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1 |
Material Type: Artigo
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1-[5-(2-Fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]-N-methylmethanamine monofumarate (TAK-438), a novel and potent potassium-competitive acid blocker for the treatment of acid-related diseasesHori, Yasunobu ; Imanishi, Akio ; Matsukawa, Jun ; Tsukimi, Yasuhiro ; Nishida, Haruyuki ; Arikawa, Yasuyoshi ; Hirase, Keizo ; Kajino, Masahiro ; Inatomi, NobuhiroThe Journal of pharmacology and experimental therapeutics, 2010-10, Vol.335 (1), p.231-238 [Periódico revisado por pares]United StatesTexto completo disponível |
2 |
Material Type: Artigo
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1, 5-Benzoxathiepin Derivatives. II. Synthesis and Serotonin S2-Receptor-Blocking Activity of Aminoalkyl-Substituted 3, 4-Dihydro-2H-1, 5-benzoxathiepin-3-ols and Related CompoundsSUGIHARA, HIROSADA ; MABUCHI, HIROSHI ; HIRATA, MINORU ; IMAMOTO, TETSUJI ; KAWAMATSU, YUTAKAChemical and Pharmaceutical Bulletin, 1987/05/25, Vol.35(5), pp.1930-1952 [Periódico revisado por pares]Tokyo: The Pharmaceutical Society of JapanTexto completo disponível |
3 |
Material Type: Artigo
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1, 5-Benzoxathiepin Derivatives. III. Optical Resolution of Methyl (±)-cis-3-Hydroxy-4-[3-(4-phenyl-1-piperazinyl)propyl]-3, 4-dihydro-2H-1, 5-benzoxathiepin-4-carboxylate Hydrochloride ((±)-CV-5197) with Selective 5-Hydroxytryptamine2(5-HT2)-Antagonistic ActivityKORI, Masakuni ; KAMIYA, Kazuhide ; KURIHARA, Etsuo ; SUGIHARA, HirosadaChemical and Pharmaceutical Bulletin, 1991/04/25, Vol.39(4), pp.922-926 [Periódico revisado por pares]Tokyo: The Pharmaceutical Society of JapanTexto completo disponível |
4 |
Material Type: Artigo
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1-(5-Carboxyindazol-1-yl)propan-2-ones as dual inhibitors of cytosolic phospholipase A 2 α and fatty acid amide hydrolase: bioisosteric replacement of the carboxylic acid moietyAlthaus, Jan ; Hake, Theresa ; Hanekamp, Walburga ; Lehr, MatthiasJournal of enzyme inhibition and medicinal chemistry, 2016-11, Vol.31 (sup1), p.131-140 [Periódico revisado por pares]EnglandTexto completo disponível |
5 |
Material Type: magazinearticle
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1,102 poundsThe New York times upfront, 2020-02, Vol.152 (9), p.4Scholastic, IncTexto completo disponível |
6 |
Material Type: Artigo
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1,1′-Disubstituted Ferrocenes as Molecular Hinges in Mono- and Bivalent Dopamine Receptor LigandsHuber, Daniela ; Hübner, Harald ; Gmeiner, PeterJournal of medicinal chemistry, 2009-11, Vol.52 (21), p.6860-6870 [Periódico revisado por pares]United States: American Chemical SocietyTexto completo disponível |
7 |
Material Type: Artigo
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1,2,3- dl-Tricarboxycyclopentene-1 and other inhibitors of cis-aconitaseGawron, Oscar ; Birckbichler, Paul J.Archives of biochemistry and biophysics, 1971-12, Vol.147 (2), p.772-780 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
8 |
Material Type: Artigo
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1,25-dihydroxyvitamin D radioreceptor assay using bovine mammary gland receptor and non-high performance liquid chromatographic purificationWATANABE, Y ; KUBOTA, T ; SUZUMURA, E ; SUZUKI, T ; YONEZAWA, M ; ISHIGAMI, T ; ICHIKAWA, M ; SEINO, YClinica chimica acta, 1994-03, Vol.225 (2), p.187-194 [Periódico revisado por pares]Shannon: ElsevierTexto completo disponível |
9 |
Material Type: Artigo
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1,25-Dihydroxyvitamin D3 induces 25-hydroxyvitamin D3-24-hydroxylase in a cultured monkey kidney cell line (LLC-MK2) apparently deficient in the high affinity receptor for the hormoneChandler, J S ; Chandler, S K ; Pike, J W ; Haussler, M RThe Journal of biological chemistry, 1984-02, Vol.259 (4), p.2214-2222 [Periódico revisado por pares]Bethesda, MD: Elsevier IncTexto completo disponível |
10 |
Material Type: Artigo
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1,25-Dihydroxyvitamin D3 Negatively Regulates the Inflammatory Response to Porcine Epidemic Diarrhea Virus Infection by Inhibiting NF-κB and JAK/STAT Signaling Pathway in IPEC-J2 Porcine Epithelial CellsYang, Jiwen ; Chen, Daiwen ; Tian, Gang ; Mao, Xiangbing ; He, Jun ; Zheng, Ping ; Yu, Jie ; Luo, Yuheng ; Luo, Junqiu ; Huang, Zhiqing ; Wu, Aimin ; Yan, Hui ; Yu, BingInternational journal of molecular sciences, 2022-09, Vol.23 (18), p.10603 [Periódico revisado por pares]Basel: MDPI AGTexto completo disponível |