المؤلفون: Gerardo Burton, Valeria Carolina Edelsztein, Pablo H. Di Chenna, Fernando Javier Duran, Mario David Martinez

مصطلحات موضوعية: Steric effects, Azasteroids, Stereochemistry, medicine.medical_treatment, Clinical Biochemistry, Gene Expression, Biochemistry, Steroid, Secosteroid, chemistry.chemical_compound, Endocrinology, Genes, Reporter, Chlorocebus aethiops, medicine, Animals, Humans, Receptor, Luciferases, Promoter Regions, Genetic, Molecular Biology, Progesterone, Pharmacology, 19-Hydroxypregnane, Chemistry, Organic Chemistry, Ciencias Químicas, Pregnanes, medicine.anatomical_structure, Química Orgánica, Cyclization, Gestagenic activity, Yield (chemistry), 6-Azaprogesterone, COS Cells, Pregnenolone, Receptors, Progesterone, Nucleus, CIENCIAS NATURALES Y EXACTAS, medicine.drug

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4af7fe5d71fa3a6d8a2082515cb064b
http://www.sciencedirect.com/science/article/pii/S0039128X12002887

المؤلفون: Martínez, M.D., Edelsztein, V.C., Durán, F.J., Di Chenna, P.H., Burton, G.

مصطلحات موضوعية: 19-Hydroxypregnane, 6-Azaprogesterone, Azasteroids, Gestagenic activity, 18 hydroxy 20 oxosteroid, 18 hydroxydeoxycorticosterone, 18 hydroxyprogesterone, 19 hydroxy 3 oxosteroid, 19 hydroxy 6 (tert butoxycarbonyl) 6 aza 4 pregnene 3,20 dione, 19 hydroxy 6 azaprogesterone, 19 hydroxy 6 azasteroid, 3beta tert butyldimethylsilyloxy 19 formyloxy 6 aza 5 pregnen 20 one, 3beta tert butyldimethylsilyloxy 6 (tert butoxycarbonyl) 19 formyloxy 6 aza 4 pregnen 20 one, 3beta tert butyldimethylsilyloxy 7 azido 19 formyloxy 6 nor 5,7 secopregnane 5,20 dione, 3beta,19 dihydroxy 6 (tert butoxycarbonyl) 6 aza 4 pregnen 20 one, 6 azaprogesterone, azasteroid, gestagen, manganese dioxide, pregnenolone, progesterone receptor, secosteroid, unclassified drug, acylation, animal cell, article, chemical bond, controlled study, cyclization, drug structure

Relation: http://hdl.handle.net/20.500.12110/paper_0039128X_v78_n1_p34_Martinez

الاتاحة: https://hdl.handle.net/20.500.12110/paper_0039128X_v78_n1_p34_Martinez

المؤلفون: Martinez, Mario David, Edelsztein, Valeria Carolina, Duran, Fernando Javier, Di Chenna, Pablo Hector, Burton, Gerardo

مصطلحات موضوعية: Azasteroids, 6-Azaprogesterone, 19-Hydroxypregnane, Gestagenic Activity, https://purl.org/becyt/ford/1.4, https://purl.org/becyt/ford/1

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0039128X12002887; http://hdl.handle.net/11336/18679; Martinez, Mario David; Edelsztein, Valeria Carolina; Duran, Fernando Javier; Di Chenna, Pablo Hector; Burton, Gerardo; Synthesis of 6-azaprogesterone and 19-hydroxy-6-azasteroids; Elsevier Science Inc; Steroids; 78; 1; 1-2013; 34-37; CONICET Digital; CONICET

الاتاحة: http://hdl.handle.net/11336/18679

المؤلفون: Edelsztein, Valeria Carolina, Durán, Fernando Javier, Di Chenna, Pablo Héctor, Burton, Gerardo

مصطلحات موضوعية: 19-Hydroxypregnane, 6-Azaprogesterone, Azasteroids, Gestagenic activity, 18 hydroxy 20 oxosteroid, 18 hydroxydeoxycorticosterone, 18 hydroxyprogesterone, 19 hydroxy 3 oxosteroid, 19 hydroxy 6 (tert butoxycarbonyl) 6 aza 4 pregnene 3,20 dione, 19 hydroxy 6 azaprogesterone, 19 hydroxy 6 azasteroid, 3beta tert butyldimethylsilyloxy 19 formyloxy 6 aza 5 pregnen 20 one, 3beta tert butyldimethylsilyloxy 6 (tert butoxycarbonyl) 19 formyloxy 6 aza 4 pregnen 20 one, 3beta tert butyldimethylsilyloxy 7 azido 19 formyloxy 6 nor 5,7 secopregnane 5,20 dione, 3beta,19 dihydroxy 6 (tert butoxycarbonyl) 6 aza 4 pregnen 20 one, 6 azaprogesterone, azasteroid, gestagen, manganese dioxide, pregnenolone, progesterone receptor, secosteroid, unclassified drug, acylation, animal cell, article, chemical bond, controlled study, cyclization, drug structure

Relation: https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0039128X_v78_n1_p34_Martinez; http://hdl.handle.net/20.500.12110/paper_0039128X_v78_n1_p34_Martinez

الاتاحة: https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0039128X_v78_n1_p34_Martinez
https://hdl.handle.net/20.500.12110/paper_0039128X_v78_n1_p34_Martinez