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Toward the Asymmetric Synthesis of Cardenolides and Related Steroidal Systems: syn -S N 2' of Organometallics with C14-C17 Vinylepoxides.

• Authors : Millham AB; Department of Chemistry, Dartmouth College, Burke Laboratory, Hanover, New Hampshire 03755, United States.; Micalizio GC

Subjects: Biological Products* ; Triterpenes*; Cardenolides

• Source: Organic letters [Org Lett] 2022 Oct 07; Vol. 24 (39), pp. 7058-7061. Date of Electronic Publication: 2022 Sep 26.Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print-Electronic

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Toward the Asymmetric Synthesis of Cardenolides and Related Steroidal Systems: syn-SN2′ of Organometallics with C14–C17 Vinylepoxides.

• Authors : Millham, Adam B.; Micalizio, Glenn C.

• Source: Organic Letters; 10/7/2022, Vol. 24 Issue 39, p7058-7061, 4p

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Triple-Negative Breast Cancer Cells Exhibit Differential Sensitivity to Cardenolides from .

• Authors : Pederson, Petra J.; Cai, Shengxin; Carver, Chase

• Source: Journal of Natural Products; 7/24/2020, Vol. 83 Issue 7, p2269-2280, 12p

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Naturally Occurring Cardenolides Affecting Schistosoma mansoni.

• Authors : Keiser, Jennifer; Koch, Vanessa; Deckers, Anke

• Source: ACS Infectious Diseases; 7/10/2020, Vol. 6 Issue 7, p1922-1927, 6p

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Calosides A-F, Cardenolides from and Their Cytotoxic Activity.

• Authors : Nguyen, Mai T T; Nguyen, Khang D H; Dang, Phu H

• Source: Journal of Natural Products; 2/28/2020, Vol. 83 Issue 2, p385-391, 7p

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Potent Antagonists of RORγt, Cardenolides from Calotropis gigantea, Exhibit Discrepant Effects on the Differentiation of T Lymphocyte Subsets.

• Authors : Liu J; State Key Laboratory of Quality Research in Chinese Medicines, Macau Institute for Applied Research in Medicine and Health , Macau University of Science and Technology , Avenida Wai Long , Taipa , Macau 999078 , People's Republic of China.; Bai LP

Subjects: Calotropis/Calotropis/Calotropis/*chemistry ; Cardenolides/Cardenolides/Cardenolides/*pharmacology ; Cell Differentiation/Cell Differentiation/Cell Differentiation/*drug effects

• Source: Molecular pharmaceutics [Mol Pharm] 2019 Feb 04; Vol. 16 (2), pp. 798-807. Date of Electronic Publication: 2019 Jan 22.Publisher: American Chemical Society Country of Publication: United States NLM ID: 101197791 Publication Model: Print-Electronic

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Antiproliferative Cardenolides from the Aerial Parts of Pergularia tomentosa.

• Authors : Hosseini, Seyed Hamzeh; Masullo, Milena; Cerulli, Antonietta

• Source: Journal of Natural Products; Jan2019, Vol. 82 Issue 1, p74-79, 6p

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A Strategy for Total Synthesis of Complex Cardenolides.

• Authors : Deng W; Department of Chemistry, 516 Physical Sciences 1, University of California, Irvine, California 92697-2025.; Jensen MS

• Source: The Journal of organic chemistry [J Org Chem] 1996 Oct 04; Vol. 61 (20), pp. 6760-6761.Publisher: American Chemical Society Country of Publication: United States NLM ID: 2985193R Publication Model: Print Cited

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Inhibition of beef-brain and dog-heart (Na+ + k+) activated adenosine triphosphatase by carbon-3 branched cardenolides.

• Authors : Siebeneick HU; Hoffmann W

Subjects: Cardenolides/Cardenolides/Cardenolides/*pharmacology ; Sodium-Potassium-Exchanging ATPase/Sodium-Potassium-Exchanging ATPase/Sodium-Potassium-Exchanging ATPase/*antagonists & inhibitors; Animals

• Source: Journal of medicinal chemistry [J Med Chem] 1978 Dec; Vol. 21 (12), pp. 1310-2.Publisher: American Chemical Society Country of Publication: United States NLM ID: 9716531 Publication Model: Print Cited

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Steroids and related natural products. 94 Synthesis of toad venom cardenolides.

• Authors : Kamano Y; Pettit GR; Tozawa M

Subjects: Cardenolides/Cardenolides/Cardenolides/*chemical synthesis; Animals ; Bufonidae

• Source: The Journal of organic chemistry [J Org Chem] 1977 Mar 04; Vol. 42 (5), pp. 906-8.Publisher: American Chemical Society Country of Publication: United States NLM ID: 2985193R Publication Model: Print Cited

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