Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Przeglądasz jako GOŚĆ

Wyszukujesz frazę ""Alkaloids"" wg kryterium: Temat


Tytuł :
Macroline, talpinine, and sarpagine alkaloids from Alstonia penangiana. An NMR-based method for differentiating between A. penangiana and A. macrophylla.
Autorzy :
Yeap JS; Department of Chemistry, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Tan CH; Institute of Biological Sciences, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Yong KT; Institute of Biological Sciences, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Lim KH; School of Pharmacy, University of Nottingham Malaysia Campus, Jalan Broga, 43500, Semenyih, Selangor, Malaysia.
Lim SH; Department of Chemistry, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Low YY; Department of Chemistry, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia. Electronic address: .
Kam TS; Department of Chemistry, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia. Electronic address: .
Pokaż więcej
Źródło :
Phytochemistry [Phytochemistry] 2020 Aug; Vol. 176, pp. 112391. Date of Electronic Publication: 2020 May 06.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Elsevier Country of Publication: England NLM ID: 0151434 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-3700 (Electronic) Linking ISSN: 00319422 NLM ISO Abbreviation: Phytochemistry Subsets: MEDLINE
MeSH Terms :
Alkaloids*
Alstonia*
Humans ; Indole Alkaloids ; Molecular Structure ; Oxindoles
Czasopismo naukowe
Tytuł :
Cytotoxic monoterpenoid indole alkaloids from the aerial parts of Kopsia officinalis .
Autorzy :
Liu T; Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China.; Department of General Practice, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Hu J; College of Biological Resources and Food Engineering, Qujing Normal University, Qujing 655011, China.
Li JX; Tumor Hospital of Yunnan Province, The Third Affiliated Hospital of Kunming Medical University, Kunming 650118, China.
Chen MW; Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China.
Pokaż więcej
Źródło :
Journal of Asian natural products research [J Asian Nat Prod Res] 2020 Aug; Vol. 22 (8), pp. 724-731. Date of Electronic Publication: 2019 Jun 01.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Informa Healthcare Country of Publication: England NLM ID: 100888334 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-2213 (Electronic) Linking ISSN: 10286020 NLM ISO Abbreviation: J Asian Nat Prod Res Subsets: MEDLINE
MeSH Terms :
Antineoplastic Agents, Phytogenic*
Apocynaceae*
Secologanin Tryptamine Alkaloids*
Cell Line, Tumor ; Indole Alkaloids ; Molecular Structure ; Plant Components, Aerial
Czasopismo naukowe
Tytuł :
Alkaloid and iridoid glucosides from Palicourea luxurians (Rubiaceae: Palicoureeae) indicate tryptamine- and tryptophan-iridoid alkaloid formation apart the strictosidine pathway.
Autorzy :
Kornpointner C; Department of Organic Chemistry, University of Vienna, Währinger Strasse 38, A-1090, Vienna, Austria.
Berger A; Department of Botany and Biodiversity Research, University of Vienna, Rennweg 14, A-1030, Vienna, Austria.
Traxler F; Department of Organic Chemistry, University of Vienna, Währinger Strasse 38, A-1090, Vienna, Austria.
Hadžiabdić A; Department of Organic Chemistry, University of Vienna, Währinger Strasse 38, A-1090, Vienna, Austria.
Massar M; Department of Organic Chemistry, University of Vienna, Währinger Strasse 38, A-1090, Vienna, Austria.
Matek J; Department of Organic Chemistry, University of Vienna, Währinger Strasse 38, A-1090, Vienna, Austria.
Brecker L; Department of Organic Chemistry, University of Vienna, Währinger Strasse 38, A-1090, Vienna, Austria. Electronic address: .
Schinnerl J; Department of Botany and Biodiversity Research, University of Vienna, Rennweg 14, A-1030, Vienna, Austria. Electronic address: .
Pokaż więcej
Źródło :
Phytochemistry [Phytochemistry] 2020 May; Vol. 173, pp. 112296. Date of Electronic Publication: 2020 Feb 19.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Elsevier Country of Publication: England NLM ID: 0151434 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-3700 (Electronic) Linking ISSN: 00319422 NLM ISO Abbreviation: Phytochemistry Subsets: MEDLINE
MeSH Terms :
Alkaloids*
Rubiaceae*
Secologanin Tryptamine Alkaloids*
Iridoid Glucosides ; Iridoids ; Tryptamines ; Tryptophan ; Vinca Alkaloids
Czasopismo naukowe
Tytuł :
Biosynthesis-inspired mining and identification of untapped alkaloids in Camptotheca acuminate for enzyme discovery using ultra-high performance liquid chromatography coupled with quadrupole-time of flight-mass spectrometry.
