Informacja

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

Wyszukujesz frazę ""Indoles"" wg kryterium: Temat


Starter badań:

Tytuł:
Discovery of 5-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)-1H-indole-2-carboxamide derivatives as novel anti-cancer agents targeting Nur77.
Autorzy:
Qin J; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China.
Chen X; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China.
Liu W; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China.
Chen J; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China.
Liu W; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China.
Xia Y; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China.
Li Z; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China.
Li M; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China.
Wang S; State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, School of Public Health & School of Life Science, Xiamen, 361102, China.
Yuan Q; State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, School of Public Health & School of Life Science, Xiamen, 361102, China.
Qiu Y; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China. Electronic address: .
Wu Z; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China. Electronic address: .
Fang M; Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Science, Xiamen University, Xiamen, 361102, China. Electronic address: .
Pokaż więcej
Źródło:
European journal of medicinal chemistry [Eur J Med Chem] 2022 Dec 15; Vol. 244, pp. 114849. Date of Electronic Publication: 2022 Oct 14.
Typ publikacji:
Journal Article
MeSH Terms:
Antineoplastic Agents*/chemistry
Antineoplastic Agents*/pharmacology
Antineoplastic Agents*/therapeutic use
Carcinoma, Hepatocellular*/drug therapy
Indoles*/chemistry
Indoles*/pharmacology
Indoles*/therapeutic use
Liver Neoplasms*/drug therapy
Pentacyclic Triterpenes*/chemistry
Pentacyclic Triterpenes*/pharmacology
Pentacyclic Triterpenes*/therapeutic use
Nuclear Receptor Subfamily 4, Group A, Member 1*/antagonists & inhibitors
Humans ; Structure-Activity Relationship ; Apoptosis/drug effects ; Molecular Targeted Therapy
Czasopismo naukowe
Tytuł:
Bisindole natural products: A vital source for the development of new anticancer drugs.
Autorzy:
Xu M; School of Pharmacy, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China; Hubei Engineering Research Center of Traditional Chinese Medicine of South Hubei Province, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China.
Peng R; School of Pharmacy, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China; Hubei Engineering Research Center of Traditional Chinese Medicine of South Hubei Province, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China.
Min Q; School of Pharmacy, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China; Hubei Engineering Research Center of Traditional Chinese Medicine of South Hubei Province, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China.
Hui S; School of Pharmacy, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China; Hubei Engineering Research Center of Traditional Chinese Medicine of South Hubei Province, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China; Department of Hepatology, China Military Institute of Chinese Materia, The Fifth Medical Center of PLA General Hospital, PR China.
Chen X; School of Pharmacy, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China; Hubei Engineering Research Center of Traditional Chinese Medicine of South Hubei Province, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China.
Yang G; The State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University, Tianjin, PR China. Electronic address: .
Qin S; School of Pharmacy, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China; Hubei Engineering Research Center of Traditional Chinese Medicine of South Hubei Province, Xianning Medical College, Hubei University of Science and Technology, Xianning, PR China; Department of Hepatology, China Military Institute of Chinese Materia, The Fifth Medical Center of PLA General Hospital, PR China. Electronic address: .
Pokaż więcej
Źródło:
European journal of medicinal chemistry [Eur J Med Chem] 2022 Dec 05; Vol. 243, pp. 114748. Date of Electronic Publication: 2022 Sep 13.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Antineoplastic Agents*/chemistry
Antineoplastic Agents*/pharmacology
Biological Products*/pharmacology
Biological Products*/chemistry
Indole Alkaloids*/pharmacology
Indole Alkaloids*/chemistry
Indoles*/chemistry
Indoles*/pharmacology
Alkaloids ; Vincristine
Czasopismo naukowe
Tytuł:
Sonochemical synthesis and biological evaluation of isoquinolin-1(2H)-one/isoindolin-1-one derivatives: Discovery of a positive ago-allosteric modulator (PAAM) of 5HT2CR.
Autorzy:
Sandeep Kumar J; Dr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India.
Naimisha R; Dr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India.
Thirupataiah B; Dr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India.
Sujeevan Reddy G; Dr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India.
Bung N; TCS Research (Life Sciences Division), Tata Consultancy Services Limited, Hyderabad 500081, India.
Roy A; TCS Research (Life Sciences Division), Tata Consultancy Services Limited, Hyderabad 500081, India.
