المؤلفون: Carlos A. Bueno, Franco M. Salinas, L. Vazquez, Laura E. Alché, Flavia M. Michelini

المصدر: Heliyon, Vol 9, Iss 10, Pp e20148- (2023)

مصطلحات موضوعية: Human respiratory syncytial virus, Synthetic stigmastanes, Antiviral, Anti-inflammatory, Science (General), Q1-390, Social sciences (General), H1-99

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2405844023073565; https://doaj.org/toc/2405-8440

URL الوصول: https://doaj.org/article/9334d83a17af405eb05ea16388865c3f

المؤلفون: Tseme Wandji, Nadine, Bitchagno, Gabin Thierry M., Mawabo Kamga, Isabelle, Tchamgoue, Joseph, Nkenfou, Celine Nguefeu, Lenta, Bruno Ndjakou, Sewald, Norbert, Kouam, Simeon Fogue

مصطلحات موضوعية: Vernonia kotschyana, Asteraceae, stigmastanes, structure elucidation, chemophenetic significance, antibacterial activity, ddc:540

Relation: info:eu-repo/semantics/altIdentifier/issn/1420-3049; info:eu-repo/semantics/altIdentifier/wos/001032927700001; info:eu-repo/semantics/altIdentifier/pmid/37446939; https://nbn-resolving.org/urn:nbn:de:0070-pub-29807167; https://pub.uni-bielefeld.de/record/2980716; https://pub.uni-bielefeld.de/download/2980716/2980718

الاتاحة: https://nbn-resolving.org/urn:nbn:de:0070-pub-29807167
https://pub.uni-bielefeld.de/record/2980716
https://pub.uni-bielefeld.de/download/2980716/2980718

المؤلفون: Nadine Tseme Wandji, Gabin Thierry M. Bitchagno, Isabelle Mawabo Kamga, Joseph Tchamgoue, Celine Nguefeu Nkenfou, Bruno Ndjakou Lenta, Norbert Sewald, Simeon Fogue Kouam

المصدر: Molecules; Volume 28; Issue 13; Pages: 5278

مصطلحات موضوعية: Vernonia kotschyana, Asteraceae, stigmastanes, structure elucidation, chemophenetic significance, antibacterial activity

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Natural Products Chemistry; https://dx.doi.org/10.3390/molecules28135278

الاتاحة: https://doi.org/10.3390/molecules28135278

المؤلفون: Lydia R. Galagovsky, Fernando Alonso, Javier A. Ramírez, Sofía L. Acebedo

مصطلحات موضوعية: Stigmasterol, BIOACTIVITY, Chemistry, Stereochemistry, Otras Ciencias Químicas, Organic Chemistry, A-RING, Ciencias Químicas, AROMATIC STIGMASTANES, Biochemistry, chemistry.chemical_compound, Yield (chemistry), Drug Discovery, Organic chemistry, CIENCIAS NATURALES Y EXACTAS, Demethylation, BRASSINOSTEROIDS

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f802a438bd04a3588af394d8d05f3401
https://www.sciencedirect.com/science/article/pii/S0040402012004231

المؤلفون: Bueno, Carlos Alberto, Salinas, Franco Maximiliano, Vazquez, L., Alche, Laura Edith, Michelini, Flavia Mariana

مصطلحات موضوعية: ANTI-INFLAMMATORY, ANTIVIRAL, HUMAN RESPIRATORY SYNCYTIAL VIRUS, SYNTHETIC STIGMASTANES, https://purl.org/becyt/ford/1.6, https://purl.org/becyt/ford/1

وصف الملف: application/pdf

Relation: http://hdl.handle.net/11336/228347; CONICET Digital; CONICET

الاتاحة: http://hdl.handle.net/11336/228347

المؤلفون: Acebedo, S.L., Alonso, F., Ramírez, J.A., Galagovsky, L.R.

