المؤلفون: Kavita Kumari Meena, Kamal Kant Serawat, R K Gunsaria

المصدر: Indian Journal of Science and Technology, 16(42), 3721-3726, (2023-11-12)

مصطلحات موضوعية: Schiff Base, N'­bis(2­hydroxy­3­methoxybenzaldehyde)­2­phenyl­1, 3­propanediamine, Antifungal, Candidiasis, Candida

Relation: eissn:0974-5645; https://doi.org/10.17485/IJST/v16i42.369; oai:zenodo.org:13674879

الاتاحة: https://doi.org/10.17485/IJST/v16i42.369
https://indjst.org/articles/in-vitro-evaluation-of-antifungal-activity-of-synthesized-novel-znii-complex-with-schiff-base-ligand

المؤلفون: Pokharkar, O., Zyryanov, G. V., Tsurkan, M. V.

المصدر: Microbiology Research

مصطلحات موضوعية: 3CLPRO, ANTIVIRAL, MPRO, MARINE DRUGS, NATURAL PRODUCTS, PLPRO, REPURPOSING, S. ARENICOLA, S. PACIFICA, S. TROPICA, SALINISPORA, SARS-COV-2, 27 O DEMETHYL 25 O DESACETYLRIFAMYCIN, 3 AMINO 2 METHYL N (1R)-1 (NAPHTHALEN 1 YL) ETHYL BENZAMIDE, 7 TRIHYDROXY 2 PHENYL 4H CHROMEN 4 ONE, ANTIPROTEALIDE, ARENAMIDE A, ARENAMIDE B, ARENAMIDE C, CORONAVIRUS 3C PROTEASE, CYCLOMARAZINE A, CYCLOMARIN A, CYCLOMARIN D, DEFEROXAMINE, EMERICELLAMIDE, IKARUGAMYCIN, LOMAIVITICIN, LOMAIVITICIN A, LOMAIVITICIN D, LOMAIVITICIN E

وصف الملف: application/pdf

Relation: Pokharkar, O, Zyryanov, G & Tsurkan, M 2023, 'Natural Products from Marine Actinomycete Genus Salinispora Might Inhibit 3CLpro and PLpro Proteins of SARS-CoV-2: An In Silico Evidence', Microbiology Research, Том. 14, № 4, стр. 1907-1941. https://doi.org/10.3390/microbiolres14040130; Pokharkar, O., Zyryanov, G., & Tsurkan, M. (2023). Natural Products from Marine Actinomycete Genus Salinispora Might Inhibit 3CLpro and PLpro Proteins of SARS-CoV-2: An In Silico Evidence. Microbiology Research, 14(4), 1907-1941. https://doi.org/10.3390/microbiolres14040130; Final; All Open Access, Gold; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85180651227&doi=10.3390%2fmicrobiolres14040130&partnerID=40&md5=de82556cb5df0f0ea91eff8ff9536e0d; https://www.mdpi.com/2036-7481/14/4/130/pdf?version=1700042435; http://elar.urfu.ru/handle/10995/131079; 85180651227; 001132291400001

الاتاحة: http://elar.urfu.ru/handle/10995/131079
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85180651227&doi=10.3390%2fmicrobiolres14040130&partnerID=40&md5=de82556cb5df0f0ea91eff8ff9536e0d
https://www.mdpi.com/2036-7481/14/4/130/pdf?version=1700042435
https://doi.org/10.3390/microbiolres14040130

المؤلفون: Ahanthem Priyanca Devi, Naveen Dhingra, Uma Bhardwaj, R.S. Chundawat, Chetan K. Joshi, Shivendra Singh, Keshav Lalit Ameta

المصدر: Current Research in Green and Sustainable Chemistry, Vol 5, Iss , Pp 100234- (2022)

مصطلحات موضوعية: Chalcones, 2-(phenyl)-4H-chromen-4-ones, Antifungal activity, Molecular docking, Chitinase, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2666086521001818; https://doaj.org/toc/2666-0865