Bulusu G; Dr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India; TCS Research (Life Sciences Division), Tata Consultancy Services Limited, Hyderabad 500081, India; Center for Computational Natural Sciences and Bioinformatics, International Institute of Information Technology, Hyderabad 500 032, India.
Mishra A; Neuroscience & Ageing Biology, CSIR-Central Drug Research Institute (CSIR-CDRI), Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Yadav PN; Neuroscience & Ageing Biology, CSIR-Central Drug Research Institute (CSIR-CDRI), Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Misra P; Dr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India. Electronic address: .
Pal M; Dr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India. Electronic address: .
Pokaż więcej
Źródło:
Bioorganic chemistry [Bioorg Chem] 2022 Dec; Vol. 129, pp. 106202. Date of Electronic Publication: 2022 Oct 14.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Serotonin 5-HT2 Receptor Agonists*/chemical synthesis
Serotonin 5-HT2 Receptor Agonists*/chemistry
Serotonin 5-HT2 Receptor Agonists*/pharmacology
Isoquinolines*/chemical synthesis
Isoquinolines*/chemistry
Isoquinolines*/pharmacology
Indoles*/chemical synthesis
Indoles*/chemistry
Indoles*/pharmacology
Animals ; Male ; Mice ; Rats ; Brain ; Mice, Inbred BALB C
Czasopismo naukowe
Tytuł:
Angiogenesis and anti-leukaemia activity of novel indole derivatives as potent colchicine binding site inhibitors.
Autorzy:
Yao Y; Henan Provincial Key Laboratory of Pediatric Hematology, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou University, Zhengzhou, China.; School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan, China.; Ministry of Education of China, Key Laboratory of Advanced Drug Preparation Technologies (Zhengzhou University), Zhengzhou, China.
Huang T; Medical School, Huanghe Science and Technology University, Zhengzhou, Henan Province, P.R China.
Wang Y; School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Wang L; Henan Provincial Key Laboratory of Pediatric Hematology, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou University, Zhengzhou, China.
Feng S; School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan, China.; Ministry of Education of China, Key Laboratory of Advanced Drug Preparation Technologies (Zhengzhou University), Zhengzhou, China.
Cheng W; Henan Provincial Key Laboratory of Children's Genetics and Metabolic Diseases, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou University, Zhengzhou, China.
Yang L; School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan, China.; Ministry of Education of China, Key Laboratory of Advanced Drug Preparation Technologies (Zhengzhou University), Zhengzhou, China.
Duan Y; Henan Provincial Key Laboratory of Pediatric Hematology, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou University, Zhengzhou, China.; Henan Provincial Key Laboratory of Children's Genetics and Metabolic Diseases, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou University, Zhengzhou, China.
Pokaż więcej
Źródło:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2022 Dec; Vol. 37 (1), pp. 652-665.
Typ publikacji:
Journal Article
MeSH Terms:
Angiogenesis Inhibitors/*pharmacology
Antineoplastic Agents/*pharmacology
Colchicine/*antagonists & inhibitors
Indoles/*pharmacology
Neovascularization, Pathologic/*drug therapy
Tubulin Modulators/*pharmacology
Angiogenesis Inhibitors/chemical synthesis ; Angiogenesis Inhibitors/chemistry ; Animals ; Antineoplastic Agents/chemical synthesis ; Antineoplastic Agents/chemistry ; Apoptosis/drug effects ; Binding Sites/drug effects ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Colchicine/metabolism ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; Humans ; Indoles/chemical synthesis ; Indoles/chemistry ; Models, Molecular ; Molecular Structure ; Neoplasms, Experimental/drug therapy ; Neoplasms, Experimental/metabolism ; Neoplasms, Experimental/pathology ; Neovascularization, Pathologic/metabolism ; Neovascularization, Pathologic/pathology ; Structure-Activity Relationship ; Tubulin/metabolism ; Tubulin Modulators/chemical synthesis ; Tubulin Modulators/chemistry ; Zebrafish
Czasopismo naukowe
Tytuł:
Synthesis, molecular modelling and QSAR study of new N- phenylacetamide-2-oxoindole benzensulfonamide conjugates as carbonic anhydrase inhibitors with antiproliferative activity.
Autorzy:
Said MF; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
George RF; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Petreni A; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Florence, Italy.