Autorzy :
Pu X; College of Science, Sichuan Agricultural University, Ya'an 625014, China. Electronic address: .
Zhang CR; College of Science, Sichuan Agricultural University, Ya'an 625014, China.
Gao HC; College of Science, Sichuan Agricultural University, Ya'an 625014, China.
Gao YJ; College of Chemistry and Materials Science, Sichuan Normal University, Chengdu 610066, China.
Huang L; College of Science, Sichuan Agricultural University, Ya'an 625014, China.
Zhu L; College of Science, Sichuan Agricultural University, Ya'an 625014, China.
Rao Y; College of Science, Sichuan Agricultural University, Ya'an 625014, China.
Zhang S; College of Science, Sichuan Agricultural University, Ya'an 625014, China.
Jiang YY; College of Science, Sichuan Agricultural University, Ya'an 625014, China.
Zhang L; College of Science, Sichuan Agricultural University, Ya'an 625014, China.
Huang QM; College of Science, Sichuan Agricultural University, Ya'an 625014, China. Electronic address: .
Pokaż więcej
Źródło :
Journal of chromatography. A [J Chromatogr A] 2020 Jun 07; Vol. 1620, pp. 461036. Date of Electronic Publication: 2020 Mar 19.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Elsevier Country of Publication: Netherlands NLM ID: 9318488 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-3778 (Electronic) Linking ISSN: 00219673 NLM ISO Abbreviation: J Chromatogr A Subsets: MEDLINE
MeSH Terms :
Biosynthetic Pathways*
Alkaloids/*analysis
Camptotheca/*chemistry
Chromatography, High Pressure Liquid/*methods
Tandem Mass Spectrometry/*methods
Camptothecin/analogs & derivatives ; Camptothecin/analysis ; Camptothecin/chemistry ; Camptothecin/metabolism ; Carbolines/analysis ; Carbolines/chemistry ; Databases as Topic ; Discriminant Analysis ; Glycosides/analysis ; Glycosides/chemistry ; Indole Alkaloids/analysis ; Indole Alkaloids/chemistry ; Least-Squares Analysis ; Metabolic Networks and Pathways ; Metabolome ; Metabolomics ; Multivariate Analysis ; Principal Component Analysis
Czasopismo naukowe
Tytuł :
Straightforward synthesis, characterization, and cytotoxicity evaluation of hybrids of natural alkaloid evodiamine/rutaecarpine and thieno[2,3- d ]pyrimidinones.
Autorzy :
Nie LF; Key Laboratory of Plant Resources and Chemistry of Arid Zone, State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China.; University of Chinese Academy of Sciences, Beijing 100049, China.
Wang SS; College of Life and Environmental Sciences, Shanghai Normal University, Shanghai 201418, China.
Cao JG; College of Life and Environmental Sciences, Shanghai Normal University, Shanghai 201418, China.
Liu FZ; Key Laboratory of Plant Resources and Chemistry of Arid Zone, State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China.; University of Chinese Academy of Sciences, Beijing 100049, China.
Xiamuxi H; Key Laboratory of Plant Resources and Chemistry of Arid Zone, State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China.; University of Chinese Academy of Sciences, Beijing 100049, China.
Aisa HA; Key Laboratory of Plant Resources and Chemistry of Arid Zone, State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China.
Huang GZ; Key Laboratory of Plant Resources and Chemistry of Arid Zone, State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China.; College of Life and Environmental Sciences, Shanghai Normal University, Shanghai 201418, China.
Pokaż więcej
Źródło :
Journal of Asian natural products research [J Asian Nat Prod Res] 2020 Jan; Vol. 22 (1), pp. 69-82. Date of Electronic Publication: 2018 Dec 27.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Informa Healthcare Country of Publication: England NLM ID: 100888334 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-2213 (Electronic) Linking ISSN: 10286020 NLM ISO Abbreviation: J Asian Nat Prod Res Subsets: MEDLINE
MeSH Terms :
Alkaloids*
Antineoplastic Agents*
Carcinoma, Non-Small-Cell Lung*
Lung Neoplasms*
Humans ; Indole Alkaloids ; Molecular Structure ; Pyrimidinones ; Quinazolines ; Structure-Activity Relationship
Czasopismo naukowe
Tytuł :
HPLC-DAD-SPE-NMR isolation of tetracyclic spiro-alkaloids with antiplasmodial activity from the seeds of Erythrina latissima .
Autorzy :
Zarev Y; Natural Products & Food Research and Analysis (NatuRA), Department of Pharmaceutical Sciences, University of Antwerp, Antwerp, Belgium.; Department of Pharmacognosy, Faculty of Pharmacy, Medical University-Sofia, Sofia, Bulgaria.