URL الوصول: https://doaj.org/article/9eb13e18971d4c4991b1d639a38b107f

المؤلفون: Lenka Loukotová (5047283), Pavel Švec (9728612), Ondřej Groborz (9728627), Tomáš Heizer (11200059), Hynek Beneš (3993560), Helena Raabová (11200062), Tereza Bělinová (11200065), Vít Herynek (2180164), Martin Hrubý (2264950)

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Molecular Biology, Neuroscience, Pharmacology, Biotechnology, Mental Health, Space Science, Chemical Sciences not elsewhere classified, PhOx, grad, PMeOx 70, gradient, drug loading capacity, glass transition intervals, monomer, Analogous Amphiphilic Gradient, 2- methyl -2-oxazoline, 2- phenyl -2-oxazoline, block analogs, BuPhOx, drug delivery systems, block copolymers

Relation: https://figshare.com/articles/journal_contribution/Direct_Comparison_of_Analogous_Amphiphilic_Gradient_and_Block_Polyoxazolines/15071034

الاتاحة: https://doi.org/10.1021/acs.macromol.0c02674.s001

المؤلفون: Caifa You (10427035), Xue-Qi Wang (8739744), Xiuwen Zhou (460008), Yi Yuan (180239), Liang-Sheng Liao (1586392), Yu-Chan Liao (11241543), Pi-Tai Chou (1282068), Yun Chi (1483534)

مصطلحات موضوعية: Biochemistry, Microbiology, Molecular Biology, Neuroscience, Physiology, Biotechnology, Marine Biology, Computational Biology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, withdrawing trifluoromethyl substitution, terminal emitter afforded, synthesized two series, ray diffraction studies, phosphorescent organic light, oled device based, heterocyclic carbene fragment, external quantum efficiency, degassed thf solution, 8 – 42, photoluminescence quantum yields, photoluminescence peak wavelengths, ∼ 420 nm, 2 ‑ phenyl, significantly improved max, phosphors bearing 1, 2 , max , peak max

Relation: https://figshare.com/articles/journal_contribution/Homoleptic_Ir_III_Phosphors_with_2_Phenyl-1_2_4-triazol-3-ylidene_Chelates_for_Efficient_Blue_Organic_Light-Emitting_Diodes/17128378

الاتاحة: https://doi.org/10.1021/acsami.1c17308.s001

المؤلفون: Marcin Drop (6541334), Vittorio Canale (2606626), Séverine Chaumont-Dubel (10291045), Rafał Kurczab (1312479), Grzegorz Satała (805228), Xavier Bantreil (1887601), Maria Walczak (6051134), Paulina Koczurkiewicz-Adamczyk (9981364), Gniewomir Latacz (1570159), Anna Gwizdak (10291048), Martyna Krawczyk (6541325), Joanna Gołębiowska (10291051), Katarzyna Grychowska (2658958), Andrzej J. Bojarski (499184), Agnieszka Nikiforuk (420161), Gilles Subra (1494619), Jean Martinez (150107), Maciej Pawłowski (1792099), Piotr Popik (292215), Philippe Marin (460346), Frédéric Lamaty (1498096), Paweł Zajdel (2606617)

مصطلحات موضوعية: Biochemistry, Neuroscience, Physiology, Pharmacology, Mental Health, Infectious Diseases, Chemical Sciences not elsewhere classified, 5- HT 6 R-operated, scopolamine-induced memory decline, pyrrole -3-carboxamide, canonical indole-like skeleton, novel object recognition test, memory impairment paradigms, 2- phenyl, 5- HT 6 R, attentional set-shifting task

Relation: https://figshare.com/articles/journal_contribution/2_Phenyl_1_i_H_i_pyrrole-3-carboxamide_as_a_New_Scaffold_for_Developing_5_HT_sub_6_sub_Receptor_Inverse_Agonists_with_Cognition-Enhancing_Activity/14199994

