المؤلفون: Yi Chen, Song-Wei Li, Fang-Zhou Yin, Min Yang, Xia-Juan Huan, Ze-Hong Miao, Xiao-Ming Wang, Yue-Wei Guo

المصدر: Natural Products and Bioprospecting, Vol 11, Iss 1, Pp 73-79 (2020)

مصطلحات موضوعية: Lagerstroemia indica Linnaeus, Pyrrole alkaloid, Total synthesis, Stereochemistry, Cytotoxicity, Botany, QK1-989

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2192-2195; https://doaj.org/toc/2192-2209

URL الوصول: https://doaj.org/article/1a0a037f41294675a63ee2710baeed29

المؤلفون: Toshio Sakamoto, Ayaka Nishida, Naoki Wada, Yutaka Nakamura, Shinji Sato, Tetsuya Konishi, Seiichi Matsugo

المصدر: Molecules; Volume 25; Issue 21; Pages: 4879

مصطلحات موضوعية: dietary supplement, edible fungus, pyrrole alkaloid

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: https://dx.doi.org/10.3390/molecules25214879

الاتاحة: https://doi.org/10.3390/molecules25214879

المؤلفون: Reddy, Chada Raji, Tukaram, Amol Gorgile, Mohammed, Siddique Z., Dilipkumar, Uredi, Babu, Bathini Nagendra, Chakravarty, Sumana, Bhattacharya, Dwaipayan, Joshi, Pranav C., Grée, René

المساهمون: CSIR Indian Institute of Chemical Technology (IICT), National Institute of Pharmaceutical Education and Research (NIPER), Institut des Sciences Chimiques de Rennes (ISCR), Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), CSIR, New Delhi, CNRS, CSIR, University of Rennes 1

المصدر: ISSN: 0960-894X ; Bioorganic and Medicinal Chemistry Letters ; https://univ-rennes.hal.science/hal-01737386 ; Bioorganic and Medicinal Chemistry Letters, 2018, 28 (4), pp.673-676. ⟨10.1016/j.bmcl.2018.01.020⟩.

مصطلحات موضوعية: Pyrrole alkaloid, Longanlactone, Neurotrophic agent, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry

Relation: info:eu-repo/semantics/altIdentifier/pmid/29402744; hal-01737386; https://univ-rennes.hal.science/hal-01737386; https://univ-rennes.hal.science/hal-01737386/document; https://univ-rennes.hal.science/hal-01737386/file/Reddy%20et%20al_Synthesis%20and%20biological%20evaluation%20of%20longanlactone%20analogues%20as%20neurotrophic.pdf; PUBMED: 29402744

الاتاحة: https://univ-rennes.hal.science/hal-01737386
https://univ-rennes.hal.science/hal-01737386/document
https://univ-rennes.hal.science/hal-01737386/file/Reddy%20et%20al_Synthesis%20and%20biological%20evaluation%20of%20longanlactone%20analogues%20as%20neurotrophic.pdf
https://doi.org/10.1016/j.bmcl.2018.01.020

المؤلفون: Sio-Hong Lam, Po-Hsun Chen, Hsin-Yi Hung, Tsong-Long Hwang, Chih-Chao Chiang, Tran Dinh Thang, Ping-Chung Kuo, Tian-Shung Wu

المصدر: Molecules; Volume 23; Issue 10; Pages: 2541

مصطلحات موضوعية: Menispermaceae, lignan, pyrrole alkaloid, superoxide anion generation, elastase release

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Natural Products Chemistry; https://dx.doi.org/10.3390/molecules23102541

الاتاحة: https://doi.org/10.3390/molecules23102541

المؤلفون: Toshio, Sakamoto, Ayaka, Nishida, Naoki, Wada, Yutaka, Nakamura, Shinji, Sato, Tetsuya, Konishi, Seiichi, Matsugo

المصدر: Molecules

مصطلحات موضوعية: Aldehydes, Magnetic Resonance Spectroscopy, edible fungus, Basidiomycota, Iron, Free Radical Scavengers, Acetates, Complex Mixtures, Mass Spectrometry, Article, Alkaloids, dietary supplement, Dietary Supplements, Solvents, Pyrroles, pyrrole alkaloid, Copper

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::2aa675baa6c0f7beb8beb98dee1b080a
https://pubmed.ncbi.nlm.nih.gov/33105737

المؤلفون: Hsin Yi Hung, Tran Dinh Thang, Ping Chung Kuo, Sio Hong Lam, Chih Chao Chiang, Tsong-Long Hwang, Tian Shung Wu, Po Hsun Chen

المصدر: Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 23, Iss 10, p 2541 (2018)
Molecules
Volume 23
Issue 10

مصطلحات موضوعية: lignan, Tinospora, Stereochemistry, Cytochalasin B, Neutrophils, Pharmaceutical Science, Phenylalanine, Menispermaceae, 01 natural sciences, Lignans, Article, Analytical Chemistry, lcsh:QD241-441, chemistry.chemical_compound, Alkaloids, lcsh:Organic chemistry, Superoxides, Drug Discovery, Humans, Pyrroles, Physical and Theoretical Chemistry, superoxide anion generation, Lignan, biology, Molecular Structure, Pancreatic Elastase, Plant Stems, 010405 organic chemistry, Superoxide, Alkaloid, Organic Chemistry, Elastase, Biological activity, elastase release, biology.organism_classification, 0104 chemical sciences, 010404 medicinal & biomolecular chemistry, chemistry, Chemistry (miscellaneous), Molecular Medicine, pyrrole alkaloid

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c83b9054f0e512cf189b7e854bddb370
https://pubmed.ncbi.nlm.nih.gov/30301176

