المؤلفون: Hansen, Stinne Wessel, Erichsen, Mette Norman, Fu, Bingru, Bjørn-Yoshimoto, Walden Emil, Abrahamsen, Bjarke, Hansen, Jacob Christian, Jensen, Anders A., Bunch, Lennart

المصدر: Hansen , S W , Erichsen , M N , Fu , B , Bjørn-Yoshimoto , W E , Abrahamsen , B , Hansen , J C , Jensen , A A & Bunch , L 2016 , ' Identification of a New Class of Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitors Followed by a Structure-Activity-Relationship Study ' , Journal of Medicinal Chemistry , vol. 59 , no. 19 , pp. 8757-8770 . https://doi.org/10.1021/acs.jmedchem.6b01058

الاتاحة: https://researchprofiles.ku.dk/da/publications/identification-of-a-new-class-of-selective-excitatory-amino-acid-transporter-subtype-1-eaat1-inhibitors-followed-by-a-structureactivityrelationship-study(0ac1b4d8-bff2-417f-ba1d-c32e752aceb3).html
https://doi.org/10.1021/acs.jmedchem.6b01058

المؤلفون: Erichsen, Mette Norman

المصدر: Erichsen , M N 2011 , Design and synthesis of subtype selective ligands for the human excitatory amino acid transporters (EAATs) and design and synthesis of novel selective phosphodiesterase 10A (PDE10A) inhibitors . Det Farmaceutiske Fakultet , København . < https://diskurs.kb.dk/item/diskurs:19192:6 >

مصطلحات موضوعية: /dk/atira/pure/core/keywords/TheFacultyOfPharmaceuticalSciences, Former Faculty of Pharmaceutical Sciences

الاتاحة: https://curis.ku.dk/portal/da/publications/design-and-synthesis-of-subtype-selective-ligands-for-the-human-excitatory-amino-acid-transporters-eaats-and-design-and-synthesis-of-novel-selective-phosphodiesterase-10a-pde10a-inhibitors(b947f860-4fc7-4337-b140-7bac187e053d).html
https://diskurs.kb.dk/item/diskurs:19192:6

المؤلفون: Erichsen, Mette Norman, Hansen, J, Artacho Ruiz, Jose, Demmer, Charles Sylvain, Abrahamsen, Bjarke, Bastlund, Jesper F, Bundgaard, C, Jensen, Anders A., Bunch, Lennart

المصدر: Erichsen , M N , Hansen , J , Artacho Ruiz , J , Demmer , C S , Abrahamsen , B , Bastlund , J F , Bundgaard , C , Jensen , A A & Bunch , L 2014 , ' Probing for improved potency and in vivo bioavailability of excitatory amino acid transporter subtype 1 inhibitors UCPH-101 and UCPH-102: Design, synthesis and pharmacological evaluation of substituted 7-biphenyl analogs ' , Neurochemical Research , vol. 39 , no. 10 , pp. 1964-1979 . https://doi.org/10.1007/s11064-014-1264-8

الاتاحة: https://researchprofiles.ku.dk/da/publications/probing-for-improved-potency-and-in-vivo-bioavailability-of-excitatory-amino-acid-transporter-subtype-1-inhibitors-ucph101-and-ucph102-design-synthesis-and-pharmacological-evaluation-of-substituted-7biphenyl-analogs(252ec095-2e5d-446e-bcf7-9ee366445c70).html
https://doi.org/10.1007/s11064-014-1264-8

المؤلفون: Abrahamsen, Bjarke, Schneider, Nicole, Erichsen, Mette Norman, Huynh, Tri Hien Viet, Fahlke, Christoph, Bunch, Lennart, Jensen, Anders A.

المصدر: Abrahamsen , B , Schneider , N , Erichsen , M N , Huynh , T H V , Fahlke , C , Bunch , L & Jensen , A A 2013 , ' Allosteric modulation of an excitatory amino acid transporter: The subtype-selective inhibitor UCPH-101 exerts sustained inhibition of EAAT1 through an intramonomeric site in the trimerization domain ' , Journal of Neuroscience , vol. 33 , no. 3 , pp. 1068-1087 . https://doi.org/10.1523/JNEUROSCI.3396-12.2013

الاتاحة: https://researchprofiles.ku.dk/da/publications/allosteric-modulation-of-an-excitatory-amino-acid-transporter-the-subtypeselective-inhibitor-ucph101-exerts-sustained-inhibition-of-eaat1-through-an-intramonomeric-site-in-the-trimerization-domain(2e0f3861-2afd-4479-a1ef-26f0cd3b75a7).html
https://doi.org/10.1523/JNEUROSCI.3396-12.2013

المؤلفون: Erichsen, Mette Norman, Huynh, Tri Hien Viet, Abrahamsen, Bjarke, Bastlund, Jesper Frank, Bundgaard, Christoffer, Monrad, Olja, Bekker-Jensen, Anders, Nielsen, Christina Wøhlk, Frydenvang, Karla Andrea, Jensen, Anders Asbjørn, Bunch, Lennart

المصدر: Erichsen , M N , Huynh , T H V , Abrahamsen , B , Bastlund , J F , Bundgaard , C , Monrad , O , Bekker-Jensen , A , Nielsen , C W , Frydenvang , K A , Jensen , A A & Bunch , L 2010 , ' Structure-activity relationship study of first selective inhibitor of excitatory amino acid transporter subtype 1 : 2-amino-4-(4-methoxyphenyl)-7-(naphthalen-1-yl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile (UCPH-101) ' , Journal of Medicinal Chemistry , vol. 53 , no. 19 , pp. 7180–7191 . https://doi.org/10.1021/jm1009154

مصطلحات موضوعية: /dk/atira/pure/core/keywords/TheFacultyOfPharmaceuticalSciences, Former Faculty of Pharmaceutical Sciences

الاتاحة: https://researchprofiles.ku.dk/da/publications/structureactivity-relationship-study-of-first-selective-inhibitor-of-excitatory-amino-acid-transporter-subtype-1(96e7f264-c160-4dec-809f-d3392d8ae406).html
https://doi.org/10.1021/jm1009154

المؤلفون: Erichsen, Mette Norman

مصطلحات الفهرس: person

URL: https://curis.ku.dk/portal/da/persons/mette-norman-erichsen(6cec93b0-3a04-468d-88a2-0a65570cfb7a).html