الاتاحة: https://doi.org/10.1021/acschemneuro.1c00061.s001

المؤلفون: Arslan, Åževki, Çetin, DoÄŸan, KonuÅŸ, Metin, Kurt KızıldoÄŸan, Aslıhan, Otur, ÇiÄŸdem, Yılmaz, Can, Mutlu, DoÄŸukan, Kıvrak, Arif, Algso, Muheb, Kayhan, Abdussamet

مصطلحات موضوعية: Antimicrobial, Antioxidant, Cytotoxicity, Heteroaromatic compounds, Indole, Small molecules, 1 ethyl 2 phenyl 3 phenylethyl 3 thiophen 2 yl 1h indole derivative, antiinfective agent, indole derivative, unclassified drug, antimicrobial activity, antioxidant activity, Article, cancer cell line, controlled study, drug structure, drug synthesis, enzyme activity, Hep-G2 cell line, human, human cell, MTT assay, Sonogashira reaction, cytotoxic agent, glutathione transferase

Relation: Letters in Drug Design and Discovery; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://doi.org/10.2174/1570180817999201109203226; https://hdl.handle.net/11499/47690; 18; 461; 470

الاتاحة: https://hdl.handle.net/11499/47690
https://doi.org/10.2174/1570180817999201109203226

المؤلفون: Yulia A. Trukhanova, Denis A. Kolesnik, Elena V. Kuvaeva, Galina V. Ksenofontova, Marina V. Sopova, Igor P. Yakovlev

المصدر: Chemistry Proceedings; Volume 8; Issue 1; Pages: 99

مصطلحات موضوعية: isoindoline-1,3-diones, 2-(phenyl(phenylimino)methyl)isoindoline-1,3-dione, analgesic activity, N -substituted derivatives of phthalimide, non-steroidal analgesic

وصف الملف: application/pdf

Relation: https://dx.doi.org/10.3390/ecsoc-25-11773

الاتاحة: https://doi.org/10.3390/ecsoc-25-11773

المؤلفون: Sala E., Ferrari F., Lanza M., Milia C., Sabatini C., Bonazzi A., Comi E., Borsi Franchini M., Caselli G., Rovati L. C.

المساهمون: Sala, E, Ferrari, F, Lanza, M, Milia, C, Sabatini, C, Bonazzi, A, Comi, E, Borsi Franchini, M, Caselli, G, Rovati, L

مصطلحات موضوعية: 2 phenyl 6 (1h imidazol 1 yl)quinazoline, analgesic agent, cr 4056, morphine, mu opiate receptor, naloxone, quinazoline derivative, unclassified drug

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/32154915; info:eu-repo/semantics/altIdentifier/wos/WOS:000527951300001; volume:177; issue:14; firstpage:3291; lastpage:3308; numberofpages:18; journal:BRITISH JOURNAL OF PHARMACOLOGY; https://hdl.handle.net/10281/494263; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85084144839

الاتاحة: https://hdl.handle.net/10281/494263
https://doi.org/10.1111/bph.15049

المؤلفون: Kılıç, Zeynel, Hayvalı, Zeliha

المساهمون: Dil ve Tarih-Coğrafya Fakültesi

مصطلحات موضوعية: 1,5 dimethyl 2 phenyl 1,2 dihydro 3h pyrazol 3 one 4 (1 aminomethylidenyl) 5' hydroxybenzo 15 crown 5benzo 15 crown 5 derivativ

وصف الملف: application/pdf

Relation: Analytical Sciences; Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı; 1,5 dimethyl 2 phenyl 1,2 dihydro 3h pyrazol 3 one 4 (1 aminomethylidenyl) 5' hydroxybenzo 15 crown 5benzo 15 crown 5 derivativ; https://doi.org/10.2116/analsci.18.495; http://hdl.handle.net/20.500.12575/69521; 18; 495; 496

الاتاحة: https://doi.org/10.2116/analsci.18.495
https://hdl.handle.net/20.500.12575/69521