Supuran CT; Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Florence, Italy.
Mohamed NM; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Modern University for Technology and Information MTI, Cairo, Egypt.
Pokaż więcej
Źródło:
Journal of enzyme inhibition and medicinal chemistry [J Enzyme Inhib Med Chem] 2022 Dec; Vol. 37 (1), pp. 701-717.
Typ publikacji:
Journal Article
MeSH Terms:
Quantitative Structure-Activity Relationship*
Acetanilides/*pharmacology
Antineoplastic Agents/*pharmacology
Carbonic Anhydrase Inhibitors/*pharmacology
Carbonic Anhydrases/*metabolism
Indoles/*pharmacology
Sulfonamides/*pharmacology
Acetanilides/chemical synthesis ; Acetanilides/chemistry ; Antineoplastic Agents/chemical synthesis ; Antineoplastic Agents/chemistry ; Carbonic Anhydrase Inhibitors/chemical synthesis ; Carbonic Anhydrase Inhibitors/chemistry ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Cell Survival/drug effects ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; Humans ; Indoles/chemical synthesis ; Indoles/chemistry ; Isoenzymes/antagonists & inhibitors ; Isoenzymes/metabolism ; Models, Molecular ; Molecular Structure ; Sulfonamides/chemical synthesis ; Sulfonamides/chemistry
Czasopismo naukowe
Tytuł:
Dearomative (3+2) Cycloadditions between Indoles and Vinyldiazo Species Enabled by a Red-Shifted Chromium Photocatalyst.
Autorzy:
Gall BK; Department of Chemistry, University of Georgia, Athens, GA 30602, USA.
Smith AK; Department of Chemistry, University of Georgia, Athens, GA 30602, USA.
Ferreira EM; Department of Chemistry, University of Georgia, Athens, GA 30602, USA.
Pokaż więcej
Źródło:
Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2022 Nov 07; Vol. 61 (45), pp. e202212187. Date of Electronic Publication: 2022 Oct 11.
Typ publikacji:
Journal Article
MeSH Terms:
Chromium*
Indoles*
Cycloaddition Reaction ; Cations
Czasopismo naukowe
Tytuł:
Selenium-Electrocatalytic Cyclization of 2-Vinylanilides towards Indoles of Peptide Labeling.
Autorzy:
Zeng S; International Cooperative Laboratory of Traditional Chinese Medicine Modernization, Innovative Drug Development of Chinese Ministry of Education, College of Pharmacy, Jinan University, Guangzhou, 510632, P.R. China.; Guangzhou Municipal and Guangdong Provincial Key Laboratory of Molecular Target & Clinical Pharmacology, The NMPA and State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences and the Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, 511436, P.R. China.
Fang S; International Cooperative Laboratory of Traditional Chinese Medicine Modernization, Innovative Drug Development of Chinese Ministry of Education, College of Pharmacy, Jinan University, Guangzhou, 510632, P.R. China.
Cai H; Guangzhou Municipal and Guangdong Provincial Key Laboratory of Molecular Target & Clinical Pharmacology, The NMPA and State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences and the Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, 511436, P.R. China.
Wang D; International Cooperative Laboratory of Traditional Chinese Medicine Modernization, Innovative Drug Development of Chinese Ministry of Education, College of Pharmacy, Jinan University, Guangzhou, 510632, P.R. China.
Liu W; International Cooperative Laboratory of Traditional Chinese Medicine Modernization, Innovative Drug Development of Chinese Ministry of Education, College of Pharmacy, Jinan University, Guangzhou, 510632, P.R. China.
Hu X; Guangzhou Municipal and Guangdong Provincial Key Laboratory of Molecular Target & Clinical Pharmacology, The NMPA and State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences and the Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, 511436, P.R. China.
Sun P; International Cooperative Laboratory of Traditional Chinese Medicine Modernization, Innovative Drug Development of Chinese Ministry of Education, College of Pharmacy, Jinan University, Guangzhou, 510632, P.R. China.
Ruan Z; Guangzhou Municipal and Guangdong Provincial Key Laboratory of Molecular Target & Clinical Pharmacology, The NMPA and State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences and the Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, 511436, P.R. China.
Pokaż więcej
Źródło:
Chemistry, an Asian journal [Chem Asian J] 2022 Oct 17; Vol. 17 (20), pp. e202200762. Date of Electronic Publication: 2022 Sep 08.