Foubert K; Natural Products & Food Research and Analysis (NatuRA), Department of Pharmaceutical Sciences, University of Antwerp, Antwerp, Belgium.
Cos P; Laboratory for Microbiology, Parasitology and Hygiene (LMPH), Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium.
Maes L; Laboratory for Microbiology, Parasitology and Hygiene (LMPH), Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium.
Elgorashi E; Toxicology and Ethnoveterinary Medicine; Food, Feed and Veterinary Public Health, ARC-Onderstepoort Veterinary Institute, Onderstepoort, South-Africa.
Apers S; Natural Products & Food Research and Analysis (NatuRA), Department of Pharmaceutical Sciences, University of Antwerp, Antwerp, Belgium.
Ionkova I; Department of Pharmacognosy, Faculty of Pharmacy, Medical University-Sofia, Sofia, Bulgaria.
Pieters L; Natural Products & Food Research and Analysis (NatuRA), Department of Pharmaceutical Sciences, University of Antwerp, Antwerp, Belgium.
Pokaż więcej
Źródło :
Natural product research [Nat Prod Res] 2020 Apr; Vol. 34 (7), pp. 1037-1040. Date of Electronic Publication: 2019 Jan 03.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Taylor & Francis Health Sciences Country of Publication: England NLM ID: 101167924 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1478-6427 (Electronic) Linking ISSN: 14786419 NLM ISO Abbreviation: Nat. Prod. Res. Subsets: MEDLINE
MeSH Terms :
Alkaloids/*isolation & purification
Alkaloids/*pharmacology
Antimalarials/*isolation & purification
Erythrina/*chemistry
Plant Extracts/*chemistry
Alkaloids/chemistry ; Antimalarials/chemistry ; Cell Line ; Chloroquine/pharmacology ; Chromatography, High Pressure Liquid ; Dihydro-beta-Erythroidine/analogs & derivatives ; Drug Resistance ; Humans ; Indole Alkaloids ; Magnetic Resonance Spectroscopy ; Plant Extracts/analysis ; Plant Extracts/pharmacology ; Plasmodium falciparum/drug effects ; Seeds/chemistry
Czasopismo naukowe
Tytuł :
Structural basis of cycloaddition in biosynthesis of iboga and aspidosperma alkaloids.
Autorzy :
Caputi L; Max Planck Institute of Chemical Ecology, Department of Natural Product Biosynthesis, Jena, Germany.
Franke J; Leibniz University Hannover, Centre for Biomolecular Drug Research, Hannover, Germany.
Bussey K; John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK.
Farrow SC; John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK.
Vieira IJC; Laboratorio de Ciencias Quimicas-UENF-Campos dos Goytacazes-RJ, Campos dos Goytacazes, Brazil.
Stevenson CEM; John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK.
Lawson DM; John Innes Centre, Department of Biological Chemistry, Norwich Research Park, Norwich, UK. .
O'Connor SE; Max Planck Institute of Chemical Ecology, Department of Natural Product Biosynthesis, Jena, Germany. .
Pokaż więcej
Źródło :
Nature chemical biology [Nat Chem Biol] 2020 Apr; Vol. 16 (4), pp. 383-386. Date of Electronic Publication: 2020 Feb 17.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
Journal Info :
Publisher: Nature Pub. Group Country of Publication: United States NLM ID: 101231976 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4469 (Electronic) Linking ISSN: 15524450 NLM ISO Abbreviation: Nat. Chem. Biol. Subsets: MEDLINE
MeSH Terms :
Alkaloids/*biosynthesis
Aspidosperma/*chemistry
Tabernaemontana/*chemistry
Alkaloids/chemistry ; Carbazoles/chemistry ; Cycloaddition Reaction/methods ; Indole Alkaloids/chemistry ; Plants/chemistry
Czasopismo naukowe
Tytuł :
A new indole alkaloid from Cimicifuga heracleifolia .
Autorzy :
Lu J; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences (CAS) , Kunming 650204 , China.; University of Chinese Academy of Sciences , Beijing 100049 , China.
Wang WH; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences (CAS) , Kunming 650204 , China.; University of Chinese Academy of Sciences , Beijing 100049 , China.
Shi QQ; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences (CAS) , Kunming 650204 , China.; University of Chinese Academy of Sciences , Beijing 100049 , China.
Peng XR; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences (CAS) , Kunming 650204 , China.
Li DS; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences (CAS) , Kunming 650204 , China.
