المؤلفون: Hasa, Dritan, Žakelj, Simon, Grabnar, Iztok, Cilurzo, Francesco, Dall'Acqua, Stefano, Riva, Antonella, Perissutti, Beatrice, Voinovich, Dario

المصدر: Pharmaceutics, vol. 12, no. 11, 1096, 2020.

مصطلحات موضوعية: tetraen, drug-in-adhesive patch, tetraene, lipofilni ekstrakt Echinacea angustifolia, prehod skozi kožo in vitro, udc:615.015, zdravilna učinkovina v adhezivnem obližu, pharmacokinetics, in vitro skin permeation, Echinacea angustifolia lipophilic extract

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https://hdl.handle.net/20.500.12556/RUL-134661

المؤلفون: Luís Gales, Michael Lee, José Alberto Pereira, Vitor Vasconcelos, Anake Kijjoa, Suradet Buttachon, Madalena Pinto, Ralph Urbatzka, Artur M. S. Silva, Tida Dethoup, Sara Freitas, Jidapa Noinart

المساهمون: CIIMAR - Centro Interdisciplinar de Investigação Marinha e Ambiental

المصدر: Marine Drugs; Volume 15; Issue 5; Pages: 139
Marine Drugs
Marine Drugs, Vol 15, Iss 5, p 139 (2017)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP

مصطلحات موضوعية: Models, Molecular, Aquatic Organisms, obesity, anti-obesity, Talaromyces, Ethyl acetate, Pharmaceutical Science, Anthraquinones, resveratrol, 01 natural sciences, emodin, Palmitic acid, chemistry.chemical_compound, citreorosein, Stylissa flabelliformis, Ergosterol, bis-anthraquinone, Drug Discovery, zebra fish, palmitic acid, lcsh:QH301-705.5, Pharmacology, Toxicology and Pharmaceutics (miscellaneous), Trichocomaceae, Citreorosein, ergosterol 5,8 endoperoxide, Molecular Structure, biology, sterol derivative, adult, stereochemistry, Porifera, unclassified drug, ergosta 4,6,8(14),22 tetraen 3 one, Secalonic acid, anthraquinone derivative, rheoemodin, crystal structure, questinol, Stereochemistry, animal experiment, embryo, talarosterone, Article, ergosterol derivatives, zebrafish Nile red assay, Animals, cyathisterone, controlled study, Talaromyces stipitatus, anthraquinones, secalonic acid A, 14. Life underwater, fallacinol, nonhuman, 010405 organic chemistry, X ray crystallography, biology.organism_classification, 0104 chemical sciences, 010404 medicinal & biomolecular chemistry, drug structure, lcsh:Biology (General), chemistry, sponge (Porifera), Anti-Obesity Agents, Emodin

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https://hdl.handle.net/10216/120500

المؤلفون: P.Ch. Chenchaiah, M. Vijaya Krishna, S. R. Ramadas

المصدر: Steroids. 40:519-533

مصطلحات موضوعية: heterocyclic steroid, Magnetic Resonance Spectroscopy, synthesis, Spectrophotometry, Infrared, 1,6 dithiabenz(3,4)estra 3,5(10),8,14 tetraen 17 one, Clinical Biochemistry, Spectrum Analysis, Mass, Biochemistry, Mass Spectrometry, infrared spectrophotometry, Structure-Activity Relationship, Steroids, Heterocyclic, Endocrinology, Isomerism, Support, Non-U.S. Gov't, Estrenes, Molecular Biology, nuclear magnetic resonance spectroscopy, structure activity relation, Pharmacology, dyes, reagents, indicators, markers and buffers, Organic Chemistry, article, estrane derivative, 1,6-dithiabenz(3,4)estra-3,5(10),8,14-tetraen-17-one, Indicators and Reagents, 1,6-dithiabenz(3,4)homoestra-3,5(10),8,14-tetraen-17-one, 1,6 dithiabenz(3,4)homoestra 3,5(10),8,14 tetraen 17 one

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb9e02696a923ee7ad82ae387baf8372
https://doi.org/10.1016/0039-128x(82)90073-3

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المؤلفون: Ramadas, S.R., Srinivasan, P.S.