Typ publikacji:
Journal Article
MeSH Terms:
Indoles*/chemistry
Selenium*
Cyclization ; Catalysis ; Peptides ; Molecular Structure
Czasopismo naukowe
Tytuł:
Non-covalent small molecule partnership for redox-active films: Beyond polydopamine technology.
Autorzy:
Argenziano R; Department of Chemical Sciences, University of Naples 'Federico II', Via Cintia 21, I-80126 Naples, Italy.
Alfieri ML; Department of Chemical Sciences, University of Naples 'Federico II', Via Cintia 21, I-80126 Naples, Italy.
Arntz Y; Faculté de Chirurgie Dentaire, Université de Strasbourg, 8 rue Sainte Elisabeth, Strasbourg 67000, France.
Castaldo R; Institute for Polymers, Composites and Biomaterials - National Research Council of Italy, Via Campi Flegrei, 34, Pozzuoli, NA 80078, Italy.
Liberti D; Department of Chemical Sciences, University of Naples 'Federico II', Via Cintia 21, I-80126 Naples, Italy.
Maria Monti D; Department of Chemical Sciences, University of Naples 'Federico II', Via Cintia 21, I-80126 Naples, Italy.
Gentile G; Institute for Polymers, Composites and Biomaterials - National Research Council of Italy, Via Campi Flegrei, 34, Pozzuoli, NA 80078, Italy.
Panzella L; Department of Chemical Sciences, University of Naples 'Federico II', Via Cintia 21, I-80126 Naples, Italy.
Crescenzi O; Department of Chemical Sciences, University of Naples 'Federico II', Via Cintia 21, I-80126 Naples, Italy.
Ball V; Faculté de Chirurgie Dentaire, Université de Strasbourg, 8 rue Sainte Elisabeth, Strasbourg 67000, France.
Napolitano A; Department of Chemical Sciences, University of Naples 'Federico II', Via Cintia 21, I-80126 Naples, Italy. Electronic address: .
d'Ischia M; Department of Chemical Sciences, University of Naples 'Federico II', Via Cintia 21, I-80126 Naples, Italy.
Pokaż więcej
Źródło:
Journal of colloid and interface science [J Colloid Interface Sci] 2022 Oct 15; Vol. 624, pp. 400-410. Date of Electronic Publication: 2022 May 22.
Typ publikacji:
Journal Article
MeSH Terms:
Indoles*/chemistry
Indoles*/pharmacology
Polymers*/chemistry
Polymers*/pharmacology
Humans ; Oxidation-Reduction ; Technology
Czasopismo naukowe
Tytuł:
Manganese-Mediated Electrochemical Dearomatization of Indoles To Access 2-Azido Spirocyclic Indolines.
Autorzy:
Mo K; Institute of Drug Discovery Technology, Ningbo University, 315211 Zhejiang, China.
Zhou X; Institute of Drug Discovery Technology, Ningbo University, 315211 Zhejiang, China.
Wu J; Institute of Drug Discovery Technology, Ningbo University, 315211 Zhejiang, China.; Qian Xuesen Collaborative Research Center of Astrochemistry and Space Life Sciences, Ningbo University, 315211 Zhejiang, China.
Zhao Y; Institute of Drug Discovery Technology, Ningbo University, 315211 Zhejiang, China.; Qian Xuesen Collaborative Research Center of Astrochemistry and Space Life Sciences, Ningbo University, 315211 Zhejiang, China.
Pokaż więcej
Źródło:
The Journal of organic chemistry [J Org Chem] 2022 Dec 02; Vol. 87 (23), pp. 16106-16110. Date of Electronic Publication: 2022 Nov 16.
Typ publikacji:
Journal Article
MeSH Terms:
Manganese*
Indoles*
Catalysis ; Oxidation-Reduction
Czasopismo naukowe
Tytuł:
Nec-1 alleviated the deleterious effect of CoCl 2 on C2C12 myoblast differentiation and fusion via the mTOR pathway.
Autorzy:
Chen J; Department of Health Management Center, Guangdong Second Provincial General Hospital, 466 Xin Gang Zhong Road, Guangzhou 510317, China.