Qiu MH; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences (CAS) , Kunming 650204 , China.; University of Chinese Academy of Sciences , Beijing 100049 , China.
Pokaż więcej
Źródło :
Journal of Asian natural products research [J Asian Nat Prod Res] 2019 Nov; Vol. 21 (11), pp. 1119-1122. Date of Electronic Publication: 2018 Nov 17.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Informa Healthcare Country of Publication: England NLM ID: 100888334 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-2213 (Electronic) Linking ISSN: 10286020 NLM ISO Abbreviation: J Asian Nat Prod Res Subsets: MEDLINE
MeSH Terms :
Alkaloids*
Cimicifuga*
Indole Alkaloids ; Molecular Structure
Czasopismo naukowe
Tytuł :
Common anticholinergic solanaceaous plants of temperate Europe - A review of intoxications from the literature (1966-2018).
Autorzy :
Fatur K; Faculty of Pharmacy, University of Ljubljana, Tržaška Cesta 32, 1000, Ljubljana, Slovenia. Electronic address: .
Kreft S; Faculty of Pharmacy, University of Ljubljana, Tržaška Cesta 32, 1000, Ljubljana, Slovenia.
Pokaż więcej
Źródło :
Toxicon : official journal of the International Society on Toxinology [Toxicon] 2020 Apr 15; Vol. 177, pp. 52-88. Date of Electronic Publication: 2020 Feb 13.
Typ publikacji :
Journal Article; Review
Journal Info :
Publisher: Pergamon Press Country of Publication: England NLM ID: 1307333 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-3150 (Electronic) Linking ISSN: 00410101 NLM ISO Abbreviation: Toxicon Subsets: MEDLINE
MeSH Terms :
Solanaceae*
Cholinergic Antagonists/*toxicity
Plant Extracts/*toxicity
Plant Poisoning/*epidemiology
Solanaceous Alkaloids/*toxicity
Alkaloids ; Atropa belladonna ; Europe ; Humans ; Hyoscyamus ; Scopolamine ; Scopolia ; Tropanes
Czasopismo naukowe
Tytuł :
Gigantelline, gigantellinine and gigancrinine, cherylline- and crinine-type alkaloids isolated from Crinum jagus with anti-acetylcholinesterase activity.
Autorzy :
Ka S; Département de Chimie, Biochimie et Physique, Université du Québec à Trois-Rivières, 3351, Boul. des Forges, C.P. 500, Trois-Rivières, Québec, G8Z 4M3, Canada; Laboratoire de Chimie Organique et Chimie Thérapeutique, Faculté de Médecine, de Pharmacie et d'Odontologie de Dakar, Dakar, Sénégal.
Masi M; Dipartimento di Scienze Chimiche, Universita' di Napoli Federico II, Complesso Universitario Monte Sant'Angelo, Via Cintia 4, 80126 Napoli, Italy.
Merindol N; Département de Chimie, Biochimie et Physique, Université du Québec à Trois-Rivières, 3351, Boul. des Forges, C.P. 500, Trois-Rivières, Québec, G8Z 4M3, Canada.
Di Lecce R; Dipartimento di Scienze Chimiche, Universita' di Napoli Federico II, Complesso Universitario Monte Sant'Angelo, Via Cintia 4, 80126 Napoli, Italy.
Plourde MB; Département de Chimie, Biochimie et Physique, Université du Québec à Trois-Rivières, 3351, Boul. des Forges, C.P. 500, Trois-Rivières, Québec, G8Z 4M3, Canada.
Seck M; Laboratoire de Chimie Organique et Chimie Thérapeutique, Faculté de Médecine, de Pharmacie et d'Odontologie de Dakar, Dakar, Sénégal.
Górecki M; Dipartimento di Chimica e Chimica Industriale, Università di Pisa, Via Giuseppe Moruzzi, 13, 56124, Pisa, Italy; Institute of Organic Chemistry, Polish Academy of Sciences, ul. Kasprzaka 44/52, Warsaw, 01-224, Poland.
Pescitelli G; Dipartimento di Chimica e Chimica Industriale, Università di Pisa, Via Giuseppe Moruzzi, 13, 56124, Pisa, Italy.
Desgagne-Penix I; Département de Chimie, Biochimie et Physique, Université du Québec à Trois-Rivières, 3351, Boul. des Forges, C.P. 500, Trois-Rivières, Québec, G8Z 4M3, Canada. Electronic address: .
Evidente A; Dipartimento di Scienze Chimiche, Universita' di Napoli Federico II, Complesso Universitario Monte Sant'Angelo, Via Cintia 4, 80126 Napoli, Italy. Electronic address: .