المؤلفون: Oleksii M. ANTYPENKO, Sergiy I. KOVALENKO, Galina О. ZHERNOVA

المصدر: Scientia Pharmaceutica; Volume 84; Issue 2; Pages: 233-254

مصطلحات موضوعية: 1-[2-(1 H -Tetrazol-5-yl)-R 1 -phenyl]-3-R 2 -phenyl(ethyl)ureas, Cyclization, Hypoglycemic activity, Molecular docking, Synthesis

وصف الملف: application/pdf

Relation: https://dx.doi.org/10.3797/scipharm.1507-14

الاتاحة: https://doi.org/10.3797/scipharm.1507-14

المؤلفون: Can Yilmaz, Arif Kivrak, Sevki Arslan, Abdussamet Kayhan, Dogukan Mutlu, Muheb A. S. Algso, Çiğdem Otur, Aslıhan Kurt-Kızıldoğan, Metin Konus, Doğan Çetin

المساهمون: [Belirlenecek]

مصطلحات موضوعية: Antioxidant, antioxidant, medicine.medical_treatment, antioxidant activity, Pharmaceutical Science, Hep-G2 cell line, Article, 1 ethyl 2 phenyl 3 phenylethyl 3 thiophen 2 yl 1h indole derivative, glutathione transferase, Drug Discovery, medicine, controlled study, human, indole derivative, Cytotoxicity, Indole test, antimicrobial activity, MTT assay, Chemistry, human cell, Antimicrobial, Small molecule, unclassified drug, enzyme activity, antiinfective agent, heteroaromatic compounds, drug structure, small molecules, Biochemistry, Indole, cytotoxic agent, drug synthesis, Molecular Medicine, cytotoxicity, antimicrobial, Sonogashira reaction, cancer cell line

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::424014426a972ede90d853bbf84018da
https://hdl.handle.net/11491/7477

المؤلفون: Martins Alho, M.A., Moglioni, A.G., Brousse, B., Moltrasio, G.Y., D'Accorso, N.B.

المصدر: Arkivoc 2000;2000(4 SPECISS):627-640

مصطلحات موضوعية: 3,4 dihydronaphthalen 1(2h) one thiosemicarbazone, 3,4' dimethoxybenzophenone thiocarbamazone, 4 methoxybenzophenone thiocarbamazone, 4,4' dimethoxybenzophenone thiocarbamazone, 5 acetamido 3 n acetyl 2 (3',4' dimethoxyphenyl) 2 phenyl 1,3,4 thiadiazoline, 5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1,3,4 thiadiazoline, 5 acetamido 3 n acetyl 2,2 bis(4' methoxyphenyl) 1,3,4 thiadiazoline, 5 acetamido 3 n acetyl 2,2 diphenyl 1,3 thiadiazoline, 5 methoxyindan 1 one thiosemicarbazone, 6 methoxyindan 1 one thiosemicarbazone, anthrone thiosemicarbazone, antifungal agent, antiinfective agent, heterocyclic compound, hydrogen, indan 1 one thiosemicarbazone, ketone derivative, spiro[5 acetamido 3 n acetyl 2,1' (1',2',3',4' tetrahydronaphthalen)], 1,3,4 thiadiazoline, spiro[5 acetamido 3 n acetyl 2,1' (5' methoxyindan)], spiro[5 acetamido 3 n acetyl 2,1' (6' methoxyindan)], spiro[5 acetamido 3 n acetyl 2,1' indane], thiadiazole derivative, thiosemicarbazone derivative, unclassified drug, carbon nuclear magnetic resonance, chemical structure, conference paper, drug synthesis, mass spectrometry

وصف الملف: application/pdf

Relation: http://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho; http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2000_n4SPECISS_p627_MartinsAlho_oai

الاتاحة: https://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2000_n4SPECISS_p627_MartinsAlho_oai

المؤلفون: Szabó K.E., Kyriakis E., Psarra A.-M.G., Karra A.G., Sipos Á., Docsa T., Stravodimos G.A., Katsidou E., Skamnaki V.T., Liggri P.G.V., Zographos S.E., Mándi A., Király S.B., Kurtán T., Leonidas D.D., Somsák L.