She Y; Guangdong Traditional Medical and Sports Injury Rehabilitation Research Institute, Guangdong Second Provincial General Hospital, 466 Xin Gang Zhong Road, Guangzhou 510317, China.
Chen R; Guangdong Traditional Medical and Sports Injury Rehabilitation Research Institute, Guangdong Second Provincial General Hospital, 466 Xin Gang Zhong Road, Guangzhou 510317, China. Electronic address: .
Shi H; Guangdong Traditional Medical and Sports Injury Rehabilitation Research Institute, Guangdong Second Provincial General Hospital, 466 Xin Gang Zhong Road, Guangzhou 510317, China.
Lei S; Guangdong Traditional Medical and Sports Injury Rehabilitation Research Institute, Guangdong Second Provincial General Hospital, 466 Xin Gang Zhong Road, Guangzhou 510317, China.
Zhou S; Guangdong Traditional Medical and Sports Injury Rehabilitation Research Institute, Guangdong Second Provincial General Hospital, 466 Xin Gang Zhong Road, Guangzhou 510317, China.
Pokaż więcej
Źródło:
Tissue & cell [Tissue Cell] 2022 Dec; Vol. 79, pp. 101910. Date of Electronic Publication: 2022 Aug 31.
Typ publikacji:
Journal Article
MeSH Terms:
Muscle Development*
TOR Serine-Threonine Kinases*
Indoles*/pharmacology
Imidazoles*/pharmacology
Animals ; Mice ; Cell Differentiation ; Myoblasts
Czasopismo naukowe
Tytuł:
Recent developments in green approaches for sustainable synthesis of indole-derived scaffolds.
Autorzy:
Nasri S; Department of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Iran.
Bayat M; Department of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Iran. bayat_.
Miankooshki FR; Department of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Iran.
Samet NH; Department of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Iran.
Pokaż więcej
Źródło:
Molecular diversity [Mol Divers] 2022 Dec; Vol. 26 (6), pp. 3411-3445. Date of Electronic Publication: 2022 Jan 15.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Indoles*/chemistry
Heterocyclic Compounds*
Catalysis ; Solvents
Czasopismo naukowe
Tytuł:
A Rh(II)-catalyzed highly stereoselective [3 + 2] annulation of vinyl diazoacetates with indole-2-carbaldehyde for the synthesis of indolyl dihydrofurans.
Autorzy:
Zheng R; Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Xu A; Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Huang J; Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Zhang Z; Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Yin X; Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Zhang T; Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Hu W; Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Qian Y; Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China. .
Pokaż więcej
Źródło:
Molecular diversity [Mol Divers] 2022 Dec; Vol. 26 (6), pp. 3379-3386. Date of Electronic Publication: 2022 Jan 20.
Typ publikacji:
Journal Article
MeSH Terms:
Indoles*
Aldehydes*
Stereoisomerism ; Catalysis ; Cycloaddition Reaction
Czasopismo naukowe
Tytuł:
Rh(II)-catalyzed Doyle-Kirmse reaction: access to unprotected 3-allyl/3-allenyl-3-(thio)oxindoles.
Autorzy:
Lu X; School of Chemistry and Chemical Engineering, Laboratory of Marine Green Fine Chemicals, Lingnan Normal University, Zhanjiang, 524048, P. R. China. .
Yang K; School of Chemistry and Chemical Engineering, Laboratory of Marine Green Fine Chemicals, Lingnan Normal University, Zhanjiang, 524048, P. R. China. .
Xu X; School of Chemistry and Chemical Engineering, Laboratory of Marine Green Fine Chemicals, Lingnan Normal University, Zhanjiang, 524048, P. R. China. .
Sun S; Qiqihar Medical University, Qiqihar, 161006, P. R. China.
Feng S; School of Chemistry and Chemical Engineering, Laboratory of Marine Green Fine Chemicals, Lingnan Normal University, Zhanjiang, 524048, P. R. China. .
Bashir MA; Peking University ShenZhen Graduate School, Shenzhen, 518055, P. R. China.
Liang F; School of Chemistry and Chemical Engineering, Laboratory of Marine Green Fine Chemicals, Lingnan Normal University, Zhanjiang, 524048, P. R. China. .
Lin J; School of Chemistry and Chemical Engineering, Laboratory of Marine Green Fine Chemicals, Lingnan Normal University, Zhanjiang, 524048, P. R. China. .