Pokaż więcej
Źródło :
Phytochemistry [Phytochemistry] 2020 Jul; Vol. 175, pp. 112390. Date of Electronic Publication: 2020 Apr 23.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Elsevier Country of Publication: England NLM ID: 0151434 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-3700 (Electronic) Linking ISSN: 00319422 NLM ISO Abbreviation: Phytochemistry Subsets: MEDLINE
MeSH Terms :
Alkaloids*
Amaryllidaceae Alkaloids*
Crinum*
Isoquinolines ; Molecular Structure
Czasopismo naukowe
Tytuł :
Narciclasine-4- O - β -D-xylopyranoside, a new narciclasine glycoside from Zephyranthes minuta .
Autorzy :
Katoch D; Academy of Scientific & Innovative Research, CSIR-IHBT, Palampur, Himachal Pradesh, India.; Natural Product Chemistry and Process Development Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, Himachal Pradesh, India.
Kumar D; Department of Food and Nutraceuticals, CSIR-Institute of Himalayan Bioresource Technology, Palampur, Himachal Pradesh, India.
Padwad YS; Academy of Scientific & Innovative Research, CSIR-IHBT, Palampur, Himachal Pradesh, India.; Department of Food and Nutraceuticals, CSIR-Institute of Himalayan Bioresource Technology, Palampur, Himachal Pradesh, India.
Singh B; Academy of Scientific & Innovative Research, CSIR-IHBT, Palampur, Himachal Pradesh, India.; Natural Product Chemistry and Process Development Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, Himachal Pradesh, India.
Sharma U; Academy of Scientific & Innovative Research, CSIR-IHBT, Palampur, Himachal Pradesh, India.; Natural Product Chemistry and Process Development Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, Himachal Pradesh, India.
Pokaż więcej
Źródło :
Natural product research [Nat Prod Res] 2020 Jan; Vol. 34 (2), pp. 233-240. Date of Electronic Publication: 2019 Jan 12.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Taylor & Francis Health Sciences Country of Publication: England NLM ID: 101167924 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1478-6427 (Electronic) Linking ISSN: 14786419 NLM ISO Abbreviation: Nat. Prod. Res. Subsets: MEDLINE
MeSH Terms :
Amaryllidaceae/*chemistry
Amaryllidaceae Alkaloids/*isolation & purification
Glycosides/*isolation & purification
Phenanthridines/*isolation & purification
Alkaloids/chemistry ; Alkaloids/pharmacology ; Amaryllidaceae Alkaloids/chemistry ; Amaryllidaceae Alkaloids/pharmacology ; Cardiac Glycosides ; Cell Line, Tumor ; Cytotoxins/isolation & purification ; Cytotoxins/pharmacology ; Glycosides/chemistry ; Humans ; Isoquinolines/pharmacology ; Phenanthridines/chemistry ; Phenanthridines/pharmacology ; Plant Extracts/chemistry
Czasopismo naukowe
Tytuł :
Structurally diverse and bioactive alkaloids from an insect-derived fungus Neosartorya fischeri.
Autorzy :
Lin S; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
He Y; Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Li F; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Yang B; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Liu M; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Zhang S; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Liu J; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Li H; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Qi C; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Wang J; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Hu Z; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China. Electronic address: .
Zhang Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China. Electronic address: .
Pokaż więcej
Źródło :
Phytochemistry [Phytochemistry] 2020 Jul; Vol. 175, pp. 112374. Date of Electronic Publication: 2020 Apr 18.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Elsevier Country of Publication: England NLM ID: 0151434 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-3700 (Electronic) Linking ISSN: 00319422 NLM ISO Abbreviation: Phytochemistry Subsets: MEDLINE
MeSH Terms :
Alkaloids*
Neosartorya*
Animals ; Aspergillus ; Escherichia coli ; Insecta ; Mice
Czasopismo naukowe
Tytuł :
Three new isoquinoline alkaloids from the whole plants of Thalictrum tenue with cytotoxic activities.
Autorzy :
Xu L; Department of Oncology, General Hospital of Northern Theater Command, Shenyang 110016, China.
Yang W; Department of Thoracic Surgery, Shengjing Hospital of China Medical University, Shenyang 110004, China.
Hu J; College of Biological Resources and Food Engineering, Qujing Normal University, Qujing 655011, China.
Han CM; Department of Oncology, Liaoyang City Third People's Hospital, Liaoyang 111000, China.
Li PF; Department of Thoracic Surgery 4, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang 110042, China.
