المؤلفون: Tuck, Jeremy Ryan

مصطلحات موضوعية: Organic chemistry, Neurosciences, Pharmacology, ergoline, isotryptamine, LSD, non-hallucinogenic, psychedelic, psychoplastogen

الوصول الحر: https://escholarship.org/uc/item/6g85p172Test

المؤلفون: Deokar, A. V.¹, Bhosle, P. V.

المصدر: Research Journal of Pharmacognosy and Phytochemistry 13(3):109-114. 2021

المؤلفون: Tamiris R. C. Silva, Cristiano Raminelli

المصدر: Química Nova, Vol 44, Iss 7, Pp 852-867 (2021)

مصطلحات موضوعية: total synthesis, formal synthesis, ergoline alkaloids, lysergic acid, Chemistry, QD1-999

وصف الملف: electronic resource

العلاقة: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422021000700852&tlng=ptTest; https://doaj.org/toc/1678-7064Test

الوصول الحر: https://doaj.org/article/55a46df85ffb4201900ce5f4840326d5Test

المؤلفون: Silva, Tamiris R. C., Raminelli, Cristiano

المصدر: Química Nova. January 2021 44(7)

مصطلحات موضوعية: total synthesis, formal synthesis, ergoline alkaloids, lysergic acid

وصف الملف: text/html

الوصول الحر: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422021000700852Test

المؤلفون: Yanisa Olaranont, Alyssa B. Stewart, Wisuwat Songnuan, Paweena Traiperm

المصدر: Journal of Fungi; Volume 8; Issue 8; Pages: 823

مصطلحات موضوعية: Clavicipitaceae, ergoline alkaloids, morning glory, plant–fungal symbiosis, secondary metabolites

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: https://dx.doi.org/10.3390/jof8080823Test

الإتاحة: https://doi.org/10.3390/jof8080823Test

المؤلفون: Meneghetti, Fiorella, Ferraboschi, Patrizia, Grisenti, Paride, Reza Elahi, Shahrzad, Mori, Matteo, Ciceri, Samuele

المساهمون: F. Meneghetti, P. Ferraboschi, P. Grisenti, S. Reza Elahi, M. Mori, S. Ciceri

مصطلحات موضوعية: 13C NMR, 15N NMR, 1H NMR, 9,10-unsaturated ergoline, X-ray analysi, alkaloid, ergot, oxytocic activity, Settore BIO/10 - Biochimica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31947568; info:eu-repo/semantics/altIdentifier/wos/WOS:000515381800093; volume:25; issue:2; firstpage:1; lastpage:11; numberofpages:11; journal:MOLECULES; http://hdl.handle.net/2434/706107Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85078003551

الإتاحة: https://doi.org/10.3390/molecules25020331Test
http://hdl.handle.net/2434/706107Test

المؤلفون: Fiorella Meneghetti, Patrizia Ferraboschi, Paride Grisenti, Shahrzad Reza Elahi, Matteo Mori, Samuele Ciceri

المصدر: Molecules; Volume 25; Issue 2; Pages: 331

مصطلحات موضوعية: ergot, 9,10-unsaturated ergoline, alkaloids, 15 N NMR, 13 C NMR, 1 H NMR, X-ray analysis, oxytocic activity

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: https://dx.doi.org/10.3390/molecules25020331Test

الإتاحة: https://doi.org/10.3390/molecules25020331Test

المؤلفون: Cristiano Raminelli, Tamiris R. C. Silva

المصدر: Química Nova, Vol 44, Iss 7, Pp 852-867 (2021)
Química Nova v.44 n.7 2021
Química Nova
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Química Nova, Volume: 44, Issue: 7, Pages: 852-867, Published: 03 SEP 2021

مصطلحات موضوعية: Lysergic acid, Formal synthesis, chemistry.chemical_compound, Chemistry, Stereochemistry, lysergic acid, Enantioselective synthesis, ergoline alkaloids, Total synthesis, total synthesis, QD1-999, formal synthesis

وصف الملف: text/html

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05790304192f9d7811bb081ca1828e74Test
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422021000700852&tlng=ptTest

المؤلفون: Beaulieu, Wesley T., Panaccione, Daniel G., Ryan, Katy L., Kaonongbua, Wittaya, Clay, Keith

المصدر: Mycologia, 2015 Jul 01. 107(4), 667-678.

الوصول الحر: https://www.jstor.org/stable/26506926Test

المؤلفون: María Isabel Loza, Rob Leurs, Chris de Graaf, András Visegrády, Attila Egyed, György M. Keserű, José Brea, Ádám Andor Kelemen, Stephanie A. Thee, Zhiyong Wang, Márton Vass

المساهمون: Medicinal chemistry, AIMMS

المصدر: Bioorganic Chemistry, 111:104832, 1-11. Academic Press Inc.
Egyed, A, Kelemen, Á A, Vass, M, Visegrády, A, Thee, S A, Wang, Z, de Graaf, C, Brea, J, Loza, M I, Leurs, R & Keserű, G M 2021, ' Controlling the selectivity of aminergic GPCR ligands from the extracellular vestibule ', Bioorganic Chemistry, vol. 111, 104832, pp. 1-11 . https://doi.org/10.1016/j.bioorg.2021.104832Test

مصطلحات موضوعية: Secondary binding pocket, Allosteric regulation, Pyrimidinones, Ligands, Biochemistry, Receptors, G-Protein-Coupled, Fragment linking, Structure-Activity Relationship, Docking (dog), GPCR, SDG 3 - Good Health and Well-being, Dopamine receptor D3, Drug Discovery, medicine, Humans, Urea, Selectivity, Receptor, Molecular Biology, G protein-coupled receptor, Virtual screening, Dose-Response Relationship, Drug, Molecular Structure, Ligand, Chemistry, Organic Chemistry, Ergoline, Bitopic ligand, Biophysics, Allosteric Site, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b05fe1ab8d56524eef48524ef62e088Test
https://doi.org/10.1016/j.bioorg.2021.104832Test