Huang G; School of Chemistry and Chemical Engineering, Laboratory of Marine Green Fine Chemicals, Lingnan Normal University, Zhanjiang, 524048, P. R. China. .
Pokaż więcej
Źródło:
Organic & biomolecular chemistry [Org Biomol Chem] 2022 Nov 30; Vol. 20 (46), pp. 9228-9233. Date of Electronic Publication: 2022 Nov 30.
Typ publikacji:
Journal Article
MeSH Terms:
Indoles*
Oxindoles ; Stereoisomerism ; Molecular Structure ; Catalysis
Czasopismo naukowe
Tytuł:
Visible-Light-Induced C-F Bond Activation for the Difluoroalkylation of Indoles.
Autorzy:
Shreiber ST; Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
Granados A; Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
Matsuo B; Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
Majhi J; Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
Campbell MW; Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
Patel S; Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
Molander GA; Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
Pokaż więcej
Źródło:
Organic letters [Org Lett] 2022 Nov 25; Vol. 24 (46), pp. 8542-8546. Date of Electronic Publication: 2022 Nov 14.
Typ publikacji:
Journal Article
MeSH Terms:
Indoles*/chemistry
Hydrocarbons, Fluorinated*
Catalysis ; Oxidation-Reduction
Czasopismo naukowe
Tytuł:
One-Step Synthesis of Hydropyrrolo[3,2- b ]indoles via Cascade Reactions of Oxindole-Derived Nitrones with Allenoates.
Autorzy:
Luo ML; State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, P. R. China.
Hou Q; State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, P. R. China.
Liu SJ; State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, P. R. China.
Zhao Q; State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, P. R. China.
Qin R; State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, P. R. China.
Peng C; State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, P. R. China.
Han B; State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, P. R. China.
Zhan G; State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, P. R. China.
Pokaż więcej
Źródło:
Organic letters [Org Lett] 2022 Nov 25; Vol. 24 (46), pp. 8493-8497. Date of Electronic Publication: 2022 Nov 10.
Typ publikacji:
Journal Article
MeSH Terms:
Indoles*/chemistry
Nitrogen Oxides*
Oxindoles ; Catalysis
Czasopismo naukowe
Tytuł:
Polymethine Molecular Platform for Ratiometric Fluorescent Probes in the Second near-Infrared Window.
Autorzy:
Lan Q; Key Laboratory of Smart Drug Delivery, Ministry of Education, School of Pharmacy, Fudan University, Zhangheng Road 826, Shanghai 201203, China.; Department of Chemistry, State Key Laboratory of Molecular Engineering of Polymers, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials and iChem, Fudan University, Shanghai 200433, China.
Yu P; Department of Chemistry, State Key Laboratory of Molecular Engineering of Polymers, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials and iChem, Fudan University, Shanghai 200433, China.
Yan K; Department of Chemistry, State Key Laboratory of Molecular Engineering of Polymers, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials and iChem, Fudan University, Shanghai 200433, China.
Li X; Department of Chemistry, State Key Laboratory of Molecular Engineering of Polymers, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials and iChem, Fudan University, Shanghai 200433, China.
Zhang F; Department of Chemistry, State Key Laboratory of Molecular Engineering of Polymers, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials and iChem, Fudan University, Shanghai 200433, China.
Lei Z; Key Laboratory of Smart Drug Delivery, Ministry of Education, School of Pharmacy, Fudan University, Zhangheng Road 826, Shanghai 201203, China.
Pokaż więcej
Źródło:
Journal of the American Chemical Society [J Am Chem Soc] 2022 Nov 23; Vol. 144 (46), pp. 21010-21015. Date of Electronic Publication: 2022 Oct 25.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Fluorescent Dyes*
Indoles*
Fluorescence
Czasopismo naukowe
Tytuł:
Oxidative two-way regiocontrolled coupling of 3-methoxycarbonylcatechol and indoles to arylindoles.
Autorzy:
Sawama Y; Graduate School of Pharmaceutical Sciences, Osaka University, 1-6, Yamada-oka, Suita, Osaka 565-0871, Japan. .
Kuwata S; A Laboratory of Organic Chemistry, Gifu Pharmaceutical University, 1-25-4-Daigaku-nishi, Gifu 501-1196, Japan.
Mae M; Graduate School of Pharmaceutical Sciences, Osaka University, 1-6, Yamada-oka, Suita, Osaka 565-0871, Japan. .