Pokaż więcej
Źródło :
Journal of Asian natural products research [J Asian Nat Prod Res] 2020 Jul; Vol. 22 (7), pp. 618-625. Date of Electronic Publication: 2019 May 03.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Informa Healthcare Country of Publication: England NLM ID: 100888334 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-2213 (Electronic) Linking ISSN: 10286020 NLM ISO Abbreviation: J Asian Nat Prod Res Subsets: MEDLINE
MeSH Terms :
Alkaloids*
Antineoplastic Agents, Phytogenic*
Thalictrum*
Cell Line, Tumor ; Isoquinolines ; Molecular Structure
Czasopismo naukowe
Tytuł :
Formal enantioselective total synthesis of bisdehydroneostemoninine.
Autorzy :
Ma KQ; Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan 030006, China.
Ren HB; Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan 030006, China.; College of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006, China.
Chao JB; Scientific Instrument Center, Shanxi University, Taiyuan 030006, China.
Qin XM; Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan 030006, China.
Pokaż więcej
Źródło :
Journal of Asian natural products research [J Asian Nat Prod Res] 2020 Jul; Vol. 22 (7), pp. 655-662. Date of Electronic Publication: 2019 May 03.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Informa Healthcare Country of Publication: England NLM ID: 100888334 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-2213 (Electronic) Linking ISSN: 10286020 NLM ISO Abbreviation: J Asian Nat Prod Res Subsets: MEDLINE
MeSH Terms :
Alkaloids*
Cyclization ; Epoxy Compounds ; Molecular Structure ; Stereoisomerism
Czasopismo naukowe
Tytuł :
Pesimquinolones produced by Penicillium simplicissimum and their inhibitory activity on nitric oxide production.
Autorzy :
Dai C; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Chen C; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Guan D; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Chen H; Faculty of Medicine, Dentistry and Health, University of Sheffield, South Yorkshire, Sheffield, United Kingdom.
Wang F; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Wang W; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Zang Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Li Q; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Wei M; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Li X; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Zhang X; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Wang J; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Zhou Q; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China. Electronic address: .
Zhu H; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China. Electronic address: .
Zhang Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China. Electronic address: .
Pokaż więcej
Źródło :
Phytochemistry [Phytochemistry] 2020 Jun; Vol. 174, pp. 112327. Date of Electronic Publication: 2020 Mar 26.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Elsevier Country of Publication: England NLM ID: 0151434 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-3700 (Electronic) Linking ISSN: 00319422 NLM ISO Abbreviation: Phytochemistry Subsets: MEDLINE
MeSH Terms :
Alkaloids*
Penicillium*
Anti-Inflammatory Agents ; Molecular Structure ; Nitric Oxide
Czasopismo naukowe
Tytuł :
Tropolone alkaloids from Colchicum kurdicum (Bornm.) Stef. (Colchicaceae) as the potent novel antileishmanial compounds; purification, structure elucidation, antileishmanial activities and molecular docking studies.
Autorzy :
Azadbakht M; Department of Pharmacognosy and Biotechnology, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Davoodi A; Department of Pharmacognosy and Biotechnology, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran. Electronic address: .
Hosseinimehr SJ; Department of Radiopharmacy, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Keighobadi M; Toxoplasmosis Research Center, Department of Parasitology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Fakhar M; Toxoplasmosis Research Center, Department of Parasitology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Valadan R; Department of Immunology and Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran.
Faridnia R; Toxoplasmosis Research Center, Department of Parasitology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Emami S; Department of Medicinal Chemistry and Pharmaceutical Sciences Research Center, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Azadbakht M; Department of Plant Systematics, High Educational of Sanna Institute, Sari, Iran.
Bakhtiyari A; Department of Pharmacognosy and Biotechnology, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Pokaż więcej
Źródło :
Experimental parasitology [Exp Parasitol] 2020 Jun; Vol. 213, pp. 107902. Date of Electronic Publication: 2020 Apr 27.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Academic Press Country of Publication: United States NLM ID: 0370713 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1090-2449 (Electronic) Linking ISSN: 00144894 NLM ISO Abbreviation: Exp. Parasitol. Subsets: MEDLINE
MeSH Terms :
Alkaloids/*pharmacology
Colchicum/*chemistry
Leishmania major/*drug effects
Plant Extracts/*pharmacology
Trypanocidal Agents/*pharmacology
Alkaloids/chemistry ; Alkaloids/isolation & purification ; Molecular Docking Simulation ; Plant Extracts/chemistry ; Plant Extracts/isolation & purification ; Tropolone/chemistry ; Trypanocidal Agents/chemistry ; Trypanocidal Agents/isolation & purification
Czasopismo naukowe
Tytuł :
Amaryllidaceae and Sceletium alkaloids.
Autorzy :
Jin Z; State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China. .