المصدر: Journal of Medicinal Chemistry ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85069627561&doi=10.1021%2facs.jmedchem.9b00356&partnerID=40&md5=d7ab0ac44b9677c5d2be42dcb5f9f252

مصطلحات موضوعية: 1',5 anhydro 2',3',4',6' tetra o benzoyl dextro glucitol spiro(1',5] 2 (1 naphthyl) imidazolin 4 one, 1',5 anhydro 2',3',4',6' tetra o benzoyl dextro glucitol spiro(1',5] 2 (2 naphthyl) imidazolin 4 one, 1',5 anhydro 2',3',4',6' tetra o benzoyl dextro glucitol spiro(1',5] 2 (4 trifluoromethylphenyl) imidazolin 4 one, 1',5 anhydro 2',3',4',6' tetra o benzoyl dextro glucitol spiro(1',5] 2 phenyl imidazolin 4 one, 1',5' anhydro 2',3',4',6' tetra o benzoyl dextro glucitol spiro[1',5] 2 (1 naphthyl) imidazolin 4 one, 1',5' anhydro 2',3',4',6' tetra o benzoyl dextro glucitol spiro[1',5] 2 (2 naphthyl) imidazolin 4 one, 1',5' anhydro 2',3',4',6' tetra o benzoyl dextro glucitol spiro[1',5] 2 (4 trifluoromethylphenyl) imidazolin 4 one, 1',5' anhydro 2',3',4',6' tetra o benzoyl dextro glucitol spiro[1',5] 2 phenyl imidazolin 4 one, 1',5' anhydro dextro glucitol spiro [1',5] 2 (1 naphthyl) imidazolin 4 one, 1',5' anhydro dextro glucitol spiro [1',5] 2 (1 naphthyl)imidazolin 4 one, 1',5' anhydro dextro glucitol spiro [1',5] 2 (2 naphthyl) imidazolin 4 one, 1',5' anhydro dextro glucitol spiro [1',5] 2 (2 naphthyl)imidazolin 4 one, 1',5' anhydro dextro glucitol spiro [1',5] 2 (4 trifluoromethylphenyl) imidazolin 4 one, 1',5' anhydro dextro glucitol spiro [1',5] 2 (4 trifluoromethylphenyl)imidazolin 4 one, 1',5' anhydro dextro glucitol spiro [1',5] 2 phenyl imidazolin 4 one, c (2,3,4,6 tetra o benzoyl 1 benzylideneamino 1 alpha dextro deoxy glucopyranosyl)formamide, c (2,3,4,6 tetra o benzoyl 1 benzylidenetriazenyl 1 alpha dextro deoxy glucopyranosyl)formamide, c (2,3,4,6 tetra o benzoyl 1 deoxy beta dextro glucopyranosyl)formamide, c [2,3,4,6 tetra o benzoyl 1 deoxy 1 (4 trifluoromethylbenzylidene)amino beta dextro glucopyranosyl]formamide, c [2,3,4,6 tetra o benzoyl 1 deoxy 1 (naphth 1 ylmethylidene)amino alpha dextro glucopyranosyl]formamide, c [2,3,4,6 tetra o benzoyl 1 deoxy 1 (naphth 1 ylmethylidene)amino beta dextro glucopyranosyl]formamide, c [2,3,4,6 tetra o benzoyl 1 deoxy 1 (naphth 2 ylmethylidene)amino alpha dextro glucopyranosyl]formamide, c [2,3,4,6 tetra o benzoyl 1 deoxy 1 (naphth 2 ylmethylidene)amino beta dextro glucopyranosyl]formamide, c [2,3,4,6 tetra o benzoyl 1 deoxy 1(4 trifluoromethylbenzylidene)amino alpha dextro glucopyranosyl]formamide, glycogen phosphorylase, glycosyltransferase inhibitor, imidazoline derivative, spiro compound, unclassified drug, enzyme inhibitor