المؤلفون: Siddique Z. Mohammed, Chada Raji Reddy, Dwaipayan Bhattacharya, Bathini Nagendra Babu, Sumana Chakravarty, René Grée, Uredi Dilipkumar, Amol Gorgile Tukaram, Pranav Chintamani Joshi

المساهمون: CSIR Indian Institute of Chemical Technology (IICT), National Institute of Pharmaceutical Education and Research (NIPER), Institut des Sciences Chimiques de Rennes (ISCR), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Université de Rennes (UNIV-RENNES)-Institut National des Sciences Appliquées (INSA), CSIR, New Delhi, CNRS, CSIR, University of Rennes 1, Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2018, 28 (4), pp.673-676. ⟨10.1016/j.bmcl.2018.01.020⟩
Bioorganic and Medicinal Chemistry Letters, 2018, 28 (4), pp.673-676. ⟨10.1016/j.bmcl.2018.01.020⟩

مصطلحات موضوعية: 0301 basic medicine, Neurite, Neurotrophic agent, Neuronal Outgrowth, Clinical Biochemistry, Pharmaceutical Science, Sonogashira coupling, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, 01 natural sciences, Biochemistry, Acylation, Lactones, Mice, 03 medical and health sciences, Longanlactone, Pyrrole alkaloid, Cell Line, Tumor, Drug Discovery, Animals, Pyrroles, RNA, Messenger, Molecular Biology, Biological evaluation, Molecular Structure, biology, 010405 organic chemistry, Chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Brain-Derived Neurotrophic Factor, Organic Chemistry, In vitro, 0104 chemical sciences, 030104 developmental biology, Real-time polymerase chain reaction, Drug Design, biology.protein, Molecular Medicine, Neurotrophin

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::709f58638d718961538645d4a045c7c5
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01737386

المؤلفون: Miyazaki, Mitsue, Kodrasov, Matthew P., Rotinsulu, Henki, Losung, Fitje, Mangindaan, Remy E.P., de Voogd, Nicole J., Yokosawa, Hideyoshi, Nicholson, Benjamin, Michitaka, Yamaguchi, Mitsue, Miyazaki, Matthew P., Kodrasov, Henki , Rotinsulu, Fitje, Losung, Remy E.P., Mangindaan, Nicole J., de Voogd, Benjamin, Nicholson, Sachiko, Tsukamoto

المصدر: Bioorganic & Medicinal Chemistry Letters. 23(13):3884-3886

مصطلحات موضوعية: Stereochemistry, Clinical Biochemistry, Pharmaceutical Science, Biochemistry, Ubiquitin-Specific Peptidase 7, Structure-Activity Relationship, chemistry.chemical_compound, Ubiquitin, Pyrrole alkaloid, 499.3, Drug Discovery, Animals, Humans, Structure–activity relationship, Protease Inhibitors, Pyrroles, USP7 inhibitor, Molecular Biology, Pyrrole, chemistry.chemical_classification, Isopeptide bond, Dose-Response Relationship, Drug, Molecular Structure, biology, Alkaloid, Organic Chemistry, biology.organism_classification, Spongiacidin C, Porifera, 483.2, Sponge, chemistry, Stylissa massa, biology.protein, Molecular Medicine, Ubiquitin Thiolesterase

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a5cdf5538f46b5f598ea5e583b755ea
http://hdl.handle.net/2298/00043539

المؤلفون: Li, Li-Ya, Ding, Yi, Groth, Ingrid, Menzel, Klaus-Dieter, Peschel, Gundela, Voigt, Kerstin, Deng, Zi-Wei, Sattler, Isabel, Lin, Wen-Han

المساهمون: Sattler, I (reprint author), Hans Knoell Inst, Leibniz Inst Nat Product Res & Infect Biol, Beutenbergstr 11A, D-07745 Jena, Germany., Hans Knoell Inst, Leibniz Inst Nat Product Res & Infect Biol, D-07745 Jena, Germany., Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100083, Peoples R China., Tsinghua Univ, Dept Biol Sci & Biotechnol, Beijing 100084, Peoples R China., Beijing Normal Univ, Analyt & Testing Ctr, Beijing 100875, Peoples R China., Hans Knoell Inst, Leibniz Inst Nat Product Res & Infect Biol, Beutenbergstr 11A, D-07745 Jena, Germany.

المصدر: SCI ; PubMed

مصطلحات موضوعية: Fusarium incarnatum, Aegiceras corniculatum, mangrove, pyrrole alkaloid, METABOLITES, DERIVATIVES, CONSTITUENTS

Relation: JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH.2008,10,(8),765-770.; 671418; http://hdl.handle.net/20.500.11897/156850; WOS:000258321500012

الاتاحة: https://hdl.handle.net/20.500.11897/156850
https://doi.org/10.1080/10286020802031106

المؤلفون: Yamaguchi, Michitaka, 165292, Miyazaki, Mitsue, 165358, Kodrasov, Matthew P., 165359, Rotinsulu, Henki, 165360, Losung, Fitje, 165361, Mangindaan, Remy E.P., 165362, de Voogd, Nicole J., 165363, Hideyoshi, Yokosawa, 165364, Nicholson, Benjamin, 165365, Tsukamoto, Sachiko, 165254

مصطلحات موضوعية: 483.2, 499.3, Spongiacidin C, Pyrrole alkaloid, Stylissa massa, USP7 inhibitor

وصف الملف: application/pdf

Relation: https://doi.org/10.1016/j.bmcl.2013.04.066; Bioorganic & Medicinal Chemistry Letters; 13; 23; 3884; 3886; https://kumadai.repo.nii.ac.jp/record/31915/files/0960-894Xv23_3884-3886.pdf

الاتاحة: https://kumadai.repo.nii.ac.jp/record/31915/files/0960-894Xv23_3884-3886.pdf