Yao G
Pokaż więcej
Źródło :
Natural product reports [Nat Prod Rep] 2019 Oct 16; Vol. 36 (10), pp. 1462-1488.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Review
Journal Info :
Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 8502408 Publication Model: Print Cited Medium: Internet ISSN: 1460-4752 (Electronic) Linking ISSN: 02650568 NLM ISO Abbreviation: Nat Prod Rep Subsets: MEDLINE
MeSH Terms :
Aizoaceae/*chemistry
Amaryllidaceae/*metabolism
Amaryllidaceae Alkaloids/*chemistry
Amaryllidaceae Alkaloids/*pharmacology
Alkaloids/chemistry ; Alkaloids/isolation & purification ; Alkaloids/pharmacology ; Amaryllidaceae/chemistry ; Animals ; Anti-Inflammatory Agents, Non-Steroidal/chemistry ; Anti-Inflammatory Agents, Non-Steroidal/pharmacology ; Anti-Obesity Agents/chemistry ; Anti-Obesity Agents/pharmacology ; Antineoplastic Agents, Phytogenic/chemistry ; Antineoplastic Agents, Phytogenic/pharmacology ; Antiviral Agents/chemistry ; Antiviral Agents/pharmacology ; Humans ; Molecular Structure
Czasopismo naukowe
Tytuł :
Structure-function studies of tetrahydroprotoberberine N -methyltransferase reveal the molecular basis of stereoselective substrate recognition.
Autorzy :
Lang DE; Department of Biological Sciences, University of Calgary, Calgary, Alberta T2N 1N4, Canada.
Morris JS; Department of Biological Sciences, University of Calgary, Calgary, Alberta T2N 1N4, Canada.
Rowley M; Department of Biological Sciences, University of Calgary, Calgary, Alberta T2N 1N4, Canada.
Torres MA; Department of Biological Sciences, University of Calgary, Calgary, Alberta T2N 1N4, Canada.; Department of Structural Biology, Stanford University School of Medicine, Stanford, California 94305.
Maksimovich VA; Department of Biological Sciences, University of Calgary, Calgary, Alberta T2N 1N4, Canada.
Facchini PJ; Department of Biological Sciences, University of Calgary, Calgary, Alberta T2N 1N4, Canada.
Ng KKS; Department of Biological Sciences, University of Calgary, Calgary, Alberta T2N 1N4, Canada .
Pokaż więcej
Źródło :
The Journal of biological chemistry [J Biol Chem] 2019 Oct 04; Vol. 294 (40), pp. 14482-14498. Date of Electronic Publication: 2019 Aug 07.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
Journal Info :
Publisher: American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID: 2985121R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1083-351X (Electronic) Linking ISSN: 00219258 NLM ISO Abbreviation: J. Biol. Chem. Subsets: MEDLINE
MeSH Terms :
Protein Conformation*
Structure-Activity Relationship*
Berberine Alkaloids/*chemistry
Methyltransferases/*ultrastructure
Alkaloids/chemistry ; Alkaloids/metabolism ; Benzylisoquinolines/chemistry ; Benzylisoquinolines/metabolism ; Berberine Alkaloids/metabolism ; Binding Sites/genetics ; Crystallography, X-Ray ; Methyltransferases/chemistry ; Methyltransferases/metabolism ; Mutagenesis ; Protein Binding/genetics ; Ranunculales/enzymology ; S-Adenosylmethionine/chemistry ; S-Adenosylmethionine/metabolism
Czasopismo naukowe
Tytuł :
Piperine ameliorated memory impairment and myelin damage in lysolecethin induced hippocampal demyelination.
Autorzy :
Roshanbakhsh H; Faculty of Biology, Damghan University, Damghan, Iran.
Elahdadi Salmani M; Faculty of Biology, Damghan University, Damghan, Iran.
Dehghan S; Physiology Department, School of Medicine, Tarbiat modares University, Tehran, Iran.
Nazari A; Neuroscience Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
Javan M; Physiology Department, School of Medicine, Tarbiat modares University, Tehran, Iran.
Pourabdolhossein F; Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran; Neuroscience Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran. Electronic address: .
Pokaż więcej
Źródło :
Life sciences [Life Sci] 2020 Jul 15; Vol. 253, pp. 117671. Date of Electronic Publication: 2020 Apr 24.