Relation: http://hdl.handle.net/11615/79566

الاتاحة: http://hdl.handle.net/11615/79566
https://doi.org/10.1021/acs.jmedchem.9b00356

المؤلفون: Pavan Kumar Mandali, Dillip Kumar Chand

المصدر: Synthesis. 47:1661-1668

مصطلحات موضوعية: 4 (benzofuran 2 yl)butan 1 ol, Sonogashira cross-coupling reaction, Nanoparticle, Catalyzed synthesis, methyl 2 (4 bromophenyl)benzofuran 5 carboxylate, Chemical reaction, Domino, Cascade reaction, domino reaction, Chemical reactions, 2 [3 (trifluoromethyl)phenyl]benzofuran, Organic chemistry, Reaction kinetics, Catalysts, 2 (2,4 difluorophenyl)benzofuran, Chemistry, 2 (3 pyridyl)benzofuran, methyl 2 octylbenzofuran 5 carboxylate, nanop palladium nanop unclassified drug, 2 phenylbenzofuran, methyl 2 (4 hydroxybutyl)benzofuran 5 carboxylate, One-pot synthesis, 2 octylbenzofuran, 2 (4 tolyl)benzofuran, reaction analysis, methyl 2 phenylbenzofuran 5 carboxylate, Synthesis (chemical), benzofuran derivative, Domino reactions, 2 (4 bromophenyl)benzofuran, 4 (benzofuran 2 yl)benzonitrile, Palladium, 2 [3 [(4 methoxyphenyl)ethynyl]phenyl]benzofuran, chemical reaction, 2 (4 tert butylphenyl)benzofuran, 2 phenyl 3 (phenylethynyl)benzofuran, Sonogashira coupling, chemistry.chemical_element, one pot synthesis, methyl 2 (4 cyanophenyl)benzofuran 5 carboxylate, Catalysis, 2 (2 tolyl)benzofuran, methyl 2 [3 (benzofuran 2 yl)phenyl]benzofuran 5 carboxylate, unindexed drug, physical chemistry, 2 (3 ethynylphenyl)benzofuran, methyl 2 butylbenzofuran 5 carboxylate, 2 (3 aminophenyl)benzofuran, 2 (3 tolyl)benzofuran, Benzofurans, Organic Chemistry, Palladium nanoparticles, Nanostructures, drug structure, 1,3 di(benzofuran 2 yl)benzene, Cross-couplings, 2 butylbenzofuran, Nanoparticles, drug synthesis, Sonogashira reaction, Ambient conditions, 2 (4 aminophenyl)benzofuran

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f031e85c202bb821de9682d799a97bf
https://doi.org/10.1055/s-0034-1380463

المؤلفون: Koutentis, Panayiotis Andreas, Loizou, G., Lo Re, D.

المساهمون: Koutentis, Panayiotis Andreas [0000-0002-4652-7567]

المصدر: Journal of Organic Chemistry
J.Org.Chem.

مصطلحات موضوعية: Non-oxidative, cross linking, synthesis, Intramolecular reaction, Stereochemistry, chemistry.chemical_element, nucleophilicity, 5 (diethylamino) 2 phenyl 6h[1,2,4]triazino[ 5,6,1 jk]carbazol 6 one, 8,10 dihydro 1 iodo 10 phenylphenazin 2(7h)one, Cyclizations, Ring (chemistry), Chemical synthesis, Nitrogen compounds, Catalysis, Addition reactions, fluoranthene, Fluorides, 5 methoxy 2 phenyl 6h[1,2,4]triazino[5,6,1 jk]carbazol 6 one, Regioselective nucleophilic addition, Metabolites, Organometallic Compounds, silver, oxidation reduction potential, Aza Compounds, Nucleophilic addition, Molecular Structure, 2 phenyl 5 (pyrrolidin 1 yl) 6h[1,2,4]triazino[ 5,6,1 jk]carbazol 6 one, Methoxy, Organic Chemistry, article, Ring systems, Silver Compounds, Regioselectivity, Stereoisomerism, palladium, Silver halides, unclassified drug, 2 phenyl 5 (phenylthio) 6h[1,2,4]triazino[ 5,6,1 jk]carbazol 6 one, drug structure, chemistry, Cyclization, Intramolecular force, Oxidation-Reduction, Palladium

