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Archiv Der Pharmazie|April 1, 1991
[Thiophene as a structural element of physiologically active compounds. 19. The synthesis of substituted (6H-thieno[2,3-b]pyrrol-4-yl)phenylmethanones]D Binder, H Schnait, F Rovenszky, et al.
Archiv Der Pharmazie|April 1, 1991
Synergistic inhibition of aminopeptidase B by penicillamine or cysteine and metallic saltsR Herranz, M T García-López, C Pérez
Archiv Der Pharmazie|November 1, 2008
Design and synthesis of novel benzopyran-2-one derivatives of expected antimicrobial activity through DNA gyrase-B inhibitionGhaneya S Hassan, Nahla A Farag, Gehan H Hegazy, et al.
Archiv Der Pharmazie|August 1, 1991
Synthesis of 5'-N-(alpha-amino-beta-mercaptoacyl)amino-5'-deoxynucleosides as potential antiviral compoundsR Herranz, J Castro-Pichel, M T García-López, et al.
Archiv Der Pharmazie|April 4, 2007
N-(4-(4-(2-Halogenophenyl)piperazin-1-yl)butyl) substituted cinnamoyl amide derivatives as dopamine D2 and D3 receptor ligandsOliver Saur, Anneke E Hackling, Sylvie Perachon, et al.
Archiv Der Pharmazie|September 13, 2007
Synthesis and in-vitro activity of novel 1beta-methylcarbapenems having spiro[2,4]heptane moietiesHyeong Beom Park, Nam Hyun Jo, Joon Hee Hong, et al.
Archiv Der Pharmazie|August 11, 2020
Reprogramming of antibiotics to combat antimicrobial resistanceKashyap K Dubey, Indu, Manisha Sharma
Archiv Der Pharmazie|August 8, 2020
Determination of the inhibition profiles of pyrazolyl-thiazole derivatives against aldose reductase and α-glycosidase and molecular docking studiesYeliz Demir, Parham Taslimi, Ümit M Koçyiğit, et al.
Archiv Der Pharmazie|March 31, 2021
Design, synthesis, docking, ADMET profile, and anticancer evaluations of novel thiazolidine-2,4-dione derivatives as VEGFR-2 inhibitorsKhaled El-Adl, Helmy Sakr, Sanadelaslam S A El-Hddad, et al.
Archiv Der Pharmazie|April 5, 2023
Design, synthesis, α-glucosidase inhibition, pharmacokinetic, and cytotoxic studies of new indole-carbohydrazide-phenoxy-N-phenylacetamide derivativesHaleh Hamedifar, Maryam Mohammadi-Khanaposhtani, Maedeh Sherafati, et al.
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