Typ publikacji :
Journal Article
Journal Info :
Publisher: Elsevier Country of Publication: Netherlands NLM ID: 0375521 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0631 (Electronic) Linking ISSN: 00243205 NLM ISO Abbreviation: Life Sci. Subsets: MEDLINE
MeSH Terms :
Alkaloids/*pharmacology
Benzodioxoles/*pharmacology
Demyelinating Diseases/*drug therapy
Hippocampus/*drug effects
Lysophosphatidylcholines/*metabolism
Memory Disorders/*drug therapy
Myelin Sheath/*drug effects
Piperidines/*pharmacology
Polyunsaturated Alkamides/*pharmacology
Alkaloids/metabolism ; Animals ; Antioxidants/metabolism ; Antioxidants/pharmacology ; Benzodioxoles/metabolism ; Cytokines/genetics ; Cytokines/metabolism ; Gene Expression Regulation/drug effects ; Male ; Maze Learning/drug effects ; Models, Animal ; Neuroprotective Agents/metabolism ; Neuroprotective Agents/pharmacology ; Piperidines/metabolism ; Polyunsaturated Alkamides/metabolism ; Rats ; Rats, Wistar ; Spatial Memory/drug effects
Czasopismo naukowe
Tytuł :
Anti-tick effect and cholinesterase inhibition caused by Prosopis juliflora alkaloids: in vitro and in silico studies.
Autorzy :
Lima HG; Laboratório de Toxicologia, Departamento de Anatomia, Patologia e Clínicas, Hospital de Medicina Veterinária, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Santos FO; Laboratório de Toxicologia, Departamento de Anatomia, Patologia e Clínicas, Hospital de Medicina Veterinária, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Santos ACV; Laboratório de Toxicologia, Departamento de Anatomia, Patologia e Clínicas, Hospital de Medicina Veterinária, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Silva GDD; Laboratório de Toxicologia, Departamento de Anatomia, Patologia e Clínicas, Hospital de Medicina Veterinária, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Santos RJD; Laboratório de Toxicologia, Departamento de Anatomia, Patologia e Clínicas, Hospital de Medicina Veterinária, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Carneiro KO; Departamento de Saúde, Universidade Estadual de Feira de Santana - UEFS, Feira de Santana, BA, Brasil.
Reis IMA; Departamento de Saúde, Universidade Estadual de Feira de Santana - UEFS, Feira de Santana, BA, Brasil.
Estrela IO; Laboratório de Bioinformática e Modelagem Molecular - LaBiMM, Departamento do Medicamento, Faculdade de Farmácia, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Freitas HF; Laboratório de Bioinformática e Modelagem Molecular - LaBiMM, Departamento do Medicamento, Faculdade de Farmácia, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Bahiense TC; Departamento de Biointeração, Instituto de Ciências da Saúde, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Pita SSDR; Laboratório de Bioinformática e Modelagem Molecular - LaBiMM, Departamento do Medicamento, Faculdade de Farmácia, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Uzeda RS; Departamento de Medicina Veterinária Preventiva e Produção Animal, Escola de Medicina Veterinária e Zootecnia, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Branco A; Departamento de Saúde, Universidade Estadual de Feira de Santana - UEFS, Feira de Santana, BA, Brasil.
Costa SL; Departamento de Bioquímica e Biofísica, Instituto de Ciências da Saúde, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Batatinha MJM; Laboratório de Toxicologia, Departamento de Anatomia, Patologia e Clínicas, Hospital de Medicina Veterinária, Universidade Federal da Bahia - UFBA, Salvador, BA, Brasil.
Botura MB; Departamento de Saúde, Universidade Estadual de Feira de Santana - UEFS, Feira de Santana, BA, Brasil.
Pokaż więcej
Źródło :
Revista brasileira de parasitologia veterinaria = Brazilian journal of veterinary parasitology : Orgao Oficial do Colegio Brasileiro de Parasitologia Veterinaria [Rev Bras Parasitol Vet] 2020 Jun 26; Vol. 29 (2), pp. e019819. Date of Electronic Publication: 2020 Jun 26 (Print Publication: 2020).
Typ publikacji :
Journal Article
Journal Info :
Publisher: Colégio Brasileiro de Parasitologia Veterinária Country of Publication: Brazil NLM ID: 9440482 Publication Model: eCollection Cited Medium: Internet ISSN: 1984-2961 (Electronic) Linking ISSN: 0103846X NLM ISO Abbreviation: Rev Bras Parasitol Vet Subsets: MEDLINE
MeSH Terms :
Alkaloids*/pharmacology
Cholinesterases*/metabolism
Plant Extracts*/pharmacology
Prosopis*/chemistry
Rhipicephalus*/drug effects
Rhipicephalus*/enzymology
Acaricides/pharmacology ; Animals ; Chromatography, Liquid ; Enzyme Activation/drug effects ; Larva ; Molecular Docking Simulation ; Tandem Mass Spectrometry
Czasopismo naukowe

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies