Holzgrabe U - Search Results

1

The ameliorative effects of a phenolic derivative of Moringa oleifera leave against vanadium-induced neurotoxicity in mice.

Igado OO, Andrioli A, Azeez IA, Girolamo F, Errede M, Aina OO, Glaser J, Holzgrabe U, Bentivoglio M, Olopade JO. Igado OO, et al. Among authors: holzgrabe u. IBRO Rep. 2020 Jul 12;9:164-182. doi: 10.1016/j.ibror.2020.07.004. eCollection 2020 Dec. IBRO Rep. 2020. PMID: 32803016 Free PMC article.

2

Antileishmanial and cytotoxic compounds from Valeriana wallichii and identification of a novel nepetolactone derivative.

Glaser J, Schultheis M, Moll H, Hazra B, Holzgrabe U. Glaser J, et al. Among authors: holzgrabe u. Molecules. 2015 Apr 1;20(4):5740-53. doi: 10.3390/molecules20045740. Molecules. 2015. PMID: 25834987 Free PMC article.

3

Anti-Schistosomal Activity of Cinnamic Acid Esters: Eugenyl and Thymyl Cinnamate Induce Cytoplasmic Vacuoles and Death in Schistosomula of Schistosoma mansoni.

Glaser J, Schurigt U, Suzuki BM, Caffrey CR, Holzgrabe U. Glaser J, et al. Among authors: holzgrabe u. Molecules. 2015 Jun 12;20(6):10873-83. doi: 10.3390/molecules200610873. Molecules. 2015. PMID: 26076109 Free PMC article.

4

Cinnamic Acid Bornyl Ester Derivatives from Valeriana wallichii Exhibit Antileishmanial In Vivo Activity in Leishmania major-Infected BALB/c Mice.

Masic A, Valencia Hernandez AM, Hazra S, Glaser J, Holzgrabe U, Hazra B, Schurigt U. Masic A, et al. Among authors: holzgrabe u. PLoS One. 2015 Nov 10;10(11):e0142386. doi: 10.1371/journal.pone.0142386. eCollection 2015. PLoS One. 2015. PMID: 26554591 Free PMC article.

5

Isolation of a novel compound (MIMO2) from the methanolic extract of Moringa oleifera leaves: protective effects against vanadium-induced cytotoxity.

Igado OO, Glaser J, Ramos-Tirado M, Bankoğlu EE, Atiba FA, Holzgrabe U, Stopper H, Olopade JO. Igado OO, et al. Among authors: holzgrabe u. Drug Chem Toxicol. 2018 Jul;41(3):249-258. doi: 10.1080/01480545.2017.1366504. Epub 2017 Sep 19. Drug Chem Toxicol. 2018. PMID: 28925291

6

Antileishmanial lead structures from nature: analysis of structure-activity relationships of a compound library derived from caffeic Acid bornyl ester.

Glaser J, Schultheis M, Hazra S, Hazra B, Moll H, Schurigt U, Holzgrabe U. Glaser J, et al. Among authors: holzgrabe u. Molecules. 2014 Jan 27;19(2):1394-410. doi: 10.3390/molecules19021394. Molecules. 2014. PMID: 24473204 Free PMC article.

7

Anticancer effects of NSC‑631570 (Ukrain) in head and neck cancer cells: In vitro analysis of growth, invasion, angiogenesis and gene expression.

Herrmann R, Skaf J, Roller J, Polednik C, Holzgrabe U, Schmidt M. Herrmann R, et al. Among authors: holzgrabe u. Oncol Rep. 2020 Jan;43(1):282-295. doi: 10.3892/or.2019.7416. Epub 2019 Nov 25. Oncol Rep. 2020. PMID: 31789425

8

Mapping the pharmaceutical design space by amorphous ionic liquid strategies.

Wiest J, Saedtler M, Balk A, Merget B, Widmer T, Bruhn H, Raccuglia M, Walid E, Picard F, Stopper H, Dekant W, Lühmann T, Sotriffer C, Galli B, Holzgrabe U, Meinel L. Wiest J, et al. Among authors: holzgrabe u. J Control Release. 2017 Dec 28;268:314-322. doi: 10.1016/j.jconrel.2017.10.040. Epub 2017 Oct 31. J Control Release. 2017. PMID: 29097303

9

Stabilization of Delphinidin in Complex with Sulfobutylether-β-Cyclodextrin Allows for Antinociception in Inflammatory Pain.

Sauer RS, Krummenacher I, Bankoglu EE, Yang S, Oehler B, Schöppler F, Mohammadi M, Güntzel P, Ben-Kraiem A, Holzgrabe U, Stopper H, Broscheit JA, Braunschweig H, Roewer N, Brack A, Rittner HL. Sauer RS, et al. Among authors: holzgrabe u. Antioxid Redox Signal. 2021 Jun 1;34(16):1260-1279. doi: 10.1089/ars.2019.7957. Epub 2020 Nov 9. Antioxid Redox Signal. 2021. PMID: 32977733

10

Structure-activity relationships in a series of bisquaternary bisphthalimidine derivatives modulating the muscarinic M(2)-receptor allosterically.

Botero Cid HM, Tränkle C, Baumann K, Pick R, Mies-Klomfass E, Kostenis E, Mohr K, Holzgrabe U. Botero Cid HM, et al. Among authors: holzgrabe u. J Med Chem. 2000 Jun 1;43(11):2155-64. doi: 10.1021/jm991136e. J Med Chem. 2000. PMID: 10841794

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