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e97eb6cab863b5b3b5daa10b2475262
https://doi.org/10.1021/jo200966k

المؤلفون: D. J. C. Prasad, Govindasamy Sekar, E. A. Jaseer

المصدر: Tetrahedron. 66:2077-2082

مصطلحات موضوعية: 5 chloro 2 p tolyl benzo[b]furan, 2 (4 fluorophenyl)benzo[b]furan, 2-[3 (trifluoromethyl) phenyl] benzo[b]furan, Intramolecular reaction, 5 tert butyl 2 phenyl benzo[b]furan, Sonogashira coupling, chemistry.chemical_element, 4 chloro 2 iodophenol, Biochemistry, Medicinal chemistry, Coupling reaction, chemistry.chemical_compound, 5 chloro 2 (4 methoxyphenyl) benzofuran, Drug Discovery, 2 (4 pentyl phenyl) benzo[b]furan, 5 chloro 2 m tolyl benzo[b]furan, Benzofuran, methyl 4 (3 bromopropoxy)benzoate, 4 (3 bromopropoxy)benzoic acid, 5 chloro 2 phenyl benzo[b]furan, Chemistry, 4 (3 bromopropoxy)benzoyl chloride, Aryl, 2 p tolyl benzo[b]furan, Organic Chemistry, unclassified drug, 2 (4 methoxy phenyl) benzo[b]furan, 5 methyl 2 phenyl benzo[b]furan, 2 m tolyl benzo[b]furan, 5 chloro 2 (4 pentyl phenyl) benzo[b]furan, priority journal, 5 chloro 3 [4 (3 bromopropoxy)benzoyl] 2 (4 methoxyphenyl)benzofuran, Intramolecular force, benzofuran derivative, copper ion, drug synthesis, Phosphine, 5 chloro 3 [4 (3 diethylaminopropoxy)benzoyl] 2 (4 methoxyphenyl) benzofuran, Palladium

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1630eb5772fb58ac7a2f56684ca1764b
https://doi.org/10.1016/j.tet.2010.01.026

المؤلفون: M. A. Martins Alho, Beatriz N. Brousse, Albertina G. Moglioni, Norma D´Accorso, Graciela Y. Moltrasio

المصدر: ARKIVOC, Vol 2000, Iss 4, Pp 627-640 (2000)
Scopus-Elsevier
Arkivoc 2000;2000(4 SPECISS):627-640
Biblioteca Digital (UBA-FCEN)
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN

مصطلحات موضوعية: 5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1,3,4 thiadiazoline, Hydrogen, 5 methoxyindan 1 one thiosemicarbazone, Chemical structure, Heteroatom, 6 methoxyindan 1 one thiosemicarbazone, chemistry.chemical_element, spiro[5 acetamido 3 n acetyl 2,1' (5' methoxyindan)] 1,3,4 thiadiazoline, Mass spectrometry, proton nuclear magnetic resonance, 4 methoxybenzophenone thiocarbamazone, lcsh:QD241-441, lcsh:Organic chemistry, antifungal agent, thiosemicarbazone derivative, conference paper, mass spectrometry, heterocyclic compound, chemistry.chemical_classification, Antiinfective agent, 3,4' dimethoxybenzophenone thiocarbamazone, 5 acetamido 3 n acetyl 2 (3',4' dimethoxyphenyl) 2 phenyl 1,3,4 thiadiazoline, 4,4' dimethoxybenzophenone thiocarbamazone, Organic Chemistry, spiro[5 acetamido 3 n acetyl 2,1' (6' methoxyindan)] 1,3,4 thiadiazoline, ketone derivative, spiro[5 acetamido 3 n acetyl 2,1' (1',2',3',4' tetrahydronaphthalen)] 1,3,4 thiadiazoline, carbon nuclear magnetic resonance, Combinatorial chemistry, 5 acetamido 3 n acetyl 2,2 diphenyl 1,3 thiadiazoline, unclassified drug, Characterization (materials science), anthrone thiosemicarbazone, antiinfective agent, chemistry, Heterocyclic compound, hydrogen, 3,4 dihydronaphthalen 1(2h) one thiosemicarbazone, 5 acetamido 3 n acetyl 2,2 bis(4' methoxyphenyl) 1,3,4 thiadiazoline, indan 1 one thiosemicarbazone, chemical structure, Proton NMR, drug synthesis, thiadiazole derivative, spiro[5 acetamido 3 n acetyl 2,1' indane] 1,3,4 thiadiazoline

