ini untuk mengeksplorasi dan menggambarkan pengalaman anak jalanan usia remaja dalam perilaku inhalasi LSD. Jenis penelitian ini adalah penelitian kualitatif dengan pendekatan fenomenologi deskriptif untuk menggambarkan pengalaman anak jalanan usia remaja dalam perilaku inhalasi LSD. Empat partisipan terpi

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37

Moldvai, István, Luca Russo, Kari Rissanen, et al. "Dimerization of (+)-Lysergic Acid Esters." HETEROCYCLES 71, no. 5 (2007): 1075. http://dx.doi.org/10.3987/com-07-11011.

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38

Liu, Qiang, and Yanxing Jia. "Total Synthesis of (+)-Lysergic Acid." Organic Letters 13, no. 18 (2011): 4810–13. http://dx.doi.org/10.1021/ol2018467.

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39

Kanno, Rentaro, Satoshi Yokoshima, Motomu Kanai, and Tohru Fukuyama. "Total synthesis of (+)-lysergic acid." Journal of Antibiotics 71, no. 2 (2017): 240–47. http://dx.doi.org/10.1038/ja.2017.80.

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40

Umezaki, Satoshi, Satoshi Yokoshima, and Tohru Fukuyama. "Total Synthesis of Lysergic Acid." Organic Letters 15, no. 16 (2013): 4230–33. http://dx.doi.org/10.1021/ol4019562.

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41

Zetterberg, Gösta. "Lysergic acid diethylamide and mutation." Hereditas 62, no. 1-2 (2009): 262–64. http://dx.doi.org/10.1111/j.1601-5223.1969.tb02234.x.

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42

Liu, Qiang, Yu-An Zhang, Ping Xu, and Yanxing Jia. "Total Synthesis of (+)-Lysergic Acid." Journal of Organic Chemistry 78, no. 21 (2013): 10885–93. http://dx.doi.org/10.1021/jo4018777.

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43

Riederer, Brigitte, Mehmet Han, and Ullrich Keller. "D-Lysergyl Peptide Synthetase from the Ergot FungusClaviceps purpurea." Journal of Biological Chemistry 271, no. 44 (1996): 27524–30. http://dx.doi.org/10.1074/jbc.271.44.27524.

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44

Tsochatzis, Emmanouil, Joao Alberto Lopes, Fabiano Reniero, Margaret Holland, Jenny Åberg, and Claude Guillou. "Identification of 1-Butyl-Lysergic Acid Diethylamide (1B-LSD) in Seized Blotter Paper Using an Integrated Workflow of Analytical Techniques and Chemo-Informatics." Molecules 25, no. 3 (2020): 712. http://dx.doi.org/10.3390/molecules25030712.

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The rapid dispersion of new psychoactive substances (NPS) presents challenges to customs services and analytical laboratories, which are involved in their detection and characterization. When the seized material is limited in quantity or of a complex nature, or when the target substance is present in very small amounts, the need to use advanced analytical techniques, efficient workflows and chemo-informatics tools is essential for the complete identification and elucidation of these substances. The current work describes the application of such a workflow in the analysis of a single blotter pa

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45

Deruiter, Jack, F. Taylor Noggle, and C. Randall Clark. "Reversed Phase Liquid Chromatographic Separation of Lysergic Acid Diethylamide (LSD) and Lysergic Acid Methylpropylamide (LAMPA)." Journal of Liquid Chromatography 10, no. 15 (1987): 3481–88. http://dx.doi.org/10.1080/01483918708081885.

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46

Penington, N. J., and R. J. Reiffenstein. "Lack of effect of antagonists on serotonin-induced inhibition in rat hippocampus." Canadian Journal of Physiology and Pharmacology 64, no. 11 (1986): 1413–18. http://dx.doi.org/10.1139/y86-239.

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Four putative central nervous system 5-hydroxytryptamine antagonists, methysergide, cyproheptadine, metergoline, and ketanserin and also lysergic acid diethylamide were applied by iontophoresis to firing CA1 hippocampal pyramidal cells to test their action on the inhibition produced by 5-hydroxytryptamine. In contrast to a previous report, none of these peripherally active 5-hydroxytryptamine antagonists altered the inhibitory response to submaximal doses of 5-hydroxytryptamine, but they did block after-excitations that followed the inhibitions. All the antagonists and lysergic acid diethylami

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47

Blaho, Kari, Kevin Merigian, Stephen Winbery, Stephen A. Geraci, and Chantay Smartt. "CLINICAL PHARMACOLOGY OF LYSERGIC ACID DIETHYLAMIDE." American Journal of Therapeutics 4, no. 5 (1997): 211. http://dx.doi.org/10.1097/00045391-199705000-00008.

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48

ABRAHAM, HENRY DAVID, and ANDREW M. ALDRIDGE. "Adverse consequences of lysergic acid diethylamide." Addiction 88, no. 10 (1993): 1327–34. http://dx.doi.org/10.1111/j.1360-0443.1993.tb02018.x.

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49

Hendrickson, James B., and Jian Wang. "A New Synthesis of Lysergic Acid." Organic Letters 6, no. 1 (2004): 3–5. http://dx.doi.org/10.1021/ol0354369.

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50

Cody, J. T., and S. Valtier. "Immunoassay Analysis of Lysergic Acid Diethylamide." Journal of Analytical Toxicology 21, no. 6 (1997): 459–64. http://dx.doi.org/10.1093/jat/21.6.459.

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