مصطلحات موضوعية: A-ring, Aromatic stigmastanes, Bioactivity, Brassinosteroids, 19 acetoxystigmasta 4,22 dien 3,6 dione, 19 nor 3,22,23 trihydroxystigmasta 1,3,5(10) triene 6 one, 19 norstigmasta 1(10),5,22 trien 3b ol, 19 norstigmasta 1,3,5(10) triene 3,22,23 triol, 19 norstigmasta 1,3,5(10),22 tetraen 3 ol, 3 hydroxystigmastane, 3beta acetoxy 19 norstigmasta 1(10),5,22 triene, 3beta acetoxy 5alpha bromo 6,19 epoxystigmast 22 ene, 3beta acetoxy 5alpha bromostigmast 22 en 6beta ol, 3beta acetoxy 5beta,6beta epoxystigmast 22 ene, 3beta acetoxystigmasta 5,22 dien 19 ol, 3beta,19 diacetoxystigmasta 5,22 diene, 9 acetoxystigmasta 5,22 dien 3beta ol, 9 nor 3 hydroxystigmasta 1,3,5(10),22 tetraen 6 one, aromatic compound, brassinosteroid, stigmasta 1,4,22 trien 3 one, stigmasta 3beta,22,23 triol (6 deoxo 28 homoteasterone), stigmasterol, unclassified drug, aromatization, article, demethylation, drug activity, hydrolysis, oxidation

Relation: http://hdl.handle.net/20.500.12110/paper_00404020_v68_n19_p3685_Acebedo

الاتاحة: https://hdl.handle.net/20.500.12110/paper_00404020_v68_n19_p3685_Acebedo

المؤلفون: Acebedo, Sofía Lorena, Alonso, Fernando, Ramirez, Javier Alberto, Galagovsky, Lydia Raquel

مصطلحات موضوعية: A-Ring, Aromatic Stigmastanes, Bioactivity, Brassinosteroids, https://purl.org/becyt/ford/1.4, https://purl.org/becyt/ford/1

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0040402012004231; http://hdl.handle.net/11336/69385; Acebedo, Sofía Lorena; Alonso, Fernando; Ramirez, Javier Alberto; Galagovsky, Lydia Raquel; Synthesis of aromatic stigmastanes: Application to the synthesis of aromatic analogs of brassinosteroids; Pergamon-Elsevier Science Ltd; Tetrahedron; 68; 19; 5-2012; 3685-3691; CONICET Digital; CONICET

الاتاحة: http://hdl.handle.net/11336/69385

المؤلفون: Acebedo, Sofìa Lorena, Ramirez, Javier Alberto

مصطلحات موضوعية: A-ring, Aromatic stigmastanes, Bioactivity, Brassinosteroids, 19 acetoxystigmasta 4,22 dien 3,6 dione, 19 nor 3,22,23 trihydroxystigmasta 1,3,5(10) triene 6 one, 19 norstigmasta 1(10),5,22 trien 3b ol, 19 norstigmasta 1,3,5(10) triene 3,22,23 triol, 19 norstigmasta 1,3,5(10),22 tetraen 3 ol, 3 hydroxystigmastane, 3beta acetoxy 19 norstigmasta 1(10),5,22 triene, 3beta acetoxy 5alpha bromo 6,19 epoxystigmast 22 ene, 3beta acetoxy 5alpha bromostigmast 22 en 6beta ol, 3beta acetoxy 5beta,6beta epoxystigmast 22 ene, 3beta acetoxystigmasta 5,22 dien 19 ol, 3beta,19 diacetoxystigmasta 5,22 diene, 9 acetoxystigmasta 5,22 dien 3beta ol, 9 nor 3 hydroxystigmasta 1,3,5(10),22 tetraen 6 one, aromatic compound, brassinosteroid, stigmasta 1,4,22 trien 3 one, stigmasta 3beta,22,23 triol (6 deoxo 28 homoteasterone), stigmasterol, unclassified drug, aromatization, article, demethylation, drug activity, hydrolysis, oxidation

Relation: https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v68_n19_p3685_Acebedo; http://hdl.handle.net/20.500.12110/paper_00404020_v68_n19_p3685_Acebedo

الاتاحة: https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v68_n19_p3685_Acebedo
https://hdl.handle.net/20.500.12110/paper_00404020_v68_n19_p3685_Acebedo