المصدر: Steroids. 30:213-222

مصطلحات موضوعية: 3 thia a norestra 1,5(10),6,8,14 pentaen 17beta ol, steroidogenesis, isomerism, heterocyclic steroid, in vitro study, infrared spectrometry, Magnetic Resonance Spectroscopy, synthesis, Clinical Biochemistry, Heterocyclic steroids, Spectrum Analysis, Mass, Biochemistry, Medicinal chemistry, 3 thia a norestra 1,5(10),8,14 tetraen 17beta ol, Steroids, Heterocyclic, Endocrinology, Methods, spectrophotometry, Estrenes, Molecular Biology, mass spectrometry, nuclear magnetic resonance spectroscopy, Pharmacology, Chemistry, Organic Chemistry, drug identification, article, methodology, drug analysis, technique, theoretical study, estrane derivative, drug structure, nuclear magnetic resonance, ultraviolet spectrophotometry, drug synthesis

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https://doi.org/10.1016/0039-128x(77)90083-6

المؤلفون: S Padmanabhan, S. R. Ramadas

المصدر: Steroids. 33(2)

مصطلحات موضوعية: in vitro study, infrared spectrometry, Chemical Phenomena, Clinical Biochemistry, Heterocyclic steroids, Stereoisomerism, 7 methyl 2 phenyl 3 oxa a nor 14beta estra 1,5(10),6,8 tetraen 17beta ol, Biochemistry, Endocrinology, Heterocyclic Compounds, Methods, Organic chemistry, 17alpha hydroxy 7 methyl 2 phenyl a nor 14beta estra 1,5(10),6,8 tetraen 3 one, Estrenes, Molecular Biology, mass spectrometry, Benzofurans, Pharmacology, Chemistry, Organic Chemistry, drug identification, Total synthesis, drug analysis, theoretical study, drug structure, nuclear magnetic resonance, ultraviolet spectrophotometry, drug synthesis, 4,5,6,7 tetrahydro 6 methyl 4 oxo 2 phenylbenzofuran, Norsteroids

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2105dcb035bd409c247b0a4efb835d3f
https://pubmed.ncbi.nlm.nih.gov/462490

المؤلفون: Ramadas, S.R., Chandrakumar, N.S.

المصدر: IndraStra Global.

مصطلحات موضوعية: heterocyclic steroid, in vitro study, infrared spectrometry, Magnetic Resonance Spectroscopy, drug analysis, theoretical study, drug structure, nuclear magnetic resonance, Chemistry, Steroids, Heterocyclic, a nor 3,7 dithiaestra 1,5(10),8,14 tetraen 17 ol, drug synthesis, Support, Non-U.S. Gov't, Oxidation-Reduction, mass spectrometry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=issn23813652::43860aa2ca62b842f9a78883150f4dd0
https://igi.indrastra.com/items/show/67212

المؤلفون: Sara Cravo, Madalena Pinto, Artur M. S. Silva, Tida Dethoup, War War May Zin, José Alberto Pereira, Anake Kijjoa, Suradet Buttachon, Carla Fernandes, Nazim Sekeroglu, Luís Gales

المساهمون: CIIMAR - Centro Interdisciplinar de Investigação Marinha e Ambiental

المصدر: Marine Drugs
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Marine Drugs, Vol 14, Iss 7, p 136 (2016)
Marine Drugs; Volume 14; Issue 7; Pages: 136

مصطلحات موضوعية: 0301 basic medicine, Antifungal Agents, aszonalenin, Neosartorya, Pharmaceutical Science, Neosartorya glabra, marine-derived fungus, Mycale sp, cyclotetrapeptides, sartoryglabramides A and B, diketopiperazines, fellutanine A epoxide, Trichophyton rubrum, (11ar)2,3 dihydro 1h pyrrolo[2,1 c][1,4]benzodiazepine 5,11(10h,11ah) dione, cyclotetrapeptide, X ray analysis, 01 natural sciences, Aspergillus fumigatus, Indole Alkaloids, chemistry.chemical_compound, Benzodiazepines, antibacterial activity, Ergosterol, Drug Discovery, Candida albicans, Amino Acids, Pharmacology, Toxicology and Pharmaceutics (miscellaneous), lcsh:QH301-705.5, acetic acid ethyl ester, chemistry.chemical_classification, ergosterol 5,8 endoperoxide, biology, stereochemistry, diketopiperzine, helvolic acid, Stereoisomerism, structure analysis, Amino acid, unclassified drug, Anti-Bacterial Agents, Porifera, Biochemistry, ergosta 4,6,8(14),22 tetraen 3 one, Antibacterial activity, Oligopeptides, amino acid, spectroscopy, Staphylococcus aureus, high performance liquid chromatography, Stereochemistry, sartoryglabramide B, sartoryglabramide A, fungus culture, Diketopiperazines, Microbial Sensitivity Tests, minimum inhibitory concentration, 3 (1h indol 3 ylmethyl) 3, 4 dihydro 1h 1,4 benzodiazepine 2,5 dione, Article, 03 medical and health sciences, fellutanine A, isolation procedure, Escherichia coli, Animals, controlled study, takakiamide, nonhuman, Bacteria, 010405 organic chemistry, antifungal activity, fungal strain, Fungi, nucleotide sequence, fungal extract, marine species, biology.organism_classification, Yeast, 0104 chemical sciences, 030104 developmental biology, chemistry, lcsh:Biology (General), sponge (Porifera), Fusidic Acid

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