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7347c3859ba0ae4db3b74d756a439f6
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0001.413

المؤلفون: Berglund, Magnus, Dalence, Maria, Skogvall, Staffan, Sterner, Olov

المصدر: Bioorganic & Medicinal Chemistry. 16(5):2529-2540

مصطلحات موضوعية: Bronchodilator, SAR, 2-(Phenyl)ethyl, C-region, Thiourea, Capsazepine, Coupling region, Small human airways, Asthma, COPD, Naturvetenskap, Kemi, Organisk kemi, Natural Sciences, Chemical Sciences, Organic Chemistry

URL الوصول: https://lup.lub.lu.se/record/1042247
http://dx.doi.org/10.1016/j.bmc.2007.11.056

المؤلفون: Constantinou, Constantina, Papas, Konstantinos A., Constantinou, Andreas I.

المساهمون: Constantinou, Andreas I. [0000-0003-0365-1821]

المصدر: Current Cancer Drug Targets
Curr.Cancer Drug Targets

مصطلحات موضوعية: carcinoid, chm 1, cell organelle, vitamin D, Apoptosis, quinolone derivative, serine proteinase, Drug Discovery, advanced cancer, mitochondrion, Programmed cell death, Drug discovery, leukemia, clinical trial, Calpain, Cell biology, myeloma, Oncology, Caspases, calpain, signal transduction, protein Bax, receptor down regulation, Proteases, drug design, phenol derivative, caspase, 2' fluoro 6,7 methylenedioxy 2 phenyl 4 quinolone, Antineoplastic Agents, Necrosis, estradiol, unindexed drug, otorhinolaryngologic diseases, Humans, cathepsin, human, protein Bid, drug inhibition, apoptosis inducing factor, Pharmacology, drug targeting, rb 49, tumor resistance, protein phosphorylation, respiratory tract diseases, drug efficacy, herbaceous agent, paclitaxel poliglumex, flavopiridol, monoclonal antibody, molecular interaction, n methylpiperidinyl chlorophenyl flavone, solid tumor, benzyloxycarbonylvalylalanylaspartyl fluoromethyl ketone, mediator, Apoptosis Regulatory Proteins, Cancer Research, atiprimod, Mitochondrion, protein induction, AIF, Drug Delivery Systems, Caspase-independent cell death, oxidative stress, flavone derivative, bzl 101, receptor upregulation, antineoplastic agent, Caspase, AIF inhibitor, apoptosis inhibitor, Clinical Trials as Topic, biology, lung non small cell cancer, prostate cancer, unclassified drug, Mitochondria, cell death, cytotoxicity, rb 110, drug potency, Signal Transduction, liver cell carcinoma, animal structures, colecalciferol, regulatory mechanism, chromatin condensation, review, antineoplastic activity, tumor cell, Models, Biological, breast cancer, azaspirane, drug mechanism, Chemotherapy, Cathepsin, carcinogenic activity, nonhuman, 2,4,6 triiodophenol, cy 103, caspase inhibitor, gene expression, biology.protein, Cancer research, bobel 24, neoplasm, Peptide Hydrolases

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f95f44db4484ec1851baf66add766d4
https://doi.org/10.2174/156800909789271512