Udagawa T; Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan.
Akai S; Graduate School of Pharmaceutical Sciences, Osaka University, 1-6, Yamada-oka, Suita, Osaka 565-0871, Japan. .
Sajiki H; A Laboratory of Organic Chemistry, Gifu Pharmaceutical University, 1-25-4-Daigaku-nishi, Gifu 501-1196, Japan.
Pokaż więcej
Źródło:
Chemical communications (Cambridge, England) [Chem Commun (Camb)] 2022 Nov 22; Vol. 58 (93), pp. 12935-12938. Date of Electronic Publication: 2022 Nov 22.
Typ publikacji:
Journal Article
MeSH Terms:
Indoles*
Oxidative Stress*
Oxidation-Reduction
Czasopismo naukowe
Tytuł:
Catalytic Vilsmeier-Haack Reactions for C1-Deuterated Formylation of Indoles.
Autorzy:
Xue J; Center of Basic Molecular Science (CBMS), Department of Chemistry, Tsinghua University, Beijing 100084, China.
Zhang YS; Center of Basic Molecular Science (CBMS), Department of Chemistry, Tsinghua University, Beijing 100084, China.
Huan Z; Center of Basic Molecular Science (CBMS), Department of Chemistry, Tsinghua University, Beijing 100084, China.
Yang JD; Center of Basic Molecular Science (CBMS), Department of Chemistry, Tsinghua University, Beijing 100084, China.
Cheng JP; Center of Basic Molecular Science (CBMS), Department of Chemistry, Tsinghua University, Beijing 100084, China.; State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.; Haihe Laboratory of Sustainable Chemical Transformations, Keyan West Road, Tianjin 300192, China.
Pokaż więcej
Źródło:
The Journal of organic chemistry [J Org Chem] 2022 Nov 18; Vol. 87 (22), pp. 15539-15546. Date of Electronic Publication: 2022 Nov 08.
Typ publikacji:
Journal Article
MeSH Terms:
Indoles*
Catalysis
Czasopismo naukowe
Tytuł:
Selective Construction of All-Carbon Quaternary Centers via Relay Catalysis of Indole C-H Functionalization/Allylic Alkylation.
Autorzy:
Zhang J; College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, 333 Longteng Road, Shanghai 201620, China.; State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
Lu B; State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
Ge Z; State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
Wang L; College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, 333 Longteng Road, Shanghai 201620, China.
Wang X; State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.; School of Chemistry and Materials Science, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, 1 Sub-lane Xiangshan, Hangzhou 310024, China.
Pokaż więcej
Źródło:
Organic letters [Org Lett] 2022 Nov 18; Vol. 24 (45), pp. 8423-8428. Date of Electronic Publication: 2022 Nov 04.
Typ publikacji:
Journal Article
MeSH Terms:
Carbon*
Indoles*
Stereoisomerism ; Molecular Structure ; Catalysis ; Alkylation
Czasopismo naukowe
Tytuł:
Diastereoselective Access to Triazolo[1,2- a ]indolines via a Bio-Inspired Oxidative Cyclization of NH-Indoles.
Autorzy:
Yu L; School of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing312000, China.
Huang S; School of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing312000, China.
Cai T; Zhejiang Engineering Research Center of Fat-Soluble Vitamin, Shaoxing312000, China.
Du K; School of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing312000, China.
Wu C; School of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing312000, China.
Dong H; School of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing312000, China.
Shen R; Zhejiang Engineering Research Center of Fat-Soluble Vitamin, Shaoxing312000, China.
Pokaż więcej
Źródło:
The Journal of organic chemistry [J Org Chem] 2022 Nov 18; Vol. 87 (22), pp. 15114-15119. Date of Electronic Publication: 2022 Oct 06.
Typ publikacji:
Journal Article
MeSH Terms:
Indoles*/chemistry
Imines*
Cyclization ; Oxidation-Reduction ; Oxidative Stress ; Catalysis
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

Prześlij opinię

Twoje opinie są dla nas bardzo ważne i mogą być niezwykle pomocne w pokazaniu nam, gdzie możemy dokonać ulepszeń. Bylibyśmy bardzo wdzięczni za poświęcenie kilku chwil na wypełnienie krótkiego